ch 10 Flashcards

(54 cards)

1
Q

bacteria is good for research bc

A
  1. fast growth
  2. small haploid genomes (mutations), excellent tools (plasmids), genetic info all coded the same way
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2
Q

mutation

A

any change in DNA (spontaneous and induced), leads to genetic variation

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3
Q

changes in DNA sequence are

A

spontaneous, mutagen, transposons, horizontal gene transfer

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4
Q

auxotroph

A

cannot produce all building blocks needed for life

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5
Q

prototroph

A

can make all building blocks for life

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6
Q

how to find mutations

A

direct selection, enrichment methods, screening methods (replica plating)

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7
Q

direct selection

A

picking something based on what it can do (antibiotic resistance)

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8
Q

enrichment method

A

the use of certain growth media to favor the growth of a particular microorganism over others

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9
Q

replica plating

A

the stamping one

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10
Q

mobile elements are caused by

A

transposase

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10
Q

mobile/ transposable elements, needs

A

move about the genome and inserts itself, disruptive, terminal inverted repeats

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11
Q

mobile elements can carry

A

extra genes

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12
Q

site directed mutagenesis

A

mutate a gene exactly how you want

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13
Q

site directed mutagenesis steps

A

start with PCR and modded primer, introduce to strain of interest, recombination

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14
Q

repair of mutation methods

A

photolyases, excision repair, recombinant repair, sos repair

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15
Q

horizontal gene transfer types

A

transformation, conjugation, transduction

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16
Q

vertical gene transfer

A

the passage of a plasmid from mother to daughter cells during division

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17
Q

horizontal gene transfer

A

gene transfer in same generation

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18
Q

transformation

A

DNA (naked) from the environment that is recombine with DNA, natural or artificial, needs competent cells

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19
Q

transduction

A

DNA transacting particles transfer from bacteriophage,
generalized- any
specialized - specific

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20
Q

conjugation

A

DNA transfer with contact, bn donor (plasmid) and plasmid, pop mating types,

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21
Q

competent cells

A

alteration in the cell wall that make it permeable to large DNA molecules

22
Q

recA protein

A

transformation protein that helps with recombinant

23
Q

donor DNA from

A

dead cells, quorum sensing biofilms

24
competent cell generation
chemical (calcium treatment and heat shock), eletroporation
25
generalized transduction
all genes are equally likely to be transferred
26
phage relipcation, lytic/ virulent
makes hella viral chromes, cell lysis, cell dies
27
phage relipcation, temperate
inserted into host chromie (prophage), will jump out and lyse the cell when signaled to, death unnecessary
28
lysogen at - site
ATT
29
P22 bacteriophage
circular genome, can undergo rolling circle to replicate, infect salmonella, can get DNA recomb'd into genome
30
-% of p22 progeny have host genome particles
2
31
specialized transduction
transfer certain genes, due to excision errors in prophage (lysogenic to lytic) DNA,
32
specialized transduction is found in - phages
temperate
33
attB site
insertion of prophage
34
specialized transduction gal x gal
when when prophage with gal gene insert itself into a host with the gal gene too, unstable
35
specialized transduction gal x gal-
when when prophage with gal gene insert itself into a host without the gal gene too, gal is inherited and its it stable
36
conjugation donor and recipient
can be diff species, bacteria and euk
37
conjugative plasmid
carries genes for sex pili and transfer plasmid (f factor)
38
dissimilation plasmid
encode enzymes for catabolism of unusual compounds
39
r factors
encode resistance encoding genes (to antibiotics, heavy metals, and toxins)
40
Hfr f plasmid is located
in chromosome
41
gram postive conjugation
no pili, via clumping and use secretion to transfer DNA
42
e faecalis
gram pos conjugation
43
crisper original use
prokaryotic response to bacteriophage, cuts up foreign DNA
44
cas
cleaves foreign DNA
45
CRISPERs
cleaved DNA within organized clusters "archive"
46
palindromic are needed in crispr why
a group of enzymes recognize certain repeats, and break the DNA there to insert important information in the middle
47
spacers
complementary sequence fo foreign DNA
48
crispr other uses
downreg expression of genes, adaptive immunity, stress responses (repair), immunize bacteria, genetic engineering
49
CRISPR is transcribed as
a long precursor RNA (pre- crRNA)
50
CIRSPR can treat
sickle cell
51
Genetic Differences between prokaryotes and eukaryotes
-DNA exchange not prerequisite for reproduction in prokaryotes. - If DNA exchange occurs, only small section of DNA exchange in prokaryotes. - DNA exchange in prokaryotes lots - only one in Eukaryotes - Prokaryotes haploid bigger
52
Phylogenetic analysis
Relatedness / Similarity of organisms
53
Phylogenetic analysis used for
Tracking sources of epidemics –disease epidemiology – Changes in microbes over time