roebe 0.5.147

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Files changed (2891) hide show
  1. checksums.yaml +7 -0
  2. data/README.md +2982 -0
  3. data/bin/blinking_cursor +7 -0
  4. data/bin/browser +7 -0
  5. data/bin/colourized_tokenitor1 +7 -0
  6. data/bin/colourized_tokenitor2 +7 -0
  7. data/bin/colourized_tokenitor3 +7 -0
  8. data/bin/colourized_tokenitor4 +7 -0
  9. data/bin/colourized_tokenitor5 +7 -0
  10. data/bin/compare_these_two_directories +7 -0
  11. data/bin/create_file_skeleton +7 -0
  12. data/bin/create_my_directories +7 -0
  13. data/bin/create_wpa_supplicant_build_file +7 -0
  14. data/bin/create_zip +7 -0
  15. data/bin/custom_invoke +28 -0
  16. data/bin/delete_empty_files +7 -0
  17. data/bin/display_gcc_version +7 -0
  18. data/bin/do_a_google_search +7 -0
  19. data/bin/extract_gem_file +7 -0
  20. data/bin/fragment_maker +7 -0
  21. data/bin/generate_fstab_file +7 -0
  22. data/bin/handle_xorg_related_boot_phase +7 -0
  23. data/bin/hello_world +7 -0
  24. data/bin/in +7 -0
  25. data/bin/increment_application_version +7 -0
  26. data/bin/increment_application_version_then_push_the_gem +13 -0
  27. data/bin/install_all_registered_fonts +7 -0
  28. data/bin/install_my_addons +114 -0
  29. data/bin/interactive_file_creator +7 -0
  30. data/bin/java_compile_statically +11 -0
  31. data/bin/kill_firefox +7 -0
  32. data/bin/kill_palemoon +7 -0
  33. data/bin/konsole_title +7 -0
  34. data/bin/larrow +7 -0
  35. data/bin/log10 +7 -0
  36. data/bin/menugenerator +7 -0
  37. data/bin/modify_shebang_header +7 -0
  38. data/bin/openpdf1 +7 -0
  39. data/bin/openpdf2 +7 -0
  40. data/bin/openpdf3 +7 -0
  41. data/bin/openpdf4 +7 -0
  42. data/bin/openpdf5 +7 -0
  43. data/bin/openpdf6 +7 -0
  44. data/bin/openpdf7 +7 -0
  45. data/bin/openpdf8 +7 -0
  46. data/bin/openpdf9 +7 -0
  47. data/bin/passwords +7 -0
  48. data/bin/path_generator +7 -0
  49. data/bin/print_this_unicode_symbol +7 -0
  50. data/bin/quick_colour_test +13 -0
  51. data/bin/rarrow +7 -0
  52. data/bin/rdate +7 -0
  53. data/bin/remove_this_substring_from_all_files +7 -0
  54. data/bin/replace_space_with_underscore +7 -0
  55. data/bin/rfirefox +7 -0
  56. data/bin/rinstall2 +7 -0
  57. data/bin/roebe +7 -0
  58. data/bin/roebe_documentation +7 -0
  59. data/bin/roebeshell +11 -0
  60. data/bin/ruby_cat +7 -0
  61. data/bin/ruby_dhcpcd +7 -0
  62. data/bin/run +7 -0
  63. data/bin/rxinitrc +7 -0
  64. data/bin/set_alias_1 +7 -0
  65. data/bin/set_alias_10 +7 -0
  66. data/bin/set_alias_11 +7 -0
  67. data/bin/set_alias_12 +7 -0
  68. data/bin/set_alias_13 +7 -0
  69. data/bin/set_alias_14 +7 -0
  70. data/bin/set_alias_15 +7 -0
  71. data/bin/set_alias_2 +7 -0
  72. data/bin/set_alias_3 +7 -0
  73. data/bin/set_alias_4 +7 -0
  74. data/bin/set_alias_5 +7 -0
  75. data/bin/set_alias_6 +7 -0
  76. data/bin/set_alias_7 +7 -0
  77. data/bin/set_alias_8 +7 -0
  78. data/bin/set_alias_9 +7 -0
  79. data/bin/set_browser +7 -0
  80. data/bin/setpdf1 +7 -0
  81. data/bin/setpdf2 +7 -0
  82. data/bin/setpdf3 +7 -0
  83. data/bin/setpdf4 +7 -0
  84. data/bin/setpdf5 +7 -0
  85. data/bin/setpdf6 +7 -0
  86. data/bin/setpdf7 +7 -0
  87. data/bin/setpdf8 +7 -0
  88. data/bin/setpdf9 +7 -0
  89. data/bin/show_available_users +7 -0
  90. data/bin/show_ten_aliases +7 -0
  91. data/bin/simple_extractor +9 -0
  92. data/bin/start_lighty +7 -0
  93. data/bin/symlink_directories_from_that_directory_to_the_current_directory +7 -0
  94. data/bin/symlink_everything_from_that_directory_to_this_directory +7 -0
  95. data/bin/symlink_files_from_that_directory_to_the_current_directory +7 -0
  96. data/bin/take_screenshot +7 -0
  97. data/bin/to_binary +7 -0
  98. data/bin/tokenitor +7 -0
  99. data/bin/vim_paradise +7 -0
  100. data/bin/wlan +7 -0
  101. data/bin/word_count +7 -0
  102. data/bin/write_what_into +7 -0
  103. data/bin/yaml_check +7 -0
  104. data/doc/README.gen +2942 -0
  105. data/doc/add_ons_for_ruby/README.md +3 -0
  106. data/doc/add_ons_for_ruby/axlsx.md +60 -0
  107. data/doc/add_ons_for_ruby/cgi.md +16 -0
  108. data/doc/add_ons_for_ruby/falcon.md +0 -0
  109. data/doc/add_ons_for_ruby/fxruby.md +14 -0
  110. data/doc/add_ons_for_ruby/glimmer-libui.md +43 -0
  111. data/doc/add_ons_for_ruby/gosu.md +3 -0
  112. data/doc/add_ons_for_ruby/hexapdf.md +66 -0
  113. data/doc/add_ons_for_ruby/jruby.md +199 -0
  114. data/doc/add_ons_for_ruby/kramdown.md +34 -0
  115. data/doc/add_ons_for_ruby/mail.md +51 -0
  116. data/doc/add_ons_for_ruby/opal.md +34 -0
  117. data/doc/add_ons_for_ruby/padrino.md +4 -0
  118. data/doc/add_ons_for_ruby/prawn.md +30 -0
  119. data/doc/add_ons_for_ruby/rack.md +214 -0
  120. data/doc/add_ons_for_ruby/roda.md +6 -0
  121. data/doc/add_ons_for_ruby/sequel.md +51 -0
  122. data/doc/add_ons_for_ruby/tty_box.md +28 -0
  123. data/doc/add_ons_for_ruby/watir.md +30 -0
  124. data/doc/add_ons_for_ruby/whois.md +15 -0
  125. data/doc/core/array.md +65 -0
  126. data/doc/core/blocks.md +38 -0
  127. data/doc/core/enumerator.md +15 -0
  128. data/doc/core/io_console.md +15 -0
  129. data/doc/core/open_uri.md +29 -0
  130. data/doc/core/pp.md +29 -0
  131. data/doc/core/process.md +21 -0
  132. data/doc/core/rbconfig.md +39 -0
  133. data/doc/core/regex.md +23 -0
  134. data/doc/core/rubyvm.md +4 -0
  135. data/doc/core/symbols.md +47 -0
  136. data/doc/core/tempfile.md +34 -0
  137. data/doc/core/tracepoint.md +7 -0
  138. data/doc/core/unicode.md +5 -0
  139. data/doc/core/unprintable_characters.md +17 -0
  140. data/doc/deprecations.md +10 -0
  141. data/doc/diamond_shell_tutorial.cgi +589 -0
  142. data/doc/linux_may_have_issues.md +92 -0
  143. data/doc/misc/how_to_publish.md +49 -0
  144. data/doc/misc/the_initialize_method.md +2 -0
  145. data/doc/misc/the_perfect_book.md +14 -0
  146. data/doc/old_tutorial/README.md +7 -0
  147. data/doc/old_tutorial/old_diashell_tutorial.cgi +2105 -0
  148. data/doc/roebeshell/CONFIGURATION_FOR_THE_ROEBE_SHELL.md +381 -0
  149. data/doc/roebeshell/MANIFESTO_FOR_THE_ROEBE_SHELL_COMPONENT.md +391 -0
  150. data/doc/roebeshell/PHILOSOPHY_OF_THE_ROEBE_SHELL.md +64 -0
  151. data/doc/ruby_on_rails_tutorial/data_types_for_rails_migrations.md +11 -0
  152. data/doc/ruby_on_rails_tutorial/ruby_on_rails_tutorial.cgi +404 -0
  153. data/doc/sinatra_tutorial/sinatra_tutorial.cgi +7 -0
  154. data/doc/sinatra_tutorial/sinatra_tutorial.rb +930 -0
  155. data/doc/sinatra_tutorial/sinatra_tutorial.sinatra +56 -0
  156. data/doc/statistics/statistics.md +94 -0
  157. data/doc/the_ruby_philosophy/the_ruby_philosophy.md +6 -0
  158. data/doc/todo/todo_for_the_roebe_project.md +1 -0
  159. data/doc/todo/todo_for_the_roebe_project_on_windows.md +4 -0
  160. data/doc/todo/todo_for_the_roebe_shell.md +759 -0
  161. data/examples/README.md +4 -0
  162. data/examples/date_and_time/is_this_day_part_of_that_range.rb +45 -0
  163. data/examples/misc/argv_encoding_test.rb +38 -0
  164. data/examples/misc/arrays/center_two_arrays.rb +24 -0
  165. data/examples/misc/loops/display_coloured_vertical_bars.rb +10 -0
  166. data/examples/rack/README.md +2 -0
  167. data/examples/rack/all_in_one_rack_example.rb +241 -0
  168. data/examples/rack/hello_world_in_rack.rb +37 -0
  169. data/examples/recursion/README.md +2 -0
  170. data/examples/recursion/quadratic_sum_of_a_number.rb +23 -0
  171. data/examples/recursion/reverse_the_string.rb +31 -0
  172. data/examples/recursion/shift_highest_value.rb +30 -0
  173. data/examples/recursion/shuffle_sort_string.rb +35 -0
  174. data/examples/rmagick/001_axes.rb +68 -0
  175. data/examples/rmagick/002_basic_2D_canvas.rb +29 -0
  176. data/examples/rmagick/003_a_walking_duck.rb +42 -0
  177. data/examples/rmagick/004_black_rectangle_with_red_border.rb +37 -0
  178. data/examples/rmagick/A_WALKING_DUCK.gif +0 -0
  179. data/examples/rmagick/foobar.png +0 -0
  180. data/examples/tty_box/all_in_one.rb +33 -0
  181. data/lib/roebe/autoinclude.rb +4 -0
  182. data/lib/roebe/autoinclude_encoding.rb +11 -0
  183. data/lib/roebe/autoinclude_open.rb +3 -0
  184. data/lib/roebe/base/base.rb +25 -0
  185. data/lib/roebe/base/chdir.rb +48 -0
  186. data/lib/roebe/base/colours.rb +600 -0
  187. data/lib/roebe/base/commandline_arguments.rb +96 -0
  188. data/lib/roebe/base/constants.rb +25 -0
  189. data/lib/roebe/base/copy.rb +72 -0
  190. data/lib/roebe/base/editor.rb +18 -0
  191. data/lib/roebe/base/encoding.rb +54 -0
  192. data/lib/roebe/base/env.rb +22 -0
  193. data/lib/roebe/base/esystem.rb +99 -0
  194. data/lib/roebe/base/home_directory_of_user_x.rb +27 -0
  195. data/lib/roebe/base/is_on_roebe.rb +22 -0
  196. data/lib/roebe/base/misc.rb +415 -0
  197. data/lib/roebe/base/next.rb +29 -0
  198. data/lib/roebe/base/opnn.rb +52 -0
  199. data/lib/roebe/base/prototype.rb +483 -0
  200. data/lib/roebe/base/reset.rb +50 -0
  201. data/lib/roebe/base/run.rb +17 -0
  202. data/lib/roebe/base/simp.rb +25 -0
  203. data/lib/roebe/base/support_for_beautiful_url.rb +35 -0
  204. data/lib/roebe/base/symlink.rb +51 -0
  205. data/lib/roebe/base/time.rb +165 -0
  206. data/lib/roebe/base/verbose_truth.rb +21 -0
  207. data/lib/roebe/base/write_what_into.rb +33 -0
  208. data/lib/roebe/browser/README.md +5 -0
  209. data/lib/roebe/browser/browser.rb +26 -0
  210. data/lib/roebe/browser/constants.rb +43 -0
  211. data/lib/roebe/browser/firefox.rb +51 -0
  212. data/lib/roebe/browser/menu.rb +103 -0
  213. data/lib/roebe/browser/misc.rb +367 -0
  214. data/lib/roebe/browser/output_url_then_open_in_browser.rb +168 -0
  215. data/lib/roebe/browser/palemoon.rb +59 -0
  216. data/lib/roebe/browser/reset.rb +50 -0
  217. data/lib/roebe/cat/class.rb +225 -0
  218. data/lib/roebe/cat/method.rb +14 -0
  219. data/lib/roebe/classes/add_irc_quote.rb +132 -0
  220. data/lib/roebe/classes/add_newline_after.rb +124 -0
  221. data/lib/roebe/classes/add_newline_after_n_characters.rb +65 -0
  222. data/lib/roebe/classes/add_this_user_to_the_sudoers_file.rb +67 -0
  223. data/lib/roebe/classes/add_user_lighty.rb +104 -0
  224. data/lib/roebe/classes/aggregate_all_files_together_from_this_directory.rb +86 -0
  225. data/lib/roebe/classes/aliases.rb +683 -0
  226. data/lib/roebe/classes/all_games.rb +61 -0
  227. data/lib/roebe/classes/all_my_gems.rb +101 -0
  228. data/lib/roebe/classes/alphabetical_sorter.rb +117 -0
  229. data/lib/roebe/classes/apache_configuration_maker.rb +234 -0
  230. data/lib/roebe/classes/append_this.rb +156 -0
  231. data/lib/roebe/classes/append_to_line.rb +141 -0
  232. data/lib/roebe/classes/ascii/README.md +2 -0
  233. data/lib/roebe/classes/ascii/fix_missing_numbers_for_ascii_paradise.rb +96 -0
  234. data/lib/roebe/classes/at.rb +340 -0
  235. data/lib/roebe/classes/audio_information/audio_information.rb +116 -0
  236. data/lib/roebe/classes/automounter.rb +181 -0
  237. data/lib/roebe/classes/available_classes.rb +219 -0
  238. data/lib/roebe/classes/backup_core_system.rb +223 -0
  239. data/lib/roebe/classes/basic_configure.rb +110 -0
  240. data/lib/roebe/classes/batch_generate_all_my_gems.rb +132 -0
  241. data/lib/roebe/classes/become_another_user.rb +86 -0
  242. data/lib/roebe/classes/bezirk.rb +91 -0
  243. data/lib/roebe/classes/birthday_notifications.rb +291 -0
  244. data/lib/roebe/classes/books/books.rb +452 -0
  245. data/lib/roebe/classes/books/menu.rb +171 -0
  246. data/lib/roebe/classes/burn_iso/burn_iso.rb +262 -0
  247. data/lib/roebe/classes/burn_iso/constants.rb +43 -0
  248. data/lib/roebe/classes/burn_iso/initialize.rb +33 -0
  249. data/lib/roebe/classes/caesar_cipher.rb +88 -0
  250. data/lib/roebe/classes/calendar.rb +360 -0
  251. data/lib/roebe/classes/calendar_maker.rb +61 -0
  252. data/lib/roebe/classes/celsius_to_fahrenheit.rb +195 -0
  253. data/lib/roebe/classes/check_for_bad_blocks.rb +67 -0
  254. data/lib/roebe/classes/check_yaml.rb +71 -0
  255. data/lib/roebe/classes/chmod_current_time.rb +71 -0
  256. data/lib/roebe/classes/clipboard.rb +221 -0
  257. data/lib/roebe/classes/clock.rb +118 -0
  258. data/lib/roebe/classes/colourize_numbers.rb +70 -0
  259. data/lib/roebe/classes/compare_these_two_directories.rb +101 -0
  260. data/lib/roebe/classes/compare_these_two_files.rb +167 -0
  261. data/lib/roebe/classes/compile_kernel.rb +114 -0
  262. data/lib/roebe/classes/config_generator.rb +204 -0
  263. data/lib/roebe/classes/conky.rb +114 -0
  264. data/lib/roebe/classes/conky_rcfile_generator.rb +61 -0
  265. data/lib/roebe/classes/convert_encoding_of_this_file.rb +215 -0
  266. data/lib/roebe/classes/convert_file_into_utf_encoding.rb +89 -0
  267. data/lib/roebe/classes/convert_this_cgi_file_into_a_sinatrafied_application.rb +145 -0
  268. data/lib/roebe/classes/copy_from_glibc.rb +134 -0
  269. data/lib/roebe/classes/copy_here.rb +76 -0
  270. data/lib/roebe/classes/copy_kernel_config.rb +59 -0
  271. data/lib/roebe/classes/copy_these_directories_to.rb +121 -0
  272. data/lib/roebe/classes/correct_gibberish.rb +89 -0
  273. data/lib/roebe/classes/covid_lethality.rb +243 -0
  274. data/lib/roebe/classes/create_asoundrc_file.rb +66 -0
  275. data/lib/roebe/classes/create_benchmark_file.rb +77 -0
  276. data/lib/roebe/classes/create_desktop_file.rb +236 -0
  277. data/lib/roebe/classes/create_docbook_sgml_dtd_catalog.rb +113 -0
  278. data/lib/roebe/classes/create_file_skeleton/constants.rb +70 -0
  279. data/lib/roebe/classes/create_file_skeleton/create_file_skeleton.rb +470 -0
  280. data/lib/roebe/classes/create_file_skeleton/generate_c_string.rb +31 -0
  281. data/lib/roebe/classes/create_file_skeleton/generate_cpp_string.rb +33 -0
  282. data/lib/roebe/classes/create_file_skeleton/generate_ruby_string.rb +124 -0
  283. data/lib/roebe/classes/create_file_skeleton/reset.rb +56 -0
  284. data/lib/roebe/classes/create_file_skeleton/run.rb +23 -0
  285. data/lib/roebe/classes/create_firefox_extension.rb +178 -0
  286. data/lib/roebe/classes/create_iso.rb +203 -0
  287. data/lib/roebe/classes/create_iso_for_games.rb +308 -0
  288. data/lib/roebe/classes/create_jar_archive.rb +58 -0
  289. data/lib/roebe/classes/create_my_directories.rb +208 -0
  290. data/lib/roebe/classes/create_ruby_directory_layout.rb +117 -0
  291. data/lib/roebe/classes/create_zip.rb +112 -0
  292. data/lib/roebe/classes/css_analyzer.rb +125 -0
  293. data/lib/roebe/classes/current_monitor_resolution.rb +107 -0
  294. data/lib/roebe/classes/custom_table/custom_table.rb +198 -0
  295. data/lib/roebe/classes/cut_after_colon.rb +80 -0
  296. data/lib/roebe/classes/daemonize.rb +131 -0
  297. data/lib/roebe/classes/date_sort.rb +149 -0
  298. data/lib/roebe/classes/day_calendar.rb +153 -0
  299. data/lib/roebe/classes/dbus.rb +127 -0
  300. data/lib/roebe/classes/delete_all_directories.rb +100 -0
  301. data/lib/roebe/classes/delete_empty_directories.rb +96 -0
  302. data/lib/roebe/classes/delete_empty_files.rb +146 -0
  303. data/lib/roebe/classes/dhcpcd.rb +139 -0
  304. data/lib/roebe/classes/differences_between_two_directories.rb +140 -0
