3 Flashcards

(97 cards)

1
Q

structure of egg cell

A

cytoplasm- where food reserves are found for developing embryo as it travels to the uterus lining
haploid nucleus
zona pellucida-protective coating that sperm have to penetrate for fertilisation to occur - hardens after fetilisation to prevent polyspermy
lipid droplets- food reserves for developing embryo
cell surface membrane
cortical granules-releases substances causing zona pellucida to harden to prevent polyspermy
corona rafiata-protective coating around the ovum
500um

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2
Q

structures of a sperm

A

acrsome- swells, fuses with sperm cell surface membrane and releases digestive enzymes that break down zona pellucida
flageluum- for movement
mitochondria- provide energy for movement of sperm
axoneme haploid nucleus 5um

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3
Q

process of fertilisation

A

sperm reaches ovum
binds to zona pellucida
chemicals are released from the cells surrounding the ovum, triggering the acrosome reaction
acrosome swells and fuses with sperm cell surface membrane
digestive enzymes in acrosome are released via excocytosis
enzymes digest through follicle cells and the zona pellucida
the sperm fuses with ovum membrane
sperm nucleus enters the ovum
corticual granules fuse with egg cell surface mebrane and enzymeses released from cortical granules through excocytosis thicken the zona pellucida preventing polyspermy and destory sperm binding sites
nuclei of ovum and sperm fuses

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4
Q

how do gametes form

A

meiosis producing gametes with 1/2 the number of chromosomes
chromosomes replicate before division, after replication each chromosme is made up of 2 strands of chromatiods, cell divides,.homologous chromosomes pair up then seperate, divide again producing 4 genetically different daughter cells

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5
Q

what is indpendent assortment

A

during meiosis only 1 chromosme from each pair ends up in the gametes. homologolus pairs line up at the equator in random order. The indpendent assortment of the chromosmes as they line up during meiosis is a source of genetic variation
as a result which chromosome of a given pair is pulled to which pole is indpendent to the behaviour of the other chromosmes in other homologous pairs
random process: either chromosomes from each pair could be in any gamete
produces genetically variable gametes

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6
Q

crossing over

A

during 1st meiotic division, homologous chromosmes come together as pairs and all 4 chromatids come into contact- at these contact points the chromatids break and rejoin, exchanging sections of DNA between non sister chromatids, point where chromatids break is called a chisma abd several occur along the length of each pair of chromosomes giving rise to a large amount of variation
crossover of non sister chromatid of homolgolus chromosomes ,break at crossover ( chiasma) & swap genetic information

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7
Q

linkage

A

one particular allele for a gene is inhereted with one particular allele for another gene
any two genes with a locus on the same chromosme are linked together and will tend to be passed as a pair to same gamete- linkage of genes
genes will only be seperated and go into different gametes if crossing over happens between the pairs of genes- if 2 genes very close to each other on the same chromosome, crossover is very unlikely to happen between them- strong linked
genes on a single chromosome make up a linkage group

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8
Q

autosmal linkage

A

two genes at similar loci on autosome and inherited as if they were the same gene

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9
Q

sex linkage

A

when locus of gene is located on sex chromosome , mostly in men
men only have one x chromosome
sex linked conditions: colourblindness, haemophilia

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10
Q

metaphase

A

spindle fibres forms and chromatids attach to spindle fibres by their centromeres
lined up on the equator of the spindle
chromosomes at this point are condensed as pairs of chroatid held together at the centromere

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11
Q

anaphase

A

spindle fibres shorten and pull the chromatids of each chromosme to opp sides of poles, splitting the centromeres
one chromarid of each chromosome is pulled to each poles
spindles break down

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12
Q

cytokinesis

A

in animal cells the cell surface membrane constricts around centre of the cell , a ring of protein filaments bound to the inside surface of the cell surface membrane contracts until cell divided
division of cytoplams to form seperate cells
cells appear to pinch at membrane called a cleavage furrow

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13
Q

purpose of mitosis- growth and repair

A

gentic stability achived by mitosis
genetically identical daughter cells
occurs in growth of any organism from single cell to multicellular
regenerate lost or damaged parts of body
if there is a wound cells can be replaced with the same cell type with same genetic quality

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14
Q

purpose of mitosis- asexual reproduction

A

reprodcution with no fusion of gametes
offspring genetically identical to parent
binary fusion- single celled organism divides by mitosis to form 2 daughter cells of equal size, both cytoplasm and nucleus / equally, bacteria + ameobas- not mitosis as no chromosomes
budding-new organism an outgrowth of parent, tiny duplicate of parent, nucleus / equally but cytoplasm unequally, yeast + hydra
vegetation propagation- part of the plant (root/stem/leaf) grows into a new genetically identical plant

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15
Q

telophase

A

2 new nuclei form at poles- chromosomes decondense , visible nuclear envelope
spindle fibres brokendown
each nucleus has a copy of every chromosme from parent cell
cell seperation begins
chromosomes unravel to become chromatin

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16
Q

prophase

A

by end of interphase the cell contains enough cytoplasm, organelles and DNA to form 2 new identical cells that are diploid
prophase: chromosomes condense becoming shorter and thicker with each chromosomes visible as two chromatids identical to each other if no mutation joined at centromere,centrioles move to opposie ends of the cell and produce spindle fibres to pull chromatids apart, nuclear membrane begins to breakdown

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17
Q

Stages of interphase

A

interphase: individual chromosomes are unravelled allowing acess to genetic material enabling new proteins to be synthesised
G1: cytoplasm volume increases by producing new proteins and cell organelles, in nucleus some genes are switched on and their base sequence to pre-mRNA
S phase: in nucleus there is replication of DNA, new histones synthesised and attach to replicated DNA in the nucleus, each chromosome becomes 2 chromatids attached at the centromere, growth of cell continues
G2: in nucleus replicated DNA double checked for errors and corrected if any errors found, if correction not possible cell cycle normally halted at G2 phase, cell growth continues by further synthesis of proteins and cell organelles

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18
Q

what does potency mean

A

the ability to divide and produce different types of daughter cells

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19
Q

stem cells

A

a cell that is undifferentiate but can conituosly divide to give produce specialised cells

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20
Q

what is a totipotent cell

A

a cell that has the ability to divide and differentiate into any type of cells

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21
Q

what is a pluripotent cell

A

a cell tht can divide to produce any cell (except placenta and umbilical cord in mamals)

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22
Q

what are adult stem cells used for

A

multipotent and found in bone marrow, liver, eyes and heart- raise less ethical concerns
bone marrow transplant- treatment of leukaemia
produce cells for transplantation- replace damged cells
production of blood vessels

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23
Q

embryonic stem cells

A

after uman zygote undergos 3 complete cell cycles it consists of 8 identical cells - each totipotent
after 5 days blastocyst formed which goes on to form placenta, inner cell mass of 50 cells goes on to form embryo- pluripotent

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24
Q

why are embryonic ste cellsbetter for treatemnt than adult stem cells

A

have the potential to develop into any cell type due to them being totipotent which offers the gratest flexibility for treatment, unlike adult stem cells which are committed to developing only into certain cell types

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25
what is a multipotent cell
can divide to replicte itself and produce different types of cells in one type of tissue - adult stem cells
26
ethical concerns with embryonic stem cells
-leftover embryos for IVF are 'living', 'killing unborn child' -can be seen as 'playing God'
27
descions society makes when using embryonic stem cells
stem cells are totipotent meaning they can be used in a wide range of therapies the source of embryonic stem cells has to be regulated ethical issues surrounding the destruction of embryos to obtain stem cells need for research establishment to be regulated
28
homologous pairs, sisg
homologous pairs have same genes but diff alleles
29
why offspring may be genetically different to each other
each zygote formed from different gametes- random fertilisation each gamete contains different combination of alleles this is due to indpendent assortment and crossing voer during meiosis
30
sex linked disorder
a mutation of a gene located on a x or y chromosme therefore disorder is more likely in one gender than another
31
why crossover may differ in sex chromosomes
conversion cannot occur between some sections of x and y chromosomes as not homologous pairs
32
Why gametes only receive one allele of each gene
In meiosis homologous chromosomes are separated from each other as well as spindle fibres pulling the sister chromatid apart to opposite ends of the cell so sister chromatid containing copies of the same cells separated from each other
33
why adult stem cells from one part of the body cannot be used in another part of the body
cells are not totipotent therefore some genes have already be acitavted and deactivated will not be able to specialise
34
how stem cells are used to replace damage cells
stem cells being {totipotent / pluripotent} ; continously divide to give rise to {differentiated / specialised} cells and these can replace damaged cells
35
how a fertilised egg can be used as a source of human pluripotent stem cells.
1. fertilised egg allowed to {grow for a few days/divide several times / eq} ; 2. reference to a {blastocyst/ blastula / hollow ball of cells / eq} ; 3. cells in inner cell mass are {pluripotent /harvested} ; 4. procedure for extraction of cells / eq ; 5. ref to source of fertilised egg e.g. spare embryo after IVF ;
36
sources of stem cells
1. cord blood /umbilical cord / placenta ; 2. {fertilised egg / zygote / eq} / blastocyst / (early) embryo ; 3. detail of site within blastocyst 4. bone marrow / eq ; 5. {brain / connective / skin / liver} cells / eq ; 6. addition of adult nucleus to enucleated egg cell
37
importance of meiosis in production of gametes
1. halves the chromosome number / eq ; 2. to produce a haploid nucleus / eq ; 3. so that at fertilisation the {fullcomplement / diploid number / eq} of chromosomes is restored / eq ; 4. allows genetic variation (in gametes) / eq 5. through independent assortment / eq ; 6. through crossing over / eq ;
38
why stem cells better used from patient and not another patient
1. cells have same genotype 2. no rejection / avoids immune response 3. idea of no disease transmission ;
39
similarities and difs of acrosome reaction and cortical reaction
both involve vesicles both involve the release of enzymes through exocytosis acrosome causes digestion of zona pellucida and cortical causes thickening of zona
40
how meiosis gives rise to genetic variation in gametes
independent assortment gives rise to different combinations of paternal and maternal chromosomes crossing over involves exchange of sections of non sister chromatid of homologous pairs resulting in new combinations of alleles
41
what is a locus
The position of a gene on a chromosome
42
why genes found in the sex chromosome pair have a pattern of inheritance different genes found on the other chromosome pairs
x chromosome carries genes not present on the y chromosome meaning males only have 1 allele of some genes and if only one allele then that allele will be expressed
43
what is the epigenome
DNA is wrapped around histone proteins and both the DNA anf histones have chem markers attached to their surface- make up the epigenome- influence the trancription of genes in the cell
44
effect methyl groups on DNA
attachment of methyl groups to DNA of a gene prevents transcription to mRNA by stopping RNA polymerase binding- winds DNA tighter
45
switched on and off
in cells of partocular type of tissue, all genes for specific funtion are active but all genses specific to other tissues are switched off During DNA replication the epigentic markers are copied so when a cell of a tissue divides if forms other cells with same fucntion
46
substrate hybridization
used to see acitve genes in specialised cells isolate mRNA from basic cell and specialised cell Reverse transcriptase transcribes specialised cell's mRNA to complementary DNA mRNA is digested before cDNA is hybridized with basic cell 's mRNA any mRNA that is alos produced in the differentiayed cell will combine with cDNA to form double strands- left over unpaird bases show acitve genes
47
what is an operon
group of genes under the same regulatory mechanisms and are all trancibed as a single unit found in groups of prokaryotic cells can turn specific genes on and off
48
bacteria lac operon
bacteria generally uses glucose as an energy source however when glucose is not avalibale bacteria can use lactose as an energy source but requires specific proteins produced by lactose operon
49
what is Lac I, promoter, operator Lac Z LacY
regulatory gene coding for repressor protein that prevents transcription of structural genes. Always turned on. section of DNA where RNAp olymerase binds to begin trancription section where repressor protein binds codes for B-galactosidase which catalyses hydrolysis of lactose to glucose and galactose. codes for membrane carrier protein lactose permease, which tensports lactose into bacterial cells
50
Lac operon when lactose not avalible
repressor protein binds to operator section preventing binding of RNA polymerase to the promoter region stopping tranciption of Lac operon- Lac Y and Z
51
expression of genes
stucture and function of each cell is depednent on the proteins it synthesises
52
effect acetyl groups on DNA
attach to histone and losen DNA making tranciprion easier
53
what happen to Lacoperon when lactose present
presence of lactose induces transcription of structural genes, allowing B-galactosidase a lactose permease lactose acts as inducer by binding to repressor protein or denaturing it. repressor protein is not able to bind to operator region RNA polymerase able to bird to promoter and begin transcription -lac operon is only expressed when inducer molecule is present to preserve energy.
54
what are adhesion molecules
recognition proteins one cell surface membrane that help cells recognise other cells like them and stick to them- extends from membrane and binds to complemnetary protenins on adjaxcent cells
55
organ
a group of tissues working together to carry out one function
56
phenotype
charecteristics of an organism which result from interaction of the genes of the organism and the environment
57
discontinuous variation
genetically determined and caused by monogenic inheritance where alleles are on the same locus has definite specific categories 2 or more categories with no intermediate values qualitative differences between phenotypes phenotypes that fall into discrete groups with no overlap
58
monohybrid inheritance
each locus is responsible for a different heritable feature
59
gene and environmental interactions effect on height
environment= diet genes for height but may not reach full potential due to malnutirtion
60
what switches transcription on and off in eukaryotes
genes is uncoiled regions of DNA can be transcribed into mRNA- RNA polymerase binds to a section ofDNA adjacent to the gnee-the promoter region gene remains switched off until enzyme attaches to promoter region- attachment of a regulatory protein usally required to start transcription transcription of a gene can be prevented by protein repressor molecules attaching to DNA of promotor region- blocking attachment site- can attach to regulatory protein preventing it from attaching
61
how a cell is specalised
•different stimuli activate different genes (chemical) •active genes are transcribed to mRNA °mRNA translated & produced to proteins for specific cell °proteins determine functions of cell °different genes activated result in different cell types
62
tissue
a group of specilaised cells working together to carry out one function
63
continuous varoation
no definite categories , continuous range of values ↳ quantitative differences between phenotypes presented as bell curve, most are at mean value a few at extremes affected by geneotype and environment - e.g. height- human can be any height within the human range controlled by genes at many loci - polygenic inheritance
64
multifactorial
conditions where several genetic factors and one or more environmental factors
65
melanin
made by cells called melanocytes activated by melanocytes stimulating hormone (MSH) binding to cell surface receptors which are triggered by UVA rays- melanocytes place melanin into organelles called melanosomes. melansomes are transferred to nearby skin and hair cells collecting around nucleus & protecting DNA from sun damage UV increases the amont of MSH and MSH receptors
66
master proteins
signal proteins- produced by the mRNA of master genes switch on the genes responsible for producing the proteins needed for specilaisation of cells in each segment
67
cause of cancer
occurs when the rate of cell multiplication is faster than rate of cell death- growth of a tumour caused by damage to DNA- can be reuslt of UV, radiation, asbestos, chems such as carcinogens, DNA mutation, abnormal methylation of genes in cancer cells can lead to activation or deactivation in genes involved in cell cycle
68
oncogenes
code 4 protein that stimulate the transition from 1 stage in the cell cycle to the next- dna mutation or epigenetic changes can lead to the cell cycle being continously activated
