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240 Cards in this Set

  • Front
  • Back

which monosaccharides make MALTOSE

glucose + glucose

which monosaccharides make LACTOSE

glucose + galactose

which monosaccharides make SUCROSE

glucose + fructose

what kind of sugar is glucose

hexose sugar

monosaccharides join to make disaccharides and polysaccharides with what bonds

glycocidic bonds

name test for sugars

benedicts test

method of testing for sugars

1) add benedicts reagent


2) heat to boil


3) +ve is red


if negative


4) add HCL to break poly to mono


5) boil


6) add NaOH to neutralise


7) do benedicts test again

name 3 polysaccharides

starch


glycogen


cellulose

what is starch

plans excess glucose storage

what reaction breaks polysaccharides

hydrolysis

what reaction makes polysaccharides

condensation

what is the test for starch called

iodine test

how do you test for starch

add idodine dissolved in potassium iodide


+ve change from orange/brown to blue/black

what is glycogen

excess glucose storage in animals


has many side braches to can be released quickly


not common- main energy storage is fats

what is cellulose

long unbranched chain of beta glucose


straight chains


linked by hydrogen bonds to form microfibrils


stuctural support

monosaccharide + monosaccharide =

disaccharide

disaccharide + monosaccharide =

polysaccharide

what is a triglyceride

one glycerol with 3 fatty acids attached


structure of fatty acid tails vary

how are triglycerides formed and what bond

condensation reaction


esther bond

what makes triglycerides saturated/undaturated

fatty acid tail


saturated- no double bond


unsaturated- one or more double bonds

what is a fatty acid tail

hydrocarbon chain


hydrophobic

what makes lipids insoluble

hydrophobic hydrocarbon/fatty acid tail

what is a phospholipid

glycerol with two fatty acids and a phosphate group attached

where are phospholipids found and why

cell membranes


phosphate head is hydrophilic and fatty acid tail is hydrophobic so form a phospholipid bilayer

name the test for lipids

emulsion test

how do you test for lipids

1) add ethanol


2) pour into water


3) +ve is a milky emulsion


4) more lipid- more emulsion

use of lipids other than membrabe and why

source of energy


fatty acid tails contain many bonds so lots of energy is released when they are broken


so contain more energy than carbohydrates per gram

lipids are insoluble why is this useful

dont affect water potential and cause cells to burst via osmosis

what are lipids soluble in

inorganic solvents

how many types of fatty acid are there

70

amino acid + amino acid =

dipeptide

dipeptide + amini acid =

polypeptide

structure of amino acid

amine group (NH2), carboxyl group (COOH), lone hydrogen and an R group/ residual side group

describe primary protien structure

sequence of amino acids in a polypeptide chain

describe secondary structure of a protien

hydrogen bonds, polypeptide chain coils into an alpha helix/beta pleated sheet

describe tertiary structure of proteins

hydrogen bonds


ionic bonds


disulphide bridges


form a more coiled 3D structure/globular protein

describe a quartinery structure of a protein

multiple chains held together by all bonds in tertiary

4 protein uses

enzymes


antibodies


transport protiens


structural/channel proteins

name test for proteins

biuret test

how do you test for proteins

1) add NaOH


2) add CuSO4 solution


3) +ve goes purple,-ve stays blue

what are enzymes

proteins which are biological catalyst that lower the activation energy of a reaction


theyvcan be intra/exra cellular


have specific active site due to tertiary structure which substrate binds to to form an enzyme substrate complex

what do enzymes do to substrates and how

1) join two by holding them close and reducing repulsion so they can bond easily


2) break into two substrates as active site causes strain on bond so breaks easily

describe induced fit model

substrate has to be right shape and make active site right shape when enzyme substrate complex forms