  305. data/lib/roebe/classes/disable.rb +172 -0
  306. data/lib/roebe/classes/display_gcc_version.rb +135 -0
  307. data/lib/roebe/classes/do_a_google_search.rb +67 -0
  308. data/lib/roebe/classes/do_install.rb +337 -0
  309. data/lib/roebe/classes/done.rb +158 -0
  310. data/lib/roebe/classes/done_and_open.rb +183 -0
  311. data/lib/roebe/classes/doskey_generator.rb +198 -0
  312. data/lib/roebe/classes/downcase_directories.rb +83 -0
  313. data/lib/roebe/classes/downcase_extension.rb +131 -0
  314. data/lib/roebe/classes/download_from_this_url.rb +266 -0
  315. data/lib/roebe/classes/email.rb +648 -0
  316. data/lib/roebe/classes/enable.rb +60 -0
  317. data/lib/roebe/classes/enable_autologin.rb +371 -0
  318. data/lib/roebe/classes/english_to_german.rb +128 -0
  319. data/lib/roebe/classes/ethernet.rb +171 -0
  320. data/lib/roebe/classes/euclidian_distance.rb +148 -0
  321. data/lib/roebe/classes/extract_documentation.rb +191 -0
  322. data/lib/roebe/classes/extract_gem_file.rb +208 -0
  323. data/lib/roebe/classes/feet_to_centimetres.rb +106 -0
  324. data/lib/roebe/classes/fetch_random_line.rb +66 -0
  325. data/lib/roebe/classes/fetch_url.rb +77 -0
  326. data/lib/roebe/classes/file_parser.rb +126 -0
  327. data/lib/roebe/classes/file_renamer.rb +229 -0
  328. data/lib/roebe/classes/files_that_could_become_apps.rb +91 -0
  329. data/lib/roebe/classes/filter_apache_log.rb +90 -0
  330. data/lib/roebe/classes/find_all_files_encoded_in_iso.rb +95 -0
  331. data/lib/roebe/classes/find_all_files_with_a_question_mark.rb +148 -0
  332. data/lib/roebe/classes/find_duplicate_entries_in_alias_file.rb +160 -0
  333. data/lib/roebe/classes/find_empty_files.rb +80 -0
  334. data/lib/roebe/classes/find_expanded_alias.rb +259 -0
  335. data/lib/roebe/classes/find_out_version_of.rb +186 -0
  336. data/lib/roebe/classes/find_static_libraries.rb +213 -0
  337. data/lib/roebe/classes/fix_mcookie.rb +76 -0
  338. data/lib/roebe/classes/fix_timezone.rb +95 -0
  339. data/lib/roebe/classes/fluxbox/README.md +3 -0
  340. data/lib/roebe/classes/fluxbox/autogenerate_fluxbox_files.rb +20 -0
  341. data/lib/roebe/classes/fluxbox/generate_fluxbox_apps_file.rb +155 -0
  342. data/lib/roebe/classes/fluxbox/generate_fluxbox_keys_file.rb +110 -0
  343. data/lib/roebe/classes/fluxbox/install_fluxbox_style.rb +85 -0
  344. data/lib/roebe/classes/font_installer.rb +139 -0
  345. data/lib/roebe/classes/fotos_f/303/274r_ingrid.rb +50 -0
  346. data/lib/roebe/classes/fragment_maker.rb +141 -0
  347. data/lib/roebe/classes/general_overviewer.rb +258 -0
  348. data/lib/roebe/classes/generate_alsa_conf.rb +133 -0
  349. data/lib/roebe/classes/generate_etc_resolv_conf_file.rb +106 -0
  350. data/lib/roebe/classes/generate_fstab_file/generate_fstab_file.rb +255 -0
  351. data/lib/roebe/classes/generate_gemspec/constants.rb +58 -0
  352. data/lib/roebe/classes/generate_gemspec/generate_gemspec.rb +195 -0
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  2706. data/lib/roebe/www/vnc/vnc.sinatra +56 -0
  2707. data/lib/roebe/www/voice_recorders/voice_recorders.cgi +7 -0
  2708. data/lib/roebe/www/voice_recorders/voice_recorders.rb +48 -0
  2709. data/lib/roebe/www/voice_recorders/voice_recorders.sinatra +52 -0
  2710. data/lib/roebe/www/wahrscheinlichkeit/wahrscheinlichkeit.cgi +7 -0
  2711. data/lib/roebe/www/wahrscheinlichkeit/wahrscheinlichkeit.rb +270 -0
  2712. data/lib/roebe/www/wahrscheinlichkeit/wahrscheinlichkeit.sinatra +56 -0
  2713. data/lib/roebe/www/war_in_Ukraine_2022/war_in_Ukraine_2022.cgi +7 -0
  2714. data/lib/roebe/www/war_in_Ukraine_2022/war_in_Ukraine_2022.rb +155 -0
  2715. data/lib/roebe/www/war_in_Ukraine_2022/war_in_Ukraine_2022.sinatra +56 -0
  2716. data/lib/roebe/www/waschmaschinen/waschmaschinen.cgi +7 -0
  2717. data/lib/roebe/www/waschmaschinen/waschmaschinen.rb +145 -0
  2718. data/lib/roebe/www/waschmaschinen/waschmaschinen.sinatra +52 -0
  2719. data/lib/roebe/www/webserving/webserving.cgi +7 -0
  2720. data/lib/roebe/www/webserving/webserving.rb +905 -0
  2721. data/lib/roebe/www/webserving/webserving.sinatra +52 -0
  2722. data/lib/roebe/www/weechat/weechat.cgi +7 -0
  2723. data/lib/roebe/www/weechat/weechat.rb +166 -0
  2724. data/lib/roebe/www/weechat/weechat.sinatra +52 -0
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  2726. data/lib/roebe/www/wein/wein.rb +16 -0
  2727. data/lib/roebe/www/wein/wein.sinatra +56 -0
  2728. data/lib/roebe/www/wget/wgetrc +124 -0
  2729. data/lib/roebe/www/why_linux/why_linux.cgi +7 -0
  2730. data/lib/roebe/www/why_linux/why_linux.rb +301 -0
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  2733. data/lib/roebe/www/wikis/wikis.rb +18 -0
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  2736. data/lib/roebe/www/wine/wine.rb +323 -0
  2737. data/lib/roebe/www/wine/wine.sinatra +52 -0
  2738. data/lib/roebe/www/wine/wine_config +69 -0
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  2772. data/lib/roebe/www/zitieren/example.md +10 -0
  2773. data/lib/roebe/www/zitieren/wie_zitiert_man_in_der_Wissenschaft_richtig.md +261 -0
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  2798. data/lib/roebe/yaml/escape_codes/escape_codes.yml +12 -0
  2799. data/lib/roebe/yaml/famous_bboys/famous_bboys.yml +14 -0
  2800. data/lib/roebe/yaml/file_information.yml +34 -0
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  2802. data/lib/roebe/yaml/forbidden_IPs.yml +2 -0
  2803. data/lib/roebe/yaml/fstab/fstab.yml +122 -0
  2804. data/lib/roebe/yaml/funstuff/am/303/274sante_deutsche_w/303/266rter.yml +2 -0
  2805. data/lib/roebe/yaml/gnome/gnome.yml +8 -0
  2806. data/lib/roebe/yaml/holidays/holidays.yml +24 -0
  2807. data/lib/roebe/yaml/http_status_codes/http_status_codes.yml +52 -0
  2808. data/lib/roebe/yaml/individual_environment_variables/cflags.yml +59 -0
  2809. data/lib/roebe/yaml/individual_environment_variables/lang.yml +75 -0
  2810. data/lib/roebe/yaml/individual_environment_variables/ldflags.yml +2 -0
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  2812. data/lib/roebe/yaml/ip_suffix/ip_suffix.yml +22 -0
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  2849. data/lib/roebe/yaml/test/README.md +4 -0
  2850. data/lib/roebe/yaml/test/umlaute.yml +2 -0
  2851. data/lib/roebe/yaml/the_beginning_of_linux/the_beginning_of_linux.yml +29 -0
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  2889. data/test/testing_twentyfour_hours_notation.rb +37 -0
  2890. data/test/testing_zenity.rb +26 -0
  2891. metadata +3023 -0
@@ -0,0 +1,1009 @@
1
+ english('Microbiology') {
2
+ autoextend
3
+ ruby_favicon
4
+ default_template '
5
+
6
+ a,
7
+ a:link { text-decoration: none; color: steelblue; font-weight: bold;}
8
+ a:hover { text-decoration: underline; color: royalblue; font-weight: bold;}
9
+
10
+ p,
11
+ p.default {
12
+ margin: 0.2em;
13
+ padding: 0.3em;
14
+ }
15
+ div.default {
16
+ margin: 8px;
17
+ padding: 12px;
18
+ }
19
+ '
20
+ body_css_class 'mar0px s2px padt2px VERDANAs'
21
+ body_css_style 'background-color: #d3d2d1;'
22
+ font_size '1.2em'
23
+
24
+ doc('mar0px pad0px s1em') {
25
+ h1 dot(105, 'marr8px')+
26
+ 'Microbiology',
27
+ 'mart1px marb0_5em'
28
+ # ========================================================================= #
29
+ # === Bacterias
30
+ # ========================================================================= #
31
+ header 'Bacteria','martb8px'
32
+ p_default('ind0 FW4'){
33
+ e 'Here is a textbook - everything about microbes.'
