Answer:
- Can leverage Next Generation Sequencing technology to identify and characterize organisms
- Has resources to support analysis at the DOE-JGI site.
- Can identify microbiologic organisms without traditional isolation and culturing of individual organisms.
Explanation:
Metagenomics can be defined as the study of whole genomes of biological communities recovered from environmental samples. This genomic field has enabled the discovery of new species (microorganisms) and their effects on the environment. Next-Generation Sequencing (NGS) technologies allow to obtain huge amounts of genomic data, which has been a limitation in genomics and metagenomics. Metagenomic NGS (mNGS) is a technique used for sequencing nucleic acids present in a biological sample containing mixed populations of microorganisms. Finally, the Department of Energy Joint Genome Institute (DOE JGI) is a referent in metagenomic analysis, especially in genome assembly data obtained from microbial communities. This Science User Facility has developed a series of bioinformatics tools and databases in order to analyze metagenomic information.
Answer:
Option D is correct
Explanation:
Luria broth contains yeast concentrate so it would show a marked B- galactosidase activity which is an enzyme that catalyzes the hydrolysis of B- galactosides including lactose and it is the first step of lactose fermentation.
Answer:
The leading strand is continuously synthesized and is elongated during this process to expose the template that is used for the lagging strand (Okazaki fragments). During the process of DNA replication, DNA and RNA primers are removed from the lagging strand of DNA to allow Okazaki fragments to bind to.
Explanation:
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Answer:
In acid-fast staining, carbon fuchsin is used as a primary stain which dissolves the mycolic acid present in the cell wall of <em>Mycobacterium smegmatis </em>and penetrates through it which results in staining <em>Mycobacterium</em> red.
Staphylococcus aureus cell wall does not contain mycolic acid so carbon fuchsin does not penetrate its cell wall, therefore, it becomes colorless after destaining with acid alcohol.
After destaining step methylene blue is added to stain non-acid-fast bacteria blue. So if I mistakenly forgot to use methylene blue during the procedure <em>Mycobacterium smegmatis</em> will appear red due to carbon fuchsin present in their cell wall and S<em>taphylococcus aureus</em> will appear colorless because it is destained.
Answer:
The cell cycle has three phases that must occur before mitosis, or cell division, happens. These three phases are collectively known as interphase. They are G1, S, and G2. The G stands for gap and the S stands for synthesis.
Explanation: