Lecture 2: Taxonomy and Biodiversity Flashcards

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1
Q

What is taxonomy

A

A method of classifying organisms based on ancestry

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2
Q

What is classical taxonomy and how did it classify organisms

A

An old method of classifying organisms based on phenotype

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3
Q

What is molecular taxonomy and how does it classify organisms

A

A modern approach to classifying organisms base on genotype

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4
Q

What are the 3 main parts of taxonomy

A
  1. Classification (arrangement of organisms based on similarity)
  2. Nomenclature (naming organisms)
  3. Identification (determining whether an organism belong to the group which it is classified and named)
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5
Q

What is microbial diversity

A

The NUMBER and ABUNDANCE of species/kinds of organisms in a community

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6
Q

How did classical taxonomy ‘correctly’ classify/identify organisms

A

Scoring of characteristics/phenotypes as 1 (trait positive) or 0 (trait negative).
Therefore, the more similarities between organisms, the more related they are

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7
Q

What are Analytical Process Index (“API”) Strips

A

test strips with various wells containing different conditions for bacterial suspension (inferring bacterial properties).

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8
Q

What are pros and cons of API strips

A

+ Quick and easy
+ can be designed for specific bacteria; disease diagnosis
+ doesn’t require much training
- not as detailed as molecular analysis

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9
Q

What is a dendrogram? Whys is it different to a phytogenic tree?

A

Dendrograms illustrate the degree of relation between organisms by grouping particular traits. Unlike a phytogenic tree, the branches of dendrograms do not insinuate and genetic ‘distance’ from each other

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10
Q

How does molecular taxonomy use genomes?

A

In current times, due to limitations in sequencing technology, whole genomes aren’t often sequenced and instead smaller conserved regions are, such as rRNA genes

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11
Q

What are the differences between prokaryote and eukaryotes ribosomes

A

Euk vs prok

60s+40s=80s 50s+30s=70s

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12
Q

What is 16s rRNA and what is its significance?

A

It is a component of the prokaryotic 30s (small) subunit. It is present in every cell and it ~1550bps long with 1-25 copies of this gene in cells.

Some sections are highly conserved (structural elements) others are more variable

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13
Q

What is an example of 2 variable regions within the 16s gene? what is their significance?

A

V3; 341F/529R and V4; 515F/806R (3rd and 4th variable regions).
nF/nR =forward and reverse primers at that nucleotide.

The 5’ and 3’ ends of these two regions are highly conserved, whereas the central regions are variable

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14
Q

How can the 16s infer genomic relation?

A

Based on the number of similar or different bases down lineages within the 16s gene, level or diversion/relation can be inferred between organisms.

percentage of relation can then be calculated

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15
Q

What is the problem with relying on a single gene to infer whole genome/specie relations?

A

Variations in other genes may be far higher/lower than the 16s region, meaning organisms may realistically be more/less related tan the 16s region suggests

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16
Q

What do phylogenetic trees do?

A

Align homologous sequences and look at the frequency of differences between them to generate a tree

17
Q

what are the two methods of generating phylogenetic trees?

A

Maximum parsimony and maximal likelihood

18
Q

What is maximal parsimony?

A

Looks to generate a phylogenetic tree with the fewest possible branches. seeks to limit the amount of homoplasy (i.e., convergent-, parallel evolution, evolutionary reversals)

Keep it simple

Con = more than one tree may produce results consistent with the data

19
Q

What is maximal likelihood?

A

Based on statistical calculations. For each possible tree, the program calculates the likelihood (probability) that such tree would produce observed data

pro: produces just one tree

20
Q

What are the two main methods of studying diversity

A

Operational Taxonomic Unit (OTU) and Metagenomics

21
Q

What is operational taxonomic unit?

A

Used to classify groups of closely related individuals.

Clusters sequences (e.g., 16s rRNA) based on their similarity, a threshold of 97% or higher is often required to create an OTU. Organisms of 98.65% or more similarity may (or may not) be of the same species.
 OTUs = clusters of organisms of varied levels of similarity

CAN THEN BE USED TO WORK OUT DIVERSITY WITHIN A POPULATION

Con; charts don’t state n-size, just abundance

22
Q

What is metagenomics and how is it used here

A

study of a collection or genetic material. mapping the genomes/genes according to their abundance in a population