34
+ br
35
+ a 'http://textbookofbacteriology.net/',
36
+ content: '→ All about Microbes',
37
+ css_class: 'BOLD mars1em'
38
+ }
39
+ # ========================================================================= #
40
+ # === Phantom microbes
41
+ # ========================================================================= #
42
+ header 'Phantom microbes','martb8px'
43
+ p_default {
44
+ e "The so-called <b>'phantom microbes'</b> can not be cultured.
45
+ We know about them because we can <b>use modern genomic techniques
46
+ to expose their existence</b>."
47
+ }
48
+ # ========================================================================= #
49
+ # === Streptococcus pyogenes
50
+ # ========================================================================= #
51
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/microbiology/microbiology.cgi#streptococcus_pyogenes
52
+ # ========================================================================= #
53
+ header 'Streptococcus pyogenes','martb8px'
54
+ p_default(id: 'streptococcus_pyogenes') {
55
+ e 'The natural environment - or, at the least, a popular environment -
56
+ for <i>Streptococcus pyogenes</i> is <b>the human oral cavity</b>. Due
57
+ to this environment, S. pyogenes does not need to synthesize glutamtic
58
+ acid and alanine. It has thus <b>lost the genes</b> whose protein
59
+ products synthesize tehse aminoacids.'
60
+ }
61
+ # ========================================================================= #
62
+ # === Spirochete
63
+ # ========================================================================= #
64
+ header 'Spirochete','martb8px'
65
+ p('ind0 FW4'){
66
+ e 'Spirochete have a fairly interesting shape. The following image shows
67
+ this:'
68
+ br
69
+ dimg 'science/microbiology/Spirochete.jpg',
70
+ 'bblack2 mars2em'
71
+ }
72
+ # ========================================================================= #
73
+ # === Die Gramfärbung
74
+ # ========================================================================= #
75
+ header 'Gramfärbung - Schritte:','martb8px'
76
+ div_default('martb8px') {
77
+ p_default {
78
+ e '- Hitzefixierung'
79
+ e '- Kristallviolet (Bakterien werden blau)'
80
+ ee '- Safranin-Gegenfärbung'
81
+ }
82
+ }
83
+ # ========================================================================= #
84
+ # === Symbionts
85
+ # ========================================================================= #
86
+ header 'Symbionts','martb8px'
87
+ div_default('martb5px') {
88
+ e 'A symbiont is an organism that lives in intimate association with
89
+ (at the least) a second organism.'
90
+ }
91
+ # ========================================================================= #
92
+ # === Quorum sensing in bacteria
93
+ # ========================================================================= #
94
+ header 'Quorum sensing in bacteria','martb8px'
95
+ div_default('martb5px') {
96
+ e '<b>Quorum sensing</b> allows bacteria to <b>coordinate</b> their
97
+ behavior, including their motility, antibiotic production, spore
98
+ formation and sexual conjugation.'
99
+ }
100
+ # ========================================================================= #
101
+ # === E. coli TEMP cell wall
102
+ # ========================================================================= #
103
+ header 'E. coli TEM cell wall picture','martb8px'
104
+ div_default('martb5px') {
105
+ dimg 'science/microbiology/Escherichia_coli_TEM_cell_wall.jpg',
106
+ 'bblack2 mar1em'
107
+ br
108
+ e 'The ATP operon in E. coli is organized in the following manner:'
109
+ br
110
+ dimg 'science/microbiology/ATP_OPERON_ECOLI.png',
111
+ 'bblack2 mar1em'
112
+ }
113
+ # ========================================================================= #
114
+ # === Bacteria and disease
115
+ # ========================================================================= #
116
+ header 'Bacteria and disease','martb8px'
117
+ div_default('martb5px') {
118
+ e 'The causative agent of syphilis is <i>Treponema pallidum</i>,
119
+ a <b>spirochaete</b>. The drug <b>Salvarsan</b> was historically
120
+ used to combat this microorganism.'
121
+ }
122
+ # ========================================================================= #
123
+ # === Flagella in Bacteria
124
+ # ========================================================================= #
125
+ div(id: 'flagella') {
126
+ header 'Flagella in Bacteria'
127
+ boldbr 'Peritrichous flagella:'
128
+ dimg 'science/microbiology/peritrichous_flagella.png',
129
+ 'bblack2 mar1em mars3em'
130
+ br
131
+ boldbr 'Lophotrichous flagella:'
132
+ dimg 'science/microbiology/lophotrichous_flagella.png',
133
+ 'bblack2 mar1em mars3em'
134
+ br
135
+ boldbr 'Polar flagella:'
136
+ dimg 'science/microbiology/polar_flagella.png',
137
+ 'bblack2 mar1em mars3em'
138
+ br
139
+ e 'The electron microscopy image in gram-negative bacteria
140
+ looks like this:'
141
+ br
142
+ dimg 'science/microbiology/flagellum_in_gram_negative_bacteria.png',
143
+ 'bblack3 mars3em'
144
+ }
145
+ # ========================================================================= #
146
+ # === Bakterien auf den Händen.
147
+ #
148
+ # 04.11.2008
149
+ #
150
+ # URL: https://science.orf.at/science/news/153184
151
+ # ========================================================================= #
152
+ div {
153
+ datum '04.11.2008','BG_Black pad0_5em gold'
154
+ h2 'Bakterien auf den Händen'
155
+ e 'Frauen haben mehr Bakterien an den Händen als Männer. Der Grund
156
+ liegt sehr wahrscheinlich darin begründet, dass der saure Schweiß
157
+ der Männer für diesen Unterschied verantwortlich ist.'
158
+ br
159
+ e 'An unseren Händen tummeln sich pro Quadratzentimeter mehr als zehn
160
+ Millionen Bakterien.'
161
+ br
162
+ e 'Im <b>PNAS</b> (doi: 10.1073/pnas.0807920105)
163
+ "<i>The influence of sex, handedness, and washing on the
164
+ diversity of hand surface bacteria</i>" wird berichtet das die
165
+ Handinnenflächen quasi der "<i>tropische Regenwald der Epidermis</i>"
166
+ sind: Satte 4.700 verschiedene Bakterienarten fanden sich auf
167
+ den 102 analysierten Händen.'
168
+ br
169
+ e 'Interessanterweise dürfte das <b>bakterielle Profil</b> eine
170
+ recht individuelle Angelegenheit sein, denn davon kamen nur fünf
171
+ auf allen Händen vor.'
172
+ br
173
+ e 'Selbst zwischen rechter und linker Hand derselben Testperson
174
+ gab es beträchtliche Unterschiede. Die Übereinstimmung betrug,
175
+ nach Arten gerechnet, lediglich 17 Prozent - was nicht viel
176
+ mehr ist als die Deckung zweier zufällig ausgewählter Hände,
177
+ nämlich 13 Prozent.'
178
+ br
179
+ e 'Frauen besitzen <b>mehr Bakterienarten</b> auf ihren
180
+ Händen als Männer.'
181
+ br
182
+ e 'Die Unterschiede im Artenspektrum könnte man mit dem pH-Wert
183
+ des Schweißes erklären.'
184
+ br
185
+ e 'Aus Studien an anderen Ökosystemen weiß man, dass ein
186
+ niedriger pH-Wert der Bakterienvielfalt eher abträglich ist.'
187
+ br
188
+ e 'Händewaschen beeinflusst der Studie zufolge die bakterielle
189
+ Vielfalt kaum.'
190
+ }
191
+ # ========================================================================= #
192
+ # === Transcription in bacteria
193
+ # ========================================================================= #
194
+ h2 'Transcription in <i>bacteria</i>'
195
+ div_default {
196
+ e 'The σ-factor (sigma-factor) is important to detect
197
+ promoters. This is also called discrimination, e. g.
198
+ to discriminate between different DNA sequences. After
199
+ initiation of transcription the σ-factor dissociates
200
+ from the complex assembled around the RNA polymerase
201
+ again.'
202
+ }
203
+ # ========================================================================= #
204
+ # === Kanamycin tag
205
+ # ========================================================================= #
206
+ h2 'Kanamycin <span class="subtitle">Antibiotikum</span>'
207
+ div(id: 'kanamycin') {
208
+ e '<b>Kanamycin</b> ist ein <b class="ud">Aminoglycosid-Antibiotikum</b>
209
+ aus <b>Streptomyceten</b> (Streptomyces kanamyceticus).'
210
+ br
211
+ e 'Es ist ein basisches, stark polares Oligosaccharid, farblos, gut
212
+ wasserlöslich und im pH-Bereich von 2,2 - 10,0 lösungsstabil.'
213
+ br
214
+ e 'Kanamycin durchdringt die bakteriellen Zellmembranen durch passive
215
+ Diffusion oder durch sauerstoffabhängigen, aktiven Transport. Es lagert
216
+ sich an die 30S-Untereinheit membranassoziierter bakterieller Ribosomen
217
+ an und hemmt damit die (bakterielle) Proteinsynthese.'
218
+ br
219
+ e 'In der <b>Humanmedizin</b> wird es als <b>Sulfatsalz</b> in Form
220
+ von Augentropfen/salben eingesetzt. Handelsübliches Kanamycin ist ein
221
+ Gemisch aus den Kanamycinen A, B und C.'
222
+ br
223
+ e 'Eine typische Infektion des <b>Lidrandes</b> ist beispielsweise
224
+ das Gerstenkorn. Dabei handelt es sich um eine akute Infektion der
225
+ Schweißdrüsen am Rand des Auges oder an der Talgdrüse im Lid
226
+ mit eitererregenden Bakterien (<b>Staphylokokken</b>).'
227
+ }
228
+ # ========================================================================= #
229
+ # === Phosphotransferase
230
+ # ========================================================================= #
231
+ div(id: 'phosphotransferase') {
232
+ h4 'Phosphotransferase'
233
+ dimg 'science/chemistry/PHOSPHOTRANSFERASESYSTEM.jpg',
234
+ 'bblack3'
235
+ }
236
+ # ========================================================================= #
237
+ # === The trp-operon (trp tag)
238
+ # ========================================================================= #
239
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/microbiology/microbiology.cgi#trp
240
+ # ========================================================================= #
241
+ h2 'The trp-operon in bacteria'
242
+ div_default(id: 'trp') {
243
+ e "Let's look at the <b>trp operon</b> in <i>E. coli</i> next."
244
+ br
245
+ e 'This operon codes for the necessary biosynthetic enzymes that
246
+ will ultimately synthesize the amino acid tryptophan.'
247
+ br
248
+ e 'The trp operon is turned on - that is, expressed - when tryptophan
249
+ levels are low. Conversely it is turned off - that is, repressed -
250
+ when the tryptophan levels are high.'
251
+ br
252
+ e 'The trp operon is regulated by the <b>trp repressor</b>.
253
+ This repressor, when bound to tryptophan, will block
254
+ the expression of the operon.'
255
+ br
256
+ e 'If tryptophan is available in the environment then <i>E. coli</i>
257
+ will take it up and use it to build proteins. Under this condition
258
+ tryptophan will not be synthesized by <i>E. coli</i>.'
259
+ br
260
+ e 'The <b>trp operon</b> in <i>E. coli</i> consists of <b>five
261
+ structural genes</b>, called
262
+ <b>trpE</b> (encodes enzyme Anthranilate synthase I),
263
+ <b>trpD</b> (encodes the enzyme Anthranilate synthase II),
264
+ <b>trpC</b>, <b>trpB</b>, and <b>trpA</b>. TrpA and TrpB
265
+ are the two subunits of the <b>tryptophan synthetase</b>.'
266
+ br
267
+ e 'The operon has a so-called <b>leader sequence</b> upstream
268
+ of the coding region of the trpE structural gene. This leader
269
+ sequence encodes a 14 amino acid leader peptide containing
270
+ two tryptophan residues one after the other.'
271
+ br
272
+ e 'The repressor is encoded by gene <b>trpR</b>.'
273
+ br
274
+ e 'The trp operator region partly overlaps the trp
275
+ promoter.'
276
+ br
277
+ e 'If tryptophan is present then the trpR protein will bind
278
+ to the operator, which will block transcription of the trp
279
+ operon by the RNA polymerase.'
280
+ br
281
+ e '<b>Tryptophan biosynthesis</b> is additionally regulated by
282
+ a process called <b>attenuation</b> - a mechanism based on
283
+ coupling of transcription and translation. This is a second
284
+ mechanism of negative feedback in the trp operon, interestingly
285
+ enough. This secondary regulation, via attenuation, responds
286
+ to the concentration of charged tRNAtrp. Rather than blocking
287
+ initiation of transcription, <b>attenuation</b> prevents
288
+ <b>completion</b> of transcription.'
289
+ br
290
+ e 'Thus, the trpR repressor decreases gene expression by
291
+ altering the initiation of transcription, whereas attenuation
292
+ does so by altering the process of transcription that is
293
+ already in progress. In this role, tryptophan is said to be
294
+ a <b>co-repressor</b>. It is called <b>negative control</b>,
295
+ because <b>the bound repressor prevents transcription</b>.'
296
+ br
297
+ e 'While the TrpR repressor decreases transcription by a
298
+ factor of 70, attenuation can further decrease it by a
299
+ factor of 10, thus allowing accumulated repression of
300
+ about <b>700-fold</b>.'
301
+ br
302
+ e 'Attenuation is made possible by the fact that in prokaryotes
303
+ the ribosomes begin translating the mRNA while the RNA polymerase
304
+ is still transcribing the DNA sequence. This allows the process of
305
+ translation to affect transcription of the operon directly. The
306
+ process of attenuation involves the presence of a stop signal
307
+ that indicates premature termination.'
308
+ br
309
+ e "When levels of tryptophan are high, attenuation causes
310
+ RNA polymerase to stop prematurely when it is transcribing
311
+ the trp operon. Only a short mRNA is made, not encoding any
312
+ of the tryptophan biosynthesis enzymes. Attenuation works
313
+ through a mechanism that depends on coupling (the
314
+ translation of an mRNA that is still in the process of
315
+ being transcribed)."
316
+ br
317
+ e 'At the beginning of the transcribed genes of the trp
318
+ operon is a sequence of at least 130 nucleotides termed
319
+ the leader transcript: <b>trpL</b>,
320
+ see <a href="https://www.ncbi.nlm.nih.gov/protein/NP_415781.1?report=fasta">
321
+ NP_415781.1</a>.'
322
+ br
323
+ e 'Lee and Yanofsky found that the attenuation efficiency is
324
+ correlated with the stability of a secondary structure embedded
325
+ in trpL. Hairpins will form that give rise to a
326
+ terminator structure, as elucidated by Oxender et al. in 1979.'
327
+ br
328
+ e 'This transcript includes four short sequences, designate
329
+ 1, 2, 3 and 4.'
330
+ br
331
+ e 'These sequences are partially complementary to the next one.'
332
+ br
333
+ e 'Thus, three distinct hairpins, as secondary structures,
334
+ can form.'
335
+ br
336
+ e 'These are:'
337
+ br
338
+ cmd '1-2'
339
+ cmd '2-3 # formed when there is a lack of tryptophan'
340
+ cmd '3-4 # formed when tryptophan is in abundance; this
341
+ is then called the <b>attenuator</b>'
342
+ br
343
+ e 'From the above, it can be logically inferred that region
344
+ 3 is complementary to both region 2 and region 4.'
345
+ br
346
+ embed_remote_image 'https://textimgs.s3.amazonaws.com/boundless-microbiology/trp-operon-attenuation.svg#fixme',
347
+ 'mar1em bblack3'
348
+ br
349
+ e 'This is all made possible by RNA-to-RNA base pairings -
350
+ thus <b>hairpin loops</b>.'
351
+ br
352
+ e 'Hybridization of sequences 1 and 2 to form the 1-2 structure
353
+ is rare because the RNA polymerase waits for a ribosome to
354
+ attach before continuing transcription past sequence 1.
355
+ If, however, 1-2 hairpin were to form it would prevent the
356
+ formation of the 2-3 structure (but not 3-4).'
357
+ br
358
+ e 'The formation of a hairpin loop between sequences 2-3 prevents
359
+ the formation of hairpin loops between both 1-2 and 3-4.'
360
+ br
361
+ e 'The 3-4 structure is a transcription termination sequence
362
+ (abundant in G/C and immediately followed by several uracil
363
+ residues). Once it forms RNA polymerase will disassociate
364
+ from the DNA and transcription of the structural genes of
365
+ the operon can not occur.'
366
+ br
367
+ e 'Part of the leader transcript codes for a short polypeptide
368
+ of 14 amino acids, termed the leader peptide. This peptide
369
+ contains two adjacent tryptophan residues, which is unusual,
370
+ since tryptophan is a fairly uncommon amino acid (about one
371
+ in a hundred residues in a typical E. coli protein is
372
+ tryptophan).'
373
+ br
374
+ e 'The strand 1 in trpL encompasses the region encoding the
375
+ trailing residues of the leader peptide: Trp, Trp, Arg, Thr,
376
+ Ser.'
377
+ br
378
+ dimg 'science/biology/operons/the_trp_operon.png',
379
+ 'bblack3 mar1em mars3em BG_White'
380
+ }
381
+ # ========================================================================= #
382
+ # === The bacterial SRP - an example for a co-translational process
383
+ # ========================================================================= #
384
+ h2 'The bacterial SRP - an example for a co-translational process'
385
+ div_default {
386
+ e 'The <b>SRP</b> is the signal-recognition particle, a
387
+ <b>ribonucleoprotein</b>. It is important for the proper localization
388
+ of newly synthesized proteins and can be found in the <b>cytosol</b>
389
+ of a cell. It can recognize and bind to the signal peptide of such
390
+ newly synthesized proteins.'
391
+ br
392
+ e 'The SRP will deliver the complex of ribosome and mRNA towards the
393
+ rough endoplasmic reticulum (RER) and will then bind to the SRP
394
+ receptor there.'