describe the lock and key model

substrate and actuve site right fit

list properties of enzymes

specific and catalyse one reaction


different tertiary structure means different active site


tertiary structure is altered be changes in temp, pH, etc

how do mutations affect enzyme production

primary structure determined by gene


if mutation in gene


could change tertiary structure of enzyme produced

describe effect of temp on enzyme activity

rise makes more vibrations


so more collisions


more enzyme substrate complexes


so faster rate of reaction


if abouve certain temp enzymes denature because tertiary structure changes shape


so active site changes shape


so substrate wont fit

describe the effect of pH on enzyme activity

most work best at 7


pepsin works best at 2 because it is found in the stomach


abouve and below optimum pH OH- and H+ ions mess up ionic and hydrogen bonds changing tertiary structure


changing active site


denatured

dedcribe effect of enzyme concentration

more enzyme means faster ror until more enzyme than substrate so levels off

describe substrate concentration effects

more substrate means more collisions


until saturation where all enzyme active sites are full then levels off

what is competitive inhibition

inhibitor same shape as substrate so fits in active site but no reaction so no substrate can fit in


more inhibitor means less enzyme substrate complex


more substrate means more enzyme substrate complexes

what is non competitive inhibition

inhibitor binds to side of enzyme


causes active site to change shape


substrate cant bind


increasing substrate has no effect

how do you calculate rate of reaction

tangent then gradient

what is a nucleotide

nitrogen containing organic base


with pentose sugar


and phosphate group

list 5 bases

adenine


guanine


cytosine


thymine


uracil

A pairs with? and how many hydrogen bonds

Thymine in DNA


uracil in RNA


2 bonds

guanine pairs with? and how many hydrogen bonds

cytosine


3 bonds

nucleotides join to form ? which joins pentose sugar and phosphate with what bonds to form what

polynucleotides


phosphodiesther bonds


sugar phosphate back bone

describe DNA structure

double helix with gydrogen bonds between bases


complimentary base pairing


two strands run anti parallel


3 prime and 5 prime

describe structure and types of RNA

single chain


mRNA made in transcription, carries code to ribosomes


tRNA used in translation, carries amino acids to ribosomes

who discovered DNA and when

watson and crick


1953

describe DNA function and why

pass on genetic information


stable and rarely mutates


2 strands can seperate for DNA replication


large molecule so more information

how does DNA replicate

semi conservative replication

when does DNA replicate

before cell division

which enzyme seperates the strand of DNA and what bonds does it break

DNA helicase


hydrogen bonds

describe DNA replication

strands unwind


act as a template


free floating DNA nucleotides are attracted to the two strands and complimentary base pairing takes place


condensation reactions with DNA polymerase join the nucleotides


2 new strands contain one original and one new

what is conservative replication

two old strands would stay together

who proved the semiconservative replication

meselson and stahl

hiw did they prove smeicinsevative replication

N15 and N14


initial DNA containing N14 settles at top of tube


N15 replicates in N14 broth


then centrifuge


semi meant 1 line in middle


conservative would be 2

water use

metabolite


solvent


temp control


cohesive so transport

describe structure of water

H2O


polar


H+ O-

high latent heat of vapourisation

lots of energy to break bonds


so lots of energy is used to evaporate it


useful as cools when sweating

water buffer

hydrogen bonds absorb energy


so hight specifuc heat capacity


so water doesnt have rapid tem changes so maintains constant body temp

water as a solvent

things can dissolve in it


like inoganic ions

water is cohesive

helps flow


good gor transporting


high surface tension

what is ATP

a phosphorilated molecule


adenine base with ribose sugar and 3 phosphate groups

what is ADP

adenine


ribose


2 phospate


hydrolysis from ATP

AMP?

