BISC209/S12:Assignments: Difference between revisions

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| Compare your culture dependent and culture dependent estimations of the CFUs/gram of soil (dry wt) calculated in LAB 2 and think about the disparity. (DO NOT explain the discrepancy by criticizing your execution of the experiments!) Write a draft '''Introduction''' section of your final paper that includes a discussion of the "Great Plate Count Anomaly". Be sure to read the full directions for this assignment found at: Lab 2 Assignment: [[BISC209/S12: Assignment_209_Lab2 | Assignment: Introduction]].  
| Write a draft '''Introduction''' section of your final paper that includes a discussion of the "Great Plate Count Anomaly". Be sure to read the full directions for this assignment found at: Lab 2 Assignment: [[BISC209/S12: Assignment_209_Lab2 | Assignment: Introduction]].  
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| Construct a table (with properly formatted legend) of your experimental evidence for the abundance of microorganisms in your soil community. Write a draft results section. Consult the full directions for this assignment found at: [[BISC209:Assignment_209_Lab3 | Lab 3 Assignment: Colony Count vs. Direct Count Enumeration]]
| Compare your culture dependent and culture dependent estimations of the CFUs/gram of soil (dry wt) calculated in LAB 2 and think about the disparity. Construct a table (with properly formatted legend) of your experimental evidence for the abundance of microorganisms in your soil community (2.5 points). Write a draft results section (5 points). Consult the full directions for this assignment found at: [[BISC209:Assignment_209_Lab3 | Lab 3 Assignment: Colony Count vs. Direct Count Enumeration]]
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| '''5'''
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| Analyze prevalence of microbial starch & cellulose digesters and phosphate solubilizers in the soil community. Analyze CLPP data for carbon source utilization; turn in spreadsheet with calculations and make graphs turned into figures with legends. More information about how to use your data in these calculations can be found at [[BISC209/S12: Assignment_209_BIOLOG]]  Full directions and useful references can be found at  Lab 4 Assignment:  [[BISC209/S12: Assignment_209_ Lab4 | Assignment: Results Section Community Level Assessments]]
| Analyze your community level diversity and behavior data including the prevalence of microbial starch & cellulose digesters and phosphate solubilizers in the soil community and the carbon source utilization patterns and CMD measurement. Write a results section with figures/tables and narrative. Full directions and useful references for this assignment can be found at  Lab 4 Assignment:  [[BISC209/S12: Assignment_209_BIOLOG]]
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| '''M&M''': Compose a draft of your Materials and Methods section of your final paper with the following three general sections:<br> 1)Community level physiological testing: carbon source profiling, exoenzymes profiling; <BR> 2) Identification of bacteria by 16S rRNA gene sequencing from soil genomic DNA;<br> 3) Selection and isolation of soil community bacteria to pure culture. More information can be found at Lab 5 Assignment:  [[BISC209/S12: Assignment_209_Lab5 | Materials & Methods]]
| '''M&M''': Compose a draft of your Materials and Methods section of your final paper with the following three general sections:<br> 1)Community level physiological testing: carbon source profiling, exoenzymes profiling; <BR> 2) Identification of bacteria by 16S rRNA gene sequencing;<br> 3) Selection and isolation of soil community bacteria to pure culture.<BR> More information can be found at Lab 5 Assignment:  [[BISC209/S12: Assignment_209_Lab5 | Materials & Methods]]
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! 6
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| Write a brief summary of the theory behind the following techniques that we used to identify our bacterial species by molecular tools:  genomic DNA isolation, polymerase chain amplification of part of the 16s rRNA genes, use of the Zero Blunt® TOPO® PCR Cloning Kit to create a library of unique plasmid vector with our 16S rRNA gene inserts and then select, One Shot® TOP10 Competent E. coli Cells that allowed us to select and separate our 16S rRNA genes for sequencing, and DNA sequencing by the newer fluorescent-labeled ddNPTs chain -termination (Sanger) method. Directions found at: Lab 6 Assignment:  [[BISC209/S12: Assignment_209_Lab6 | Assignment: Theory Summary ]]
| Write a brief summary of the theory behind the following techniques that we used to identify our bacterial species by molecular tools:  polymerase chain amplification of the 16srRNA gene and DNA sequencing by the newer fluorescent-labeled ddNPTs chain -termination (Sanger) method. Directions found at: Lab 6 Assignment:  [[BISC209/S12: Assignment_209_Lab6 | Assignment: Theory Summary ]]
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| '''Partial Results section with figures/tables: '''Richness and Community Behavoir in a Microbial Soil Community''' using as evidence the results from the community level assays of functional metabolic diversity in carbon source utilization and amalyase, cellulase, and phosphate solubilizing exoezyme prevalence. Read more about this assignment at: [[BISC209/S12: Assignment_209_Lab7 | Assignment: Partial Results II with Fig/Tables]]
| '''Discussion Outline''', '''Annotated Bibliography''' of appropriate references for the discussion section of your paper (5 points)<BR>'''Graphical abstract''' draft (2.5 points): See models in research reports found in recent issues of the journal ''Cell''. A description and examples of Graphical Abstracts can be found at http://www.elsevier.com/wps/find/authorsview.authors/graphicalabstracts [http://www.elsevier.com/wps/find/authorsview.authors/graphicalabstracts]. More information on this assignment found at: [[BISC209/S12: Assignment_209_Lab7 | Assignment: Annotated Bibliography/Graphical Abstract]]
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| '''Make a table of the tests performed on the isolates from your soil community''' (your isolates and your teammates from the same sampling site) and write a complete results narrative. You should include in the table: Gram stain, description of the colony morphology, description of the individual bacteria and any characteristic arrangement (cocci, rods, with descriptors ie., large, small, bullet shaped, in chains, etc.), evidence of spores (either endospore stain positive or visualization of empty areas in vegetative cells on Gram stain), antibiotic production, motility, evidence for nitrogen cycling capabilities . Make a separate figure from a photograph of your interactions assay and analyze those data. <BR>'''Graphical abstract''': See models in research reports found in recent issues of the journal ''Cell''. <BR> A description and examples of Graphical Abstracts can be found at http://www.elsevier.com/wps/find/authorsview.authors/graphicalabstracts [http://www.elsevier.com/wps/find/authorsview.authors/graphicalabstracts]. More information on this assignment found at: [[BISC209/S12: Assignment_209_Lab9 | Assignment: Graphical Abstract/Complete Results]]
|'''Study for Lab practical'''
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| '''Study for Lab practical.'''
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| '''Lab practical'''  
| '''Lab practical'''  
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| '''Write a draft results section of your work on your isolates.''' Construct a table of the tests performed on the isolates from your soil community (your isolates and your teammates from the same sampling site) and write a complete results narrative. You should include in the table: Gram stain, description of the colony morphology, description of the individual bacteria's structural characteristics including shape & arrangement (cocci, rods, with descriptors ie., large, small, bullet shaped, in chains, etc.), evidence of spores (either endospore stain positive or visualization of empty areas in vegetative cells on Gram stain), motility, etc. Include test results that you will use as evidence for metabolic diversity or community behavior, ie. nitrogen cycling capabilities, fermentation of mannitol, etc. Make separate figures from photographs of the interactions assays for your soil sample and another from a photo of a positive antibiotic production assay (if your soil sample showed such a positive) and analyze those data in your narrative. Post your table to the Data folder for each soil sampling site so your classmates can access and use this information for the other bacterial members of each soil community.
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| '''April 24 or 25'''
| '''Group Presentation'''<BR> Note that the 25pt includes 10 points of Individual Contribution to Group points--assigned by consensus of your project and presentation group
| '''Final Paper''': Information found at: [[BISC209/S12: Assignment_209_Lab10 | Assignment: Final Paper]]
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|'''Final Paper''': Information found at: [[BISC209/S12: Assignment_209_Lab12 | Assignment: Final Paper]]
|'''Group Presentation'''<BR> Note that the 15pt includes points of Individual Contribution to Group points--assigned by consensus of your presentation group. Information found in Resources in Sakai (folder Group Presentation) and in Lab 12 in the wiki at [[BISC209/S12: Lab12|LAB12 | Group Presentation]].
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==Assignments==
==Assignments==
Lab 1 Assignment: [[BISC209/S12: Assignment_209_Lab1 | Assignment: Enrichment for culturable bacteria of specific groups]]<BR>
Lab 1 Assignment: [[BISC209/S12: Assignment_209_Lab1 | Assignment: Enrichment/Selection/Differentiation of Culturable Bacteria]]<BR>
Lab 2 Assignment:  [[BISC209/S12: Assignment_209_Lab2 | Assignment: Introduction]]<BR>
Lab 2 Assignment:  [[BISC209/S12: Assignment_209_Lab2 | Assignment: Introduction]]<BR>
Lab 3 Assignment: [[BISC209/S12: Assignment_209_Lab3 | Assignment: Colony Count vs. Direct Count Enumeration]] <BR>
Lab 3 Assignment: [[BISC209:Assignment_209_Lab3 | Lab 3 Assignment: Colony Count vs. Direct Count Enumeration]]<BR>
Lab 4 Assignment:  [[BISC209/S12: Assignment_209_ Lab4 | Assignment: Results Section Community Level Assessments]]<BR>
Lab 4 Assignment:  [[BISC209/S12: Assignment_209_BIOLOG]]<BR>
Lab 5 Assignment:  [[BISC209/S12: Assignment_209_Lab5 | Assignment: Materials & Methods]]<BR>
Lab 5 Assignment:  [[BISC209/S12: Assignment_209_Lab5 | Assignment: Materials & Methods]]<BR>
Lab 6 Assignment:  [[BISC209/S12: Assignment_209_Lab6 | Assignment: Theory Summary ]]<BR>
Lab 6 Assignment:  [[BISC209/S12: Assignment_209_Lab6 | Assignment: Theory Summary ]]<BR>
Lab 7 Assignment: [[BISC209/S12: Assignment_209_Lab7 | Assignment: Partial Results section with Fig/Tables]]<BR>
Lab 7 Assignment: [[BISC209/S12: Assignment_209_Lab7 | Assignment: Annotated Bibliography/Graphical Abstract]]<BR>
Lab 9 Assignment: [[BISC209/S12: Assignment_209_Lab9 | Assignment: Graphical Abstract]]<br>
Lab 10 Assignment: [[BISC209/S12: Assignment_209_Lab10 | Assignment: Final Paper]]<br>
Lab 12 Assignment: [[BISC209/S12: Assignment_209_Lab12 | Assignment: Final Paper]]<br>
 