395
+ br
396
+ e 'In bacteria, about 30% of the newly synthesized proteins may be
397
+ relocated towards the bacterial plasma membrane.'
398
+ br
399
+ e 'The SRP is ultimately a <b>protein targeting machine</b>.
400
+ Its receptor is membrane-bound. The SRP exists in both
401
+ eukaryotes and prokaryotes - at the least as a homologue.'
402
+ br
403
+ e 'The typical composition of the SRP is of the following
404
+ six polypeptides, named after their molecular weight:'
405
+ br
406
+ cmd ' SRP9, SRP14, SRP19, SRP54, SRP68 and SRP72'
407
+ br
408
+ e 'In addition to that the 7SL-RNA can be seen here, also
409
+ known as SRP-RNA. The 7SL RNA is also a precursor of the
410
+ <b>Alu elements</b> in the human genome.'
411
+ br
412
+ e 'In Eukaryotes, SRP-mediated protein targeting is a
413
+ cotranslational process that begins when a nascent
414
+ polypeptide destined for the ER or plasma membrane
415
+ emerges from the ribosome.'
416
+ br
417
+ e 'Important here is the N-terminal signal sequence on
418
+ the nascent polypeptide. This is the signal that
419
+ allows the cargo to engage the SRP. Through interaction
420
+ with the SRP receptor it is then delivered to the
421
+ vicinity of the <b>Sec61p</b> - or <b>SecYEG</b> in
422
+ prokaryotes translocon at the target membrane.'
423
+ br
424
+ e 'Interestingly, the bacterial SRP, though highly simplified
425
+ compared to those in eukaryotes, can replace their
426
+ mammalian homologues to mediate efficient targeting
427
+ of mammalian proteins to the ER. The functional core of
428
+ the SRP is thus sufficient for protein targeting and it
429
+ can be represented by the bacterial machinery even in
430
+ eukaryotic cells. The bacterial FtsY can be found at
431
+ the plasma membrane.'
432
+ br
433
+ e 'The bacterial SRP contains the universally conserved
434
+ <b>SRP54 protein</b> - called Ffh in bacteria - bound
435
+ to the 4.5S SRP RNA. Ffh has two primary domains:'
436
+ br
437
+ e '- a methionine-rich M-domain. This domain recognizes the
438
+ signal sequence and binds to the SRP RNA.'
439
+ e '- a special GTPase (the NG-domain). This one interacts
440
+ with the NG-domain in the SR.'
441
+ br
442
+ e 'The <b>cotranslational SRP pathway</b> minimizes the
443
+ aggregation or misfolding of nascent proteins before they
444
+ arrive at their cellular destination.'
445
+ br
446
+ e 'Links:'
447
+ br
448
+ abr 'https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3805129/',
449
+ content: 'Signal Recognition Particle: An essential protein targeting machine (Feb 2013)',
450
+ css_class: 'BOLD mars1em'
451
+ }
452
+ # ========================================================================= #
453
+ # === Infektionen
454
+ # ========================================================================= #
455
+ h2 'Infektionen'
456
+ p_default {
457
+ e 'Der häufigste natürliche Verlauf einer Infektionskrankheit ist die
458
+ akute, ausheilende Infektion.'
459
+ }
460
+ # ========================================================================= #
461
+ # === Topoisomerases in Bacteria
462
+ # ========================================================================= #
463
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/microbiology/microbiology.cgi#topoisomerases
464
+ # ========================================================================= #
465
+ h2 'Topoisomerases in Bacteria'
466
+ p_default(id: 'topoisomerases') {
467
+ e '<b>Topoisomerases</b> are <b>enzymes</b> that <b>catalyze changes
468
+ in the topological state of DNA</b> - in other words, they can
469
+ <b>alter DNA topology</b> by interconverting relaxed and supercoiled
470
+ forms of DNA into one another.'
471
+ br
472
+ e 'Topological issues in DNA arise due to the intertwined nature
473
+ of its double-helical structure, such as <b>during DNA replication</b>
474
+ and transcription. Without the actions of Topoisomerases,
475
+ RNA and DNA polymerases could not progress along the DNA.'
476
+ br
477
+ e 'The processes of DNA supercoiling and transcription are
478
+ interdependent because the movement of a transcription
479
+ elongation complex simultaneously induces under- and overwinding
480
+ of the DNA duplex.'
481
+ br
482
+ e 'The first DNA topoisomerase was discovered in bacteria
483
+ by James Wang in the year <b>1971</b>. It is now called
484
+ Escherichia coli (E. coli) topoisomerase I (topo I).'
485
+ br
486
+ e 'DNA topoisomerases are classified based on whether they
487
+ create a single- or double-stranded break in the DNA
488
+ phosphodiester backbone. class I uses single-stranded
489
+ breaks; class II uses double-stranded breaks.'
490
+ br
491
+ boldbr 'Links:'
492
+ br
493
+ abr_self 'https://academic.oup.com/nar/article/40/20/10432/2414715',
494
+ css_class: 'mars1em BOLD' # 2012
495
+ abr_self 'https://bmcmolcellbiol.biomedcentral.com/articles/10.1186/s12860-019-0211-6',
496
+ css_class: 'mars1em BOLD' # 2019
497
+ }
498
+ # ========================================================================= #
499
+ # === Disinfectants
500
+ # ========================================================================= #
501
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/microbiology/microbiology.cgi#disinfectants
502
+ # ========================================================================= #
503
+ h2 'Disinfectants',
504
+ id: 'disinfectants'
505
+ div_default_english {
506
+ e '<b>Alcohol</b> can be used as a disinfectant against microorganisms.
507
+ Interestingly enough, the concentration for this is more effective
508
+ below 100%; typically a concentration of 70% is used. This is because
509
+ the denaturation of proteins - but also membranes - proceeds more
510
+ effectively in the presence of water. For similar reasons, alcohol
511
+ will be more damaging to microbial membranes if there is water
512
+ available.'
513
+ br
514
+ e '<b>Moist heat</b> is also <b>more effective</b> than <b>dry heat</b>
515
+ for the same reasons.'
516
+ }
517
+ # ========================================================================= #
518
+ # === Aquaporins
519
+ # ========================================================================= #
520
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/microbiology/microbiology.cgi#aquaporins
521
+ # ========================================================================= #
522
+ h2_id 'Aquaporins'
523
+ div_default_english {
524
+ e 'Aquaporins can increase the rate of diffusion of water and
525
+ glycerol across cell membranes.'
526
+ br
527
+ e 'Not all bacteria contain aquaporins - for instance,
528
+ <b>aqpZ</b> was found in all four <b>Escherichia coli</b>
529
+ strains for which whole genome sequences were available
530
+ (in 2002), as well as in <i>Shigella flexneri</i>. It
531
+ does, however had, not occur in the closely related
532
+ bacteria such as <i>Salmonella enterica serovar Typhimurium</i>
533
+ or in <i>Yersinia pestis</i>.'
534
+ br
535
+ abr_self 'https://journals.asm.org/doi/10.1128/JB.184.15.4304-4307.2002' # 01.08.2002
536
+ }
537
+ # ========================================================================= #
538
+ # === The two-component regulatory system in prokaryotes
539
+ # ========================================================================= #
540
+ # http://localhost/programming/ruby/src/roebe/lib/roebe/www/microbiology/microbiology.cgi#the_two-component_regulatory_system_in_prokaryotes
541
+ # ========================================================================= #
542
+ h2_id 'The two-component regulatory system in prokaryotes'
543
+ div_default_english {
544
+ e '<i>Bacteria</i> must be able to sense their environment.'
545
+ br
546
+ e 'One sensor-system widespread among them is the
547
+ <b>two-component regulatory system</b>.'
548
+ br
549
+ e 'Here, the so-called <b>sensor kinase</b> (a <b>histidine kinase</b>)
550
+ will auto-phosphorylate itself, at a histidine.'
551
+ br
552
+ e 'The activity of the response regulator in the <b>two-component
553
+ systems</b> depends on the level of phosphorylation. The phosphate
554
+ group is passed to the response regulator, which typically has a
555
+ slow phosphatase activity to remove that phosphate group again.
556
+ Alternatively another protein will remove that phosphate group
557
+ and thus reset the system to its default state.'
558
+ br
559
+ e '<i>E. coli</i> has about 50 different two-component systems. One of
560
+ these is the OmpC / OmpF systems (two porines). They will regulate
561
+ the osmotic pressure in <i>E. coli</i>.'
562
+ br
563
+ abr_self 'https://en.wikipedia.org/wiki/EnvZ/OmpR_two-component_system'
564
+ }
565
+ # ========================================================================= #
566
+ # === Cell division in bacteria
567
+ # ========================================================================= #
568
+ h2_id 'Cell division in bacteria'
569
+ div_default {
570
+ e '<b>FtsA</b> and <b>ZipA</b> anchor the Z-ring into the cytoplasmic
571
+ membrane.'
572
+ }
573
+ # ========================================================================= #
574
+ # === Aufbau und Funktion des Zwei-Komponenten System.
575
+ # ========================================================================= #
576
+ h2_id 'Aufbau und Funktion des Zwei-Komponenten-System BvgSA'
577
+ div_default {
578
+ lembre '- membranständige Histidinkinase BvgS'
579
+ lembre '- zytoplasmatischer Transkriptionsfaktor BvgA'
580
+ br
581
+ e '<b>BvgS</b> ist das Sensorprotein, das Umweltreize mittels einer
582
+ Serie von Phosphorylierungsreaktionen, die letztlich zur Aktivierung
583
+ von BvgA führen, in ein zelluläres Signal umwandelt. BvgA bindet
584
+ daraufhin an die Promotoren der Virulenzgene und induziert deren
585
+ Transkription.'