adenine


ribose


1 phospate

adenosine

adenine


ribose

when does ADP to ATP occur

1) chlorophyll- photophsophrilation


2) respiration in plant and animal cells- oxidative phosphoylation


3) in plant and animal cells when phosphate groups are transferred from donor molecules- substrate level phoshorylation

how does ATP work

energy released when phosphate broken off in hydrolysis


fast


catalysed by ATP hydrolase

ATP formation

catalysed by ATP synthase


phosphate ion and ADP


fast

use of FE2+ ions

haemoglobin


4 polypeptide chains with one fe each


o2 makes fe3+ for a bit

use of H+ ions

more h+ lower ph

Na+ ion use

cotransport of glucose and amino acids

use of PO4 3- ions

ATP


DNA


RNA

eukaryotic cells

animal and plant


nucleus


cell surface membrane


ER

prokaryotic

circular DNA


bacterium


slime capsule

plant cell

celulose cell wall


vacuole


chloroplasts

algal and fungal cells

like plant cells


fungal have chitin cell wall and no chloroplasts

cell surface membrane

made of lipids and protein


regulates movement of substances


receptor molecules

nucleus

nuclear envelope


pores


protein bound DNA


nucleolus


conrol cell activity


instructions for proteins


makes ribosomes

mitochondrion

double membrane


inner folded into cristae


filled with matrix


contains enzymes for respiration


site of areobic respiration


active so more energy

chloroplast

double membrane


thykaloids- stacked up form grana linked by lamellae


photosynthesis takes place

golgi

fluid filled sacs


vesicles at edge of sacs


processes and packages lipids and proteins


makes lysosomes

vesicle

stores lipids and protiens


takes out of cell

lysosome

no structure


contains lysozymes


digestive enzymes

ribosome

protein synthesis

ER

rough- ribosomes


folds and processes proteins


smooth- lipids

cell wall

made of cellulose


support

vacuole

cell sap


membrane called tonoplast


maintain pressure

prokaryotic structure

no membrane bound organelles


plasma membrane


cell wall


capsule


palsmids loop of DNA


circular DNA

virus

a cellular


nucleic acid surrounded by proteins


invade and reproduce


protein capsid


attatchment proteins

binary fission

DNA replicates


move to poles


divides to 2 identical daughter cells

virus replication

host cell by attatchment proteins


virus to only one type of cell

light microscopes

light to form image


0.2 micrometres

electron microscopes

higher resolution


0.0002 micrometres

transmission microscope

electro magnets


see internal structure


only thin specimens

scanning microsocpe

electron beam


3D surface only


thick specimines


lower res

cell fractionation

homoginisation


filtration


ultracentrifugation

mitosis

pmat

interphase

cell normal functions


DNA doubles

prophase

chromosomes condense


visable


centrioles move to opposite ends of cell form spindle fibres


nuclear envelope breaks down

metaphase

chromosomes line up along equator


become attatched to fibres

anaphase

centromeres divide


seperating chromatid pairs


spindles vontract bringing chromatid to poles

telophase

uncoil to thin and invisible


nuclear envelope forms 2 nuclei


cytopladm splits


2 identical daughter cells

cancer

uncontrolled cell division

mitotic index

chromosomes÷total

artefact

dust etc

fluid mosaic structure

bilayer is fluid


has cholesterol


proteins- channel and carrier allow large molecules


receptor proteins react to hormones


lipids have polysaccharide chain called glycolipids

cholesterol use

makes membrane more ridgid


maintain shape

diffusion

net movement from high to low conc


passive

facilitated diffusion

carrier protiens


large molecules


passive

osmosis

diffusion of water from high to low water potential

isotionic

sam ewater potential

when % change in mass is 0

water potential of sucrose is same at potato

active transport

active uses ATP


agains conc gradient

co transport

2 molecules at same time


conc gradient of one is used to move the other against its own

glucose enters ileum with

sodium

phagocytosis

foreighn or non self antigen trigger immune response


1) phagocytes engulf


2)recognises non self


3)pathogen engulfed and contained 4)in phagocitic vacuole


5)lysozymes break down


6)phagocye presents pathogen antibodies for lymphocytes to detect

t cells

activated by phagocytes


receptor proteins bind to complementary antigens


t helper- release chmeical signals to activate phagocytes and t killers an b cells


