Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- Much of what we know about the human microbiome – the microbial communities associated with various parts of our bodies – comes from genome sequencing. Here, DNA is extracted from all cells in samples collected from various body sites and randomly sequenced, typically generating huge volumes of short-read sequencing data. These reads thus represent a random, mixed snapshot of genes encoded within any cell in the original sample. As human cells are commonly collected along with the bacteria, researchers first remove human DNA sequences from the dataset. To do this, they computationally remove any reads that are highly similar to the human reference genome; the remaining gene sequences are then assumed to belong to the microbial community. Researchers studying the human microbiome have frequently been interested to find that these bacterial communities seem to contain a number of highly unusual genes that are unique to human-associated microbes. a) Briefly describe one feature of…arrow_forwardOrder the following technical steps that are required to identify a bacterium by PCR and sequencing of the 16S rRNA gene. [1 mark] - Carry out thermal cycling (amplification) of the PCR - Checking the PCR product (amplication) by agarose gel electrophoresis - Purify the PCR product - Perform a DNA extraction - Sequence the PCR product(Sanger sequencing) - Grow a fresh overnigh liquid culture - Obtain a pure bacterial culture - Set up a 16S Rrna gene PCR - Perform bioinformatic analysis (BLAST)arrow_forwardCompare the possible differences between a eukaryotic protein-encoding gene cloned by PCR and the same gene cloned by reverse transcriptase PCR (RT–PCR).arrow_forward
- CRISPR-cas9 is a powerful technique for gene editing. Please place the stages of a CRISPR-cas9 gene editing workflow in the correct order below options are on the rightarrow_forward1) One of the first studies extracted all the DNA from a biofilm in an acid mine drainage in northern California in 2004. Then cloned the DNA in E. coli, sequenced all of the cloned fragments and then attempted to reconstruct the genomes of the different individuals in the population. This approach is an example of what? -Transcriptomics -Genomics -Metatranscriptomics -Metagenomics -Proteomicsarrow_forwardCategorize the following as being associated with transformation, conjugation, or transduction. Note that some items may be associated with more than one process. Transformation Conjugation Transduction requires a virus can transfer dead bacterium's DNA to a new host cell efficient way to get naked plasmid into E. coli cells in the lab involves a pilus describes type of horizontal gene transfer in bacteria cells need to be competent process exploitod by biotechnology transfer requires at least two living bacteria alters bacterial genomearrow_forward
- What are some limitations to using biochemical test as a classification method for bacterial species. What do you think some limitations of the 16s RNA sequencing for classifying bacterial species? explain why bacterial taxonomy is such a highly debated topicarrow_forwardEvaluate the paragraph below and drag the labels to complete the sentences that discuss antibiotic resistance gene locations?arrow_forwardSelect all the statements that provide evidence that DNA is the genetic material. Check All That Apply 1. By weight, a eukaryotic chromosome contains more protein than DNA. 2. Treatment of purified DNA with a DNA-degrading enzyme destroyed the ability of S bacteria to transform R bacteria. 3. The R mutant form of S. pneumonia does not cause infection in mice. 4. Radioactively-labeled DNA remained in bacterial cells after phage T2 infection. 5. Proteins are more complex than DNA because they are composed of 20 different amino acids. Pls help asap!! I am so confusedarrow_forward
- detail explaination asaparrow_forwardThe temperature at which the primers and target DNA hybridize may be changed to influence the stringency of PCR amplification. What effect will changing the hybridization temperature have on the amplification? Let's say you have a certain yeast gene A and want to check whether it has a human equivalent. How might managing the hybridization's rigor benefit you?arrow_forwardWhy is a thermostable form of DNA polymerase (e.g., Taqpolymerase) used in PCR? Is it necessary to use a thermostableform of DNA polymerase in the dideoxy method or in site-directedmutagenesis?arrow_forward
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