586
+ br
587
+ e 'BvgAS gehört zur kleinen Gruppe der unorthodoxen Systeme, die
588
+ eine komplexere Domänenstruktur besitzen als die typischen
589
+ Zwei-Komponenten-Systeme:'
590
+ br
591
+ e 'So besitzt das BvgS Protein C-terminal zusätzliche
592
+ Domänen, die in klassischen Sensorproteinen nicht vorkommen.
593
+ Bei diesen unorthodoxen Systemen erfolgt ein über mehrere Domänen
594
+ ablaufender zwischen Histidin- und Aspartatresten alternierender
595
+ Phosphorelay.'
596
+ br
597
+ e 'Durch Mutations- und Komplementationsanalysen kann gezeigt
598
+ werden, daß die zusätzlichen BvgS Domänen für die Funktion von
599
+ BvgS essentiell sind und der Phosphorelay obligat ist. Durch den
600
+ Vergleich mit dem strukturell ähnlich gebauten EvgAS
601
+ Zwei-Komponenten-Systems von E. coli kann auch die der
602
+ C-terminalen BvgS Domäne bei der Spezifität der Signalübertragung
603
+ auf das Regulatorprotein BvgA belegt werden.'
604
+ br
605
+ e 'Die Expression dieser Faktoren wird durch Umweltfaktoren wie
606
+ zum Beispiel die Temperatur gesteuert.'
607
+ }
608
+ # ========================================================================= #
609
+ # === Slogans tag
610
+ # ========================================================================= #
611
+ h1 'Slogans'
612
+ p('mars2em') {
613
+ e 'The science of microbiology is all about <b>microorganisms</b>.'
614
+ br
615
+ e 'Microbiology is the study of the dominant form of life on Earth.'
616
+ br
617
+ e 'Microscopy is foundational to microbiology.'
618
+ br
619
+ e 'In microbiology the word <b>growth</b> refer to the increase in
620
+ cell number as a result of cell division.'
621
+ br
622
+ e 'The ability to grow microorganisms rapidly under controlled
623
+ conditions makes them highly useful for experiments that
624
+ probe the fundamental processes of life.'
625
+ br
626
+ e 'In nature, microbial cells typically live in groups called
627
+ microbial communities.'
628
+ br
629
+ e 'Microorganisms have the ability to sense and respond to
630
+ changes in their local environment.'
631
+ br
632
+ e "Cyanobacteria began the slow process of oxygenating Earth's
633
+ atmosphere."
634
+ br
635
+ e 'There are an estimated 2 * 10³⁰ microbial cells on Earth.'
636
+ br
637
+ e "The total amount of carbon present in all microbial cells
638
+ is a significant fraction of Earth’s biomass."
639
+ br
640
+ e 'Microbes represent <b>a major fraction of the total DNA in
641
+ the biosphere</b> - about <b>31%</b>.'
642
+ br
643
+ e 'Extremophiles and their properties define the physiochemical
644
+ limits to life as we know it.'
645
+ br
646
+ e 'Most microorganisms are not harmful to humans but instead are
647
+ beneficial. In many cases they are even essential to human
648
+ welfare and the functioning of the planet.'
649
+ br
650
+ e 'Microbes are intimately associated with the foods we eat.'
651
+ br
652
+ e 'Fermentation products affect the flavor and taste of foods.'
653
+ br
654
+ e 'Biofilms are of great importance in medicine, as biofilms
655
+ that form on implanted medical devices can cause infections
656
+ that are extremely difficult to treat.'
657
+ br
658
+ e 'Microbial diversity in the human colon is quite high.'
659
+ br
660
+ e 'Microorganisms in wastewater treatment are essential to
661
+ sanitation and human health. Waterborne diseases such as
662
+ cholera or typhoid can proliferate in the absence of proper
663
+ wastewater treatment, which reinforces the notion that this
664
+ is vital to human health.'
665
+ br
666
+ e 'The goal of bioremediation is to accelerate the cleanup
667
+ process and degrade the pollutants in the environment.'
668
+ br
669
+ e 'Microscopes provide an essential portal though which
670
+ microbiologists can gaze into the world of microbes.'
671
+ br
672
+ e 'Although staining is widely used in light microscopy,
673
+ staining often kills cells and can distort their
674
+ features.'
675
+ br
676
+ e 'Dark-field microscopy is a particularly good way to
677
+ observe microbial motility, as bundles of flagella are
678
+ often resolvable with this technique.'
679
+ br
680
+ e 'Fluorescence microscopy using DAPI is widely used in
681
+ clinical diagnostic microbiology. It is also used in
682
+ microbial ecology for enumerating bacteria in a natural
683
+ environment or in a cell suspension.'
684
+ br
685
+ e 'Sterile means "without the presence of living organisms".
686
+ Aseptic techniques are essential for the isolation and
687
+ maintenance of pure cultures of bacteria.'
688
+ br
689
+ e 'Pasteur discovered that microorganisms could
690
+ discriminate between optical isomers.'
691
+ br
692
+ e 'Proof that some microorganisms can cause disease
693
+ provided the greatest impetus for the development
694
+ of microbiology as an independent biological science.'
695
+ br
696
+ e "Kochs postulates link cause and effect in an infectious
697
+ disease."
698
+ br
699
+ e 'Richard Petri developed the transparent double-sided
700
+ "Petri dish" in 1887, which became the standard tool
701
+ for obtaining pure cultures.'
702
+ br
703
+ e "Koch's crowning scientific accomplishment was his
704
+ <b>discovery of the causative agent of tuberculosis</b>."
705
+ br
706
+ e 'The bacterium that causes tuberculosis, Mycobacterium
707
+ ­tuberculosis, is very difficult to stain because M.
708
+ tuberculosis cells contain large amounts of a waxlike
709
+ lipid in their cell walls.'
710
+ br
711
+ e 'Beijerinck devised a precise chemically defined medium to
712
+ isolate rhizobia and prove that they are responsible for the
713
+ formation of the root nodules of legumes.'
714
+ br
715
+ e 'Chemolithotrophy is the oxidation of inorganic compounds
716
+ to yield energy.'
717
+ br
718
+ e 'Chemolithotrophic bacteria obtain their carbon from CO₂.'
719
+ br
720
+ e 'Microbiologists realized that the ability to grow bacteria
721
+ rapidly and in controlled laboratory conditions made them
722
+ excellent model systems in which to explore the fundamental
723
+ nature of life.'
724
+ br
725
+ e 'The use of microbes as metabolic model systems led to the
726
+ important discovery that certain macromolecules and biochemical
727
+ reactions are universal. If one is to understand their function
728
+ in one cell one may be able to understand their function in
729
+ all cells (to some extent).'
730
+ br
731
+ e "Griffith's experiment showed that bacteria can transfer
732
+ genetic information."
733
+ br
734
+ e 'The term "Monera" is an antiquated term used to refer to
735
+ prokaryotic cells.'
736
+ br
737
+ e 'The ability of microbiologists to culture the microbial
738
+ diversity that abounds in nature has lagged behind the
739
+ ability to detect this diversity in the lab, via molecular
740
+ techniques.'
741
+ br
742
+ e 'Bacteria typically have a length that ranges from 1
743
+ to 10 μm.'
744
+ br
745
+ e 'More than 90% of bacteria in cultivation belong to one of
746
+ only four phyla: <b>Actinobacteria</b>, <b>Firmicutes</b>,
747
+ <b>Proteobacteria</b>, and <b>Bacteroidetes</b>.'
748
+ br
749
+ e "- Prokaryotes catalyze unique and indispensable
750
+ transformations in the biogeochemical cycles of the
751
+ biosphere, produce important components of the earth's
752
+ atmosphere, and represent a large portion of life's
753
+ genetic diversity."
754
+ br
755
+ e 'The bacterium <b>Epulopiscium</b> reaches a length of
756
+ 700 μm.'
757
+ br
758
+ e 'Bacterial phyla are billions of years old and this
759
+ time has allowed for extensive diversification.'
760
+ br
761
+ e 'While Archaea are quite diverse in their physiology,
762
+ cultured isolates have less morphological diversity than
763
+ Bacteria.'
764
+ br
765
+ e 'Methanogens (<i>Archaea</i>) are common in the guts of
766
+ animals - including humans.'
767
+ br
768
+ e '<i>Thaumarchaeota</i> are important contributors to the
769
+ global nitrogen cycle.'
770
+ br
771
+ e 'The <b class="italic">nanoflagellates</b> are microbial
772
+ predators that can be as small as 2 μm long.'
773
+ br
774
+ e 'The bacterial flagellum rotates like a propeller and is
775
+ powered not by ATP but by the proton motive
776
+ force (PMF).'
777
+ br
778
+ e 'Genomic studies of motile Archaea revealed that the
779
+ archaellum does have a structural counterpart in
780
+ Bacteria: the <b>type IV pilus</b>.'
781
+ br
782
+ e 'Cell morphologies in bacteria form a continuum, with some
783
+ shapes, such as rods and cocci, being very common, whereas
784
+ others, such as spiral, budding, and filamentous shapes,
785
+ being less common.'
786
+ br
787
+ e 'Bacteria may have evolved an optimal cell shape in order
788
+ to maximize nutrient uptake for survival in nutrient-limiting
789
+ environments. This is in particular important for the
790
+ consideration of a high surface-to-volume ratio.'
