Topic 2 Flashcards

(36 cards)

1
Q

prokaryotes cell walls

A

murein

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2
Q

gram positive

structure
stain
example

A

thick layer of peptidoglycan in cell wall

stained purple/ blue

Staphyloccocus releases exotoxins

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3
Q

gram positive antibiotics

A

Beta-lactam antibiotics are effective as they inhibit enzymes involved in peptidoglycan layer formation e.g. penicillin

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4
Q

gram negative

structure
stain
example

A

thin layer of peptidoglycan between two layers of membrane

stain red

Salmonella releases endotoxins

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5
Q

gram negative antibiotics

A

Polypeptide antibiotics are effective as they interact with the phospholipid membrane and unable to cross thick peptidoglycan layer so not effective on gram positive

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6
Q

cigarette smoke damages cell membrane structure

A

made up of phospholipid, channel proteins and carrier proteins
affects transport of non-polar molecules e.g. O2
affects endocytosis and exocytosis
damage to channel/ carrier proteins alters shape and affects facilitated diffusion, transport of ions, polar molecules
damage to carrier proteins affects active transport
allows lysozymes to escape

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7
Q

measuring cells

A

calibrate an eye piece graticule using a stage micrometer
measure length
more than one measurement taken

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8
Q

DNA virus

example

A

DNA template for new DNA and mRNA

E.g. λ phage

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9
Q

RNA virus

A

Both have a helical capsid

Positive ssRNA with helix structure
Sense strand can translated directly and templates for mRNA forming new viral protein
E.g. tobacco mosaic virus

Negative ssRNA with helix structure, envelope
Antisense strand must be transcribed to a sense strand before being able to translated to template for mRNA forming new viral proteins
E.g. ebola virus

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10
Q

RNA retrovirus

A

Envelope
RNA synthesises the enzyme reverse transcriptase to convert DNA into RNA and new viral proteins which leaves the host cell by exocytosis
E.g. HIV

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11
Q

Lytic cycle (4)

A
  • Bacteriophage ATTACHES TO A BACTERIAL and its DNA is injected into the host cell, stimulating the synthesis of viral enzymes
  • Phage DNA inactivates the host DNA and takes over the cell biochemistry to REPLICATE PHAGE DNA
  • Protein coats form around phage DNA to form NEW PHAGE PARTICLES
  • Lysozyme is synthesised and released causing the bacterial cell to burst (LYSIS) and release many bacteriophages to infect other bacteria
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12
Q

Lysogenic pathway (latency) (4)

A
  • Bacteriophage attaches to a bacterial cell and its DNA is injected into the host cell, stimulating the synthesis of viral enzymes
  • Viral DNA is incorporated with host cell DNA so it divides when the host cell DNA divides
  • Protein coats form around phage DNA to form new phage particles
  • Lysozyme is synthesised and released causing the bacterial cell to burst and release many bacteriophages to infect other bacteria
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13
Q

how do antivirals work (2)

A

inhibiting virus replication

Target receptors of virus used to recognise host cells
Target enzymes involved in translation and replication of new viral DNA/ RNA

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14
Q

how do viruses work

A

Lysis of host cells
Protein coat can act as a toxin
Some virus cause host cells to make toxins

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15
Q

why is mitosis useful

A

for growth/ repair of cells

requires genetically identical cells

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16
Q

interphase

A

G1: Time between cytokinesis and chromosome duplication

S: DNA synthesis so amount of chromatin doubles forms new chromatids (same number of chromosomes) and spindle proteins are synthesised

G2: Organelles and other materials double (by protein synthesis)

17
Q

prophase

A

Chromosomes become visible as they shorten and thicken

Centrioles move to opposite poles of the cell and spindle fibres develop

Nuclear envelope breaks down leaving chromosomes free in the cytoplasm

18
Q

metaphase

A

Spindle fibres attach to the centromere of every chromosome so they line up across the equator of the spindle

19
Q

anaphase

A

Centromere splits so sister chromatids divide, spindle fibres contract and pull chromatids to opposite poles

20
Q

telophase

A

Chromosomes group together at each pole and a nuclear envelop forms around each group so nuclei are present
Chromosomes decondense to form chromatin, spindle fibres break down

21
Q

cytokinesis

A

cytoplasm splits to form two genetically identical daughter cells

22
Q

advantage of meiosis

A

genetic variation enables species to survive changes to the environment

enables contribution of alleles from two individuals

23
Q

independent segregation

A

in metaphase I, random arrangement of maternal and paternal chromosomes from homologous pair go to either two new cells forms new combinations of maternal and paternal chromosomes

24
Q

crossing over

A

in prophase I, exchange of alleles between non-sister chromatids forms new combinations of alleles

homologous chromosomes pair up, chiasmata form, break in chromatid, genetic information exchanged between chromatids

25
mutation changes primary structure of enzyme so explain why the heck it would change enzyme activity
different sequence of amino acids different R groups change in ionic, hydrogen bonding, sulphur bridges change in shape of active site so change in enzyme activity
26
translocation
a piece of chromosome from a homologous pair of chromosomes breaks off and joins onto to a non-homologous chromosome from a different pair of chromosomes
27
non-disjunction
a homologous pair of chromosomes do not separate during anaphase 2 so one gamete has two copies of the chromosome and the other will have none monosomy: one copy of one chromosome polysomy: more than two copies of one chromosome
28
oogenesis
* Primordial germ cell divides by mitosis to form (diploid) oogonia * One oogonia grows into a primary oocyte * First meiotic division occurs forming one (haploid) secondary oocyte and one first polar body * After fertilisation, second meiotic division of the secondary oocyte occurs forming an ovum and a polar body, the first polar body divides to form two polar bodies
29
spermatogenesis
* Primordial germ cell divides by mitosis to form (diploid) spermatogonia * One spermatogonia grows into a primary spermatocyte * First meiotic division occurs forming two (haploid) secondary spermatocytes * Second meiotic division of the two cells forms four spermatids * Spermatids differentiate in the testes to form spermatozoa capable of fertilising an ovum
30
difference between products of oogenesis and spermatogenesis
ova is larger, surrounded by zona pellucida, spermatozoa do not spermatozoa contain an acrosome, have a flagellum, ova do not oogenesis produces polar bodies, spermatogenesis do not
31
fertilisation
* Sperm reaches secondary oocyte and acrosome reaction is triggered by receptors on zona pellucida causing the acrosome to open and release enzymes to digest the zona pellucida * Membranes of the sperm and secondary oocyte fuse * Second meiotic division of the secondary oocyte occurs forming an ovum * Ion channels in the ovum open so is positively charged to prevent other sperm entering * Cortical granules move to ovum membrane and leave by exocytosis, secretes contents into zona pellucida forming fertilisation membrane * Head of the sperm enters (tail left outside), absorbs water, swells and bursts, releasing chromosomes to fuse with ovum nucleus forming a diploid zygote
32
embryo to blastocyst
* Cleavage occurs (cells divide rapidly by mitosis without G2 interphase) to increase number of cells * Cells are all genetically identical and diploid * Cells become smaller (amount of organelles and cytoplasm is halved with each cell division) and form a thin layer surrounding a fluid filled cavity in the structure of a hollow sphere called a blastocyst
33
formation of pollen grains
in anther • many (diploid) microspore mother cells divide by meiosis to form (haploid) microspores • Microspores divide by mitosis to form pollen grains, each containing a (haploid) tube nucleus and a (haploid) generative nucleus Tube nucleus forms the pollen tube Generative nucleus divides by mitosis forming male nuclei and one will fuse with the ovum to form a new plant
34
formation of ovum
in embryonic sac • (diploid) Megaspore mother cells divide by meiosis to form four (haploid) megaspores (three of which degenerate) • One megaspore has three mitotic divisions to form an embryonic sac containing an ova, two polar nuclei, synergids and antipodal cells
35
plant fertilisation
* Pollen grain lands on the stigma during pollination and breaks down proteins in the style using hydrolytic enzymes, growing a towards the micropyle * Generative nucleus passes down and divides by mitosis to form two (haploid) male nuclei gametes * Pollen tube passes through the ovary to reach an ovule and passes through the micropyle, allowing for the two male nuclei to fertilise the ovule * Double fertilisation: Inside the embryonic sac, one male nucleus fuses with two polar nuclei to form endosperm nucleus (triploid) to supply food during germination, the other male nucleus fuses with the ova NUCLEUS to form a diploid zygote
36
great stuff about asexual reproduction
rapid reproduction can produce large numbers of offspring does not need another organism/ plant