69
tumour supressor genes
produces supressor protein that stops the cell cycle- DNA mutation or epigenetic changes means there is no break in the cell cycle
70
Inherited cancer
faulty BRCA 7- gene predisposes individual to breast cancer ↳ produces protein repairing DNA ↳ makes individuals more susceptible to cancer
71
GR gene mice
GR gene (receptor protein binding to glucocorticoid) may be repressed by epigenome-due to poor grooming a ticking habits ↳ glucocorticoid is present in bloodstream causing increased anxiety levels in mice -GR gene is turned off if mother does not groom offspring , making lower GR stress receptors and high glucocorticoid levels
72
envirnomental causes of cancer
smoking- carcinogens in fags pose chemical risk , tar lodges in bronchi causes DNA damage surrounding epithelial cells -UV light: ionising radiation causes increased DNA mutation -low antioxidant diet : destroy cancer-causing fee radicals that damages DNA -Viral infection : hepatitis causes liver cancer ,HPV causes cervical cancer. Virus containsoncogene which interferes with cell cycle refutation
73
polygenic inheritance
a charecteristic showing continuos variation caused by multiple genes at different loci
74
decisions society makes about the use of embryonic stem cells
embryonic stem cells are totipotent and can be used in a wide range of therapies source of embryonic stem cells has to be regulated ethical issues due to the destruction of embryos to retrieve embryonic stem cells research establishment to be regulated
75
why adult stem cells from one tissue cannot be used to give rise to cells in another tissue
cells are not totipotent some genes have already been activated and deactivated will not be able to specialize into tissue cells
76
how epigenetic changes affect the activation of genes in daughter cells.
genes activated and deactivated by methylation and acetylation therefore same genes will be activated in daughter cell
77
why HCL is added in mitosis practica;
breaksdown middle lamella allowing cells to be seperated and producing a thin layer
78
why add a toluidine blue stain in mitosis practical
makes chromosomes visible so stages of mitosis can be identified
79
why people may be taller than their parents
height affected by environment as well as genotype as well as being polygenic inheritance therefore offspring can inherit a mixture of alleles from both parents that increases height. Environmental factors can be higher protein diet and better healthcare. Parents could of also not reached their genetic potential due to lower protein and calcium diet
80
how epigenetics affects body mass
DNA methylation deactivates genes affecting enzyme production and mtabolism
81
where to retrieve stem cells
bone marrow , blastocyst, skin, placenta
82
why there are regulating authorities for stem cells
decide on max age of embryo allowed for research setting or considering {ethical / legal} aspects / judging what is acceptable / follow acode of practice ; checking that source of stem cells is acceptable stopping of cloning (of humans) / eq ;
83
how offspring can be taller than biological parents
height affected by genotype and environment hieght proudct of polgenic inhertiance menaing a mixture of alleles from parents responisble for hieght environmntal factors- hugher protien diet and better helathcare
84
how transcription factors may cause somatic cells to be converted into iPS cells.
Transcription factors bind to promoter regions on DNA meaning no genes switched off as RNA polymerase now able bind to genes that were previously deactivated , mRNA produced and protein translated an folded. That allow cells to divide / undifferentiate /unspecialise as all genes are switched on
85
aseptic techniques when handling agar palte
working near a Bunsen burner to provide a convetion current • sterilising work surfaces • sterilising equipment with heat • limiting time containers are open
86
why agar palte is inucbated at 25 degrees
• to allow bacteria to multiply • without encouraging pathogenic organisms
87
sterilising techniques
boiling the culture medium before use { ‘flaming’ / disinfecting } of the instruments keeping lids off for the minimum time working in { updraught of a flame / a flow hood } disinfecting the bench (before or after working) autoclaving used plates
88
mitosis practical
C​ut a 5mm sample of the ​root tip​ using a ​scalpel​. Transfer root tip to sample tubes containing ​HCl​ and leave for 5 minutes-break up middle lamella creating a single layer of cells Transfer to watch glass containing cold distilled water. Leave for 5 minutes. Dry root tips on filter paper. Place tip on a microscope slide. ​Macerate​ with a needle to spread the cells out. This makes the chromosomes visible and will therefore show which cells are undergoing mitosis. Add a drop of ​toluidine blue​ to the slide and leave to stain for ​2 minutes​- taken up by sample- dying the cells so stages of mitosis can be viewed Lower the cover slip down carefully onto the slide. Make sure there are ​no air bubbles ​in the slide which may distort the image, and that the coverslip doesn’t slide sideways which could damage the chromosomes. Wrap in a paper towel and gently ‘squash’ the slide. Place under a microscope and set the ​objective lens​ ​on the lowest magnification, then use the ​coarse adjustment knob​ ​to move the lens down to just above the slide. Use the ​fine adjustment knob​ ​to carefully re-adjust the focus until the image is clear ​(can use a higher magnification if needed).