791
+ br
792
+ e 'Thiomargarita namibiensis (a large sulfur chemolithotroph)
793
+ is presently the largest known of all prokaryotic cells.'
794
+ br
795
+ e 'How fast a prokaryotic cell can grow depends in part on
796
+ the rate at which it can exchange nutrients and waste
797
+ products with its environment.'
798
+ br
799
+ e 'Amoebae use phagocytosis to ingest their prey via
800
+ phagocytosis.'
801
+ br
802
+ e 'The lipids of Archaea contain <i>ether</i>.'
803
+ br
804
+ e 'The cytoplasmic membrane of Bacteria and Archaea plays
805
+ a major role in energy conservation.'
806
+ br
807
+ e 'The normal microflora is highly dependent on the
808
+ conditions to which an individual is exposed to.'
809
+ br
810
+ e 'The cell wall of Bacteria and Archaea functions
811
+ to prevent osmotic lysis and gives the cell its shape.'
812
+ br
813
+ e 'The cytoplasm of prokaryotic cells maintains a
814
+ high pressure that is comparable to the pressure of
815
+ an automobile tire.'
816
+ br
817
+ e 'The cell wall confers shape and rigidity onto the
818
+ bacterial cell.'
819
+ br
820
+ e 'Antibiotics such as the penicillins and cephalosporins,
821
+ target bacterial cell wall synthesis, leaving the cell
822
+ susceptible to osmotic lysis.'
823
+ br
824
+ e 'As much as 90% of the cell wall of a gram-positive
825
+ bacterium can consist of peptidoglycan.'
826
+ br
827
+ e 'Many gram-positive bacteria produce acidic molecules
828
+ called teichoic acids embedded in their cell wall.'
829
+ br
830
+ e 'Some <b>teichoic acids</b> are covalently bonded to membrane
831
+ lipids rather than to peptidoglycan, and these are called
832
+ <b>lipoteichoic acids</b>.'
833
+ br
834
+ e 'Many antibiotics that are clinically useful against
835
+ gram-positive bacterial pathogens show little to no
836
+ activity against gram-negative pathogens because
837
+ of their outer membrane.'
838
+ br
839
+ e 'Endotoxins can cause violent symptoms in humans. The
840
+ endotoxins produced by Salmonella and enteropathogenic
841
+ strains of E. coli transmitted in contaminated foods
842
+ are a classic example of this.'
843
+ br
844
+ e 'Bacterial chemoreceptors are proteins that govern
845
+ the <b>chemotaxis response</b>.'
846
+ br
847
+ e 'An example for a slime-forming species is the lactic acid
848
+ bacterium called <b>Leuconostoc</b>.'
849
+ br
850
+ e 'Surface polysaccharides assist in the attachment of
851
+ microorganisms to solid surfaces.'
852
+ br
853
+ e 'Prokaryotic cells often contain inclusions of one sort or
854
+ another. These inclusions function as energy reserves and may
855
+ functiona as carbon reservoirs or have other special functions.'
856
+ br
857
+ e 'The microbiological process of forming minerals is called
858
+ <b>biomineralization</b>.'
859
+ br
860
+ e 'Endospores function as survival structures.'
861
+ br
862
+ e 'Pentosen entstehen aus Hexosen unter Abspaltung eines
863
+ CO₂ Moleküls.'
864
+ br
865
+ e 'The ABC transporter uses a periplasmic binding protein
866
+ which has high affinity for the substrate.'
867
+ br
868
+ e 'Hopanoids strengthen (some) bacterial cell walls.'
869
+ br
870
+ e 'Many bacteria are capable of producing several different
871
+ sigma factors, each of which recognizes a different
872
+ promoter sequence.'
873
+ br
874
+ e 'Phototrophic purple bacteria make use of <b>scotophobotaxis</b>
875
+ in order to avoid entering darkened habitats.'
876
+ br
877
+ e 'Algae can trigger chemotactic movements of bacteria toward
878
+ the algal cell via the substances that they produce.'
879
+ br
880
+ e 'Upon a nutrient downshift, rRNA, tRNA and protein synthesis
881
+ temporarily cease in bacteria.'
882
+ br
883
+ e 'Mitochondria are of bacterial dimensions.'
884
+ br
885
+ e 'Alarmones rapidly accumulate during a shift down
886
+ from amino acid excess to amino acid starvation.'
887
+ br
888
+ e 'Endospores function as survival structures and enable
889
+ the microorganism to endure unfavorable growth
890
+ condition.'
891
+ br
892
+ e 'Microbial eukaryotes that contain hydrogenosomes
893
+ carry out a strictly fermentative metabolism.'
894
+ br
895
+ e 'The M. tuberculosis cell envelope provides a
896
+ formidable protective barrier against drugs, host
897
+ defence mechanism and antibiotics.'
898
+ br
899
+ e 'The best carbon source is used first by bacteria.'
900
+ br
901
+ e 'The cytoplasmic membrane acts as <b>a selective
902
+ permeability barrier</b>.'
903
+ br
904
+ e "A 'selective medium' used in microbiology will
905
+ contain compounds that inhibit the growth of
906
+ some microorganisms, but not others."
907
+ br
908
+ e 'In regards to natural transformation of bacteria: DNA
909
+ from closely related species has a much higher chance to
910
+ be incorporated and integrated into the bacterial
911
+ chromosome than unrelated DNA.'
912
+ br
913
+ e 'Phosphatase activity is typically slower than
914
+ phosphorylation activity - in chemotaxis at the least.'
915
+ br
916
+ e 'The energy stored in ATP can drive membrane transport
917
+ of nutrients.'
918
+ br
919
+ e '<b>Periplasmic binding proteins</b> display a
920
+ very high binding affinity for their respective
921
+ substrates.'
922
+ br
923
+ e 'Das Verändern eines Faktors in einer Kultur von
924
+ Bakterien kann die Wirkung eines anderen Faktors
925
+ für das Wachstum dieser Bakterien beeinflussen.'
926
+ br
927
+ e 'Gene expression changes in bacteria follow a "shift
928
+ down" or a "shift up" in regards to the nutrient
929
+ state.'
930
+ br
931
+ e 'Sterilization eliminates all microorganisms -
932
+ including endospores.'
933
+ br
934
+ e 'The metabolic capacities of microbes differ.'
935
+ br
936
+ e 'The microbiome can be defined as the community
937
+ of microorganisms that live in a particular environment.'
938
+ br
939
+ e 'High GC contents are characteristic for microbes living
940
+ under extreme temperature conditions.'
941
+ br
942
+ e 'The Calvin cycle is the major biochemical pathway by
943
+ which phototrophic organisms incorporate CO₂ into
944
+ cell material.'
945
+ br
946
+ e "Bacteria called Clostridium perfringens and Vibrio
947
+ natriegens are among the world's fastest doublers,
948
+ reproducing in seven to ten minutes respectively."
949
+ br
950
+ e 'The bacterium <i>Staphylococcus aureus</i> kills an average
951
+ of about 100,000 Americans per year, more than any other
952
+ single microorganism.'
953
+ br
954
+ e 'Even bacteria suffer infection, aka phages that infect them
955
+ and inject their DNA/RNA into these bacteria.'
956
+ br
957
+ e 'The genome size of <b>Mesorhizobium loti</b> is more than
958
+ 7 million bp.'
959
+ br
960
+ e 'The war with bacteria will never end.'
961
+ br
962
+ e 'Auf besondere Situationen wie einen Hitzeschock oder
963
+ Nahrungsstress reagiert ein Bakterium, indem es mittels
964
+ anderer σ-Faktoren andere Promotoren erkennt und die
965
+ Gene selektiv anschaltet.'
966
+ br
967
+ e 'Nitrogen is an essential component of proteins, nucleic
968
+ acids and other cellular constituents, and as such it
969
+ is required in large amounts by living organisms.'
970
+ br
971
+ e '<b>Transport systems</b> move nutrients across phospholipid
972
+ bilayer membranes.'
973
+ br
974
+ e 'The survival and metabolism of any one group of organisms depends
975
+ on the survival and metabolism of other groups of organisms. For instance,
976
+ <b>metazoa</b> rely on microbial metabolism in order to survive.'
977
+ br
978
+ e 'We can assume a bacterium to contain information inside
979
+ (its genome) while being able to respond to external information
980
+ (e. g. signaling molecules or other information originating
981
+ from outside that bacterium).'
982
+ br
983
+ e '<b>Bacteria</b> are <b>extremely adaptable</b>.'
984
+ br
985
+ e 'Plasmide bieten Selektionsvorteile für ihre Wirte in ihren
986
+ Lebensräumen.'
987
+ br
988
+ e '<i>Rickettsia prowazekii</i> is the causative agent of epidemic
989
+ typhus.'
990
+ br
991
+ e 'The core proteome that defines the species.'
992
+ br
993
+ e 'Phenotypic diversity in prokaryotes (which refers primarily
994
+ to metabolic and ecological versatility) is achieved by varying
995
+ the proteome.'
996
+ }
997
+ # ========================================================================= #
998
+ # === Links
999
+ # ========================================================================= #
1000
+ h2 dot108?+
1001
+ 'Links'
1002
+ p('mars1em') {
1003
+ abr_self :local_genetics
1004
+ abr_self :local_biotechnology
1005
+ abr_self :local_cellbiology
1006
+ abr_self :local_cyanobacteria
1007
+ abr_self :local_synthetic_biology
1008
+ }
1009
+ }}