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Latest revision as of 06:16, 26 March 2012

Wellesley College-BISC 209 Microbiology -Spring 2012

Graded Lab Assignments

Lab Assigned Lab Due Assignment
description
Point Value
(Total 200)
1 2 Turn in at the beginning of Lab 2, a Discussion with References of how the enrichment culture techniques and media you will use will select soil bacteria of the specific groups we seek and differentiate them from other microbes in the community. Be sure to read the directions for this assignment found at: Assignment: Enrichment/Selection/Differentiation of Culturable Bacteria. 10
2 3 Write a draft Introduction section of your final paper that includes a discussion of the "Great Plate Count Anomaly". Be sure to read the full directions for this assignment found at: Lab 2 Assignment: Assignment: Introduction. 5
3 4 Compare your culture dependent and culture dependent estimations of the CFUs/gram of soil (dry wt) calculated in LAB 2 and think about the disparity. Construct a table (with properly formatted legend) of your experimental evidence for the abundance of microorganisms in your soil community (2.5 points). Write a draft results section (5 points). Consult the full directions for this assignment found at: Lab 3 Assignment: Colony Count vs. Direct Count Enumeration 7.5
4 5 Analyze your community level diversity and behavior data including the prevalence of microbial starch & cellulose digesters and phosphate solubilizers in the soil community and the carbon source utilization patterns and CMD measurement. Write a results section with figures/tables and narrative. Full directions and useful references for this assignment can be found at Lab 4 Assignment: BISC209/S12: Assignment_209_BIOLOG 10
5 6 M&M: Compose a draft of your Materials and Methods section of your final paper with the following three general sections:
1)Community level physiological testing: carbon source profiling, exoenzymes profiling;
2) Identification of bacteria by 16S rRNA gene sequencing;
3) Selection and isolation of soil community bacteria to pure culture.
More information can be found at Lab 5 Assignment: Materials & Methods
10
6 7 Write a brief summary of the theory behind the following techniques that we used to identify our bacterial species by molecular tools: polymerase chain amplification of the 16srRNA gene and DNA sequencing by the newer fluorescent-labeled ddNPTs chain -termination (Sanger) method. Directions found at: Lab 6 Assignment: Assignment: Theory Summary 10
7 8 Discussion Outline, Annotated Bibliography of appropriate references for the discussion section of your paper (5 points)
Graphical abstract draft (2.5 points): See models in research reports found in recent issues of the journal Cell. A description and examples of Graphical Abstracts can be found at http://www.elsevier.com/wps/find/authorsview.authors/graphicalabstracts [1]. More information on this assignment found at: Assignment: Annotated Bibliography/Graphical Abstract
7.5
8 9 Study for Lab practical
9 9 Lab practical 45
9 10 Write a draft results section of your work on your isolates. Construct a table of the tests performed on the isolates from your soil community (your isolates and your teammates from the same sampling site) and write a complete results narrative. You should include in the table: Gram stain, description of the colony morphology, description of the individual bacteria's structural characteristics including shape & arrangement (cocci, rods, with descriptors ie., large, small, bullet shaped, in chains, etc.), evidence of spores (either endospore stain positive or visualization of empty areas in vegetative cells on Gram stain), motility, etc. Include test results that you will use as evidence for metabolic diversity or community behavior, ie. nitrogen cycling capabilities, fermentation of mannitol, etc. Make separate figures from photographs of the interactions assays for your soil sample and another from a photo of a positive antibiotic production assay (if your soil sample showed such a positive) and analyze those data in your narrative. Post your table to the Data folder for each soil sampling site so your classmates can access and use this information for the other bacterial members of each soil community. 10
10 April 24 or 25 Final Paper: Information found at: Assignment: Final Paper 60
11 12 Lab notebook 5
11 12 Group Presentation
Note that the 15pt includes points of Individual Contribution to Group points--assigned by consensus of your presentation group. Information found in Resources in Sakai (folder Group Presentation) and in Lab 12 in the wiki at LAB12 | Group Presentation.
15
Other CLEAN-UP points 5


Assignments

Lab 1 Assignment: Assignment: Enrichment/Selection/Differentiation of Culturable Bacteria
Lab 2 Assignment: Assignment: Introduction
Lab 3 Assignment: Lab 3 Assignment: Colony Count vs. Direct Count Enumeration
Lab 4 Assignment: BISC209/S12: Assignment_209_BIOLOG
Lab 5 Assignment: Assignment: Materials & Methods
Lab 6 Assignment: Assignment: Theory Summary
Lab 7 Assignment: Assignment: Annotated Bibliography/Graphical Abstract
Lab 10 Assignment: Assignment: Final Paper