Lab Report 2 - General Microbiology-merged

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School

Rutgers University, Newark *

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Course

120:335

Subject

Biology

Date

May 1, 2024

Type

pdf

Pages

10

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Introduction: We had two different labs: differential media and quantification of bacterial population. For the differential media, the goal was to see which media the bacteria can ferment in and strive in. This would be helpful for when we want to have a successful bacterial colony. There are four different outcomes; acid production, gas production, alcohol production, and finally peptone deamination, which happens when there is no sugar fermentation. For the quantification of bacterial population, our goal was to study the most efficient and accurate way to count bacterial colony in a medium. There are two main ways to count bacterial colonies: viable count and direct count, each have their own pros and cons. As for viable count, it is the most accurate one, it consists of different dilutions from different stocks, and it is counted. For direct count, we use a cellomere, and it is not as accurate, but it is significantly easier than the first. However, both dead and alive bacteria are counted since everything is stained. Results: Please refer to data sheets and pictures. Discussion: Ex. 6-1: We looked at the the bacteria in the diluted plates for the viable count. We had bacteria in dilutions of 10^-4, 10^-5, 10^-6, and 10^-7. There were only growths in 10^-6 and 10^-4, with 10^-6 significantly less. The conclusion we ended with is that there was an error during lab, and we mixed 10^-5 with 10^-6. Ex. 6-3: There was bacteria diluted. The bacteria were then injected to a cellomere using pipettes and were counted using a microscope. The numbers of bacteria were 389 and 223, with the calculated cell density being 2.4E9 and 1.4E9, respectfully. Ex. 5-3: We used the phenol red broths technique to see whether the bacteria can ferment the sugars or not. There was either/or acid/gas production, alcohol production, or no sugar fermentation. Yellow broth means there was fermentation that occurred, while red means there were no fermentation. Moreover, if there was a gas inside the glass, then this indicates that there was fermentation with gas production. Ex. 5-4: The methyl red vogus-proskauer was a lab that is used to indicate fermentation and acid production. Color changes for both tubes indicated positive results. Ex. 5-10: This lab helped us to examine whether the bacteria was positive for malonate utilization or not. Klebsiella (Enterobacter) aerogenes was able to utilize malonate. Escherichia coli was unable to utilize malonate.
Ex. 5-20: Finally, for this lab, we were able to observe whether the bacteria was able to reduce sulfur or not. The enzymes Cysteine desulferase and/or Thiosulfate reductase are used to produce H2S gas. Black precipitate from Ferrous Ammonium Sulfide binding to the H2S gas indicated positive results. E. coli was unable to reduce sulfur, while C. freundii was able to reduce sulfur, and thus turning black.
6-1 6-3 5-3 5-4 5-10 5-20
280 106 = 2 . 8 E
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