89
xylem+phloem practical
Calibrate the eyepiece graticule​ by placing both on the stage and lining up the divisions of the ​stage micrometer​ (which have a known length) with the divisions of the eyepiece graticule (for which the length is unknown) to calculate the length of one division of the graticule. Cut ​transverse​ sections of the plant stem (on the white tile using a razor, wet to reduce friction) as thinly as possible. Select the thinnest sections. Place one section on a microscope slide. Draw a ​line in wax crayon​ from top to bottom of the slide either side of the specimen to prevent the dye from spreading. Add a few drops of ​concentrated phloroglucinol​ and lower the cover slip down carefully onto the slide. Make sure there are ​no air bubbles​ ​in the slide which may distort the image. Place under a microscope and set the ​objective lens​ ​on the lowest magnification, then use the ​coarse adjustment knob​ ​to move the lens down to just above the slide. Use the ​fine adjustment knob​ ​to carefully re-adjust the focus until the image is clear (can use a higher magnification if needed). Observe and draw the stem. Measure the size of the ​stem diameter​ and ​vascular bundle​ using the calibrated eyepiece graticule
90
controls for plant fibre practical
length and width of each fibre should be around the same length for even comparison, the mass used for each fibre should be the same.
91
fibres experiment
Cut all the fibres to the same length and width Attach each end of the fibre to a clamp stand and add masses in the middle. Continue until the fibre snaps and record the mass with which the fibre snaps. Repeat with all fibres force/cross sectional area of fibre= tensil strength- micrometre and eye piece gratica to measure width
92
aseptic techniques
Surfaces should be wiped down with an antibacterial cleaner before and after the experiment Keep the Petri dish close to the Bunsen burner so convection currents draw microbes away from the culture Flame the neck of any bottles to prevent bacteria entering the vessel and flame equipment to sterilise Keep all vessels containing bacteria open for the minimum amount of time. Keep all windows and doors closed to limit air currents.
93
controls of antimicobrial practical
Same concentration of plant material used Type and amount of bacteria used – E.coli will be used as the bacteria and it will be evenly spread across an agar medium Volume of plant material used for each disc – 0.1 cm³ can be used per sterile paper disc each time Contamination of culture – aseptic techniques and sterile equipment used to avoid contamination of bacteria culture Temperature of cultures – all Petri dishes should be incubated overnight at the same temperature pH of medium – an agar jelly will be used in each case with a consistent, neutral pH
94
antimicrobes practical
Crush 3 g of garlic with a pestle & mortar and use a measuring cylinder to add 10 cm³ of denatured alcohol to the mixture. Shake the mixture occasionally for 10 minutes. Repeat step 1 but this time using 3g of the mint plant material. Pipette 0.1 cm³ of the garlic extract solution onto 4 of the sterile paper discs. Allow each disc to dry. Repeat this process for the mint extract solution. Label the other Petri dishes for garlic, mint and control solutions – include the date. Use the sterile forceps to place all 4 discs of each type of extract onto their corresponding Petri dish. Close each dish and seal with hazard tape. Make sure that a small gap is left so that oxygen can enter and there is no build-up of anaerobic bacteria.Leave the cultures to incubate overnight. Open each Petri dish and use a ruler to work out the zone of inhibition for each paper disc.
95
serial diultion
reduces conc of substance, antimicorbiral pectaical to determine most effective concentration
96
how dna mutation could increase rate of division of stem cells
{mutation / change in base sequence} of a gene for {check point protein / cell cycle (control) protein} (1) no check point (1) activating oncogenes / deactivating tumour suppressor genes (1) cell {cycle / division} is no longer inhibited / shortening the cell cycle
97
how twin studies show nature and nurture effects
1. { identical / monozygotic twins } are genetically identical / eq ; 2. derived from one egg and one sperm /one { zygote / embryo / eq } / eq ; 3. (so any phenotypic ) difference is due to { nurture / environmental } / eq ; 4. {non-identical twins / dizygotic twins} are genetically different ; 5. (any phenotype) that is different when the environment is the same is likely to be { nature / genetic / eq }