t killers- kill abnormal cells eg infected body cells

b cells

covered in antibodies bind to antigens


clonal selection


divides into plasma cells

plasma cells

make antibodies


monoclonal antibodies

antibody

2 binding sites


specific


proteins


2 light chains


2 heavy


joined by disulphid bridges

aglutination

antibodies clump to several antigens at a time and surround pathogen marker for phagocyte

immune response

cellular


t cells etc


humoral


b cells clonial selection


antibody production

primary response

antigen activates immune system


slow not many b cells


after exposure t and b memory cells produced


remain in the body


immune

secondary immune response

same pathogen


quick response dues to memory cells

vaccine

dead or inactive antigens


with out cauding disease

herd immunity

mass immunity


less people to catch from

antigenuc variation

pathogens can change shape of antigens by random mutation so not triggering memory cells

passive immunity

natural baby milk from mother


arteficial antibody injection

active immunity

natural immune after catching


arteficial immune after vaccine

cabcer treatment with monoclonal antibodies

attatch drug to antibody


antibody attatch to mutated cell

pregnancy testing

detect hcg found in pregnant women


antibodies attatched to blue bead


urine carries beads due to antigen antibody complex


strip turns blue

elisa

see if patient has certain antibodies


1) hiv antigen to bottom of well plate


2) sample added and wash


3) hiv antibodies will bind


4) seconary antibody added


5) wash


6) add substrate with colour


7) if present will be colour change

hiv

core contains genetic material


protein capsid


envelope made of stolen membrane


attatchment proteins attatch to t helper

hiv replication

attatch to receptor


capsid release RNA


make dna fron the rna


dna inserted into human dna


viral proteins assembeled and sent out

counter current flow

water enters


gill fillaments with lamellae with capilaries large sa


blood flow in one direction water in opposite


maintains diffusion gradient

insects

air moves into trachea through surface pores called spiracles


O2 travels along conc gradient to cells


CO2 moves back to spiracles

dictotyledonus plants

main gas exchange is mesophyll cells on leaf surface


gas moves in and out via stomata pores


guard cells controll opening of stomata

control water loss

insects- waxy coating close spiracles tiny hairs around them


plants- stoma open in day


water enters guard cell making them turgid opening the stomata for water loss

gas exchange in humans

trachea


bronchi


bronchles


alveoli

inspriration

inter corstal muscles contract


increase volume air pulled in

expiration

muscles relax


air forced out

lung disease

tb-damages gas exchange surface


fibrosis- scar tissue


asthma- inflammation


emphysema- inflammation attracts phagocytes break down elastin

carbohydrates broken down by what

amalayse


produced in slaivary glands

lipid broken down by what

lipase


produced in pancreas


eork in small intestine


lipd and bile salts produced in liver emulsify


lipid broken down and fatty acids stick with bile salts to form micelles

protein break down

endopeptides


within protein


pepsin


exopeptides


at ends


remove single amino acids


cell surface membrane

micelles function

move monoglycerides to epithilium

heamoglobin

quartinery structure protien


4 chains with heam group wit hfe ion attatched

partial pressure of oxygen

measure of oxygen concentration

raise in CO2

low affinity for oxygen

vein to kidneys

renal vein

arteries

from heart


thick muscle


elastic tissue to recoil maintain high pressure


folded inner lining to stretch

vein

to heart


low pressure


little elastic muscle


valves prevent back flow


thick muscle

capillaries

one cell thik


good diffusion

tissue fluid

hydrostatic pressure high than in fluid near arteries


forces fluid out


reduce pressure so lower at end of capillary bed


so lower water potential


so fluid reenters


some fluid drained to lymphatic system

heart

pulmonry artery aorta


vena cava pulonary vein


right atrium left atrium


semi lunar valves


atrioventricular valves


right ventricle left ventricle

heart properties

left more muscle powerful pump blood out


ventricles thicker have to push blood out


av valves stop back flow to atria


sl valves stop back flow to heart


chords stop valves being forced open

atheroma

damage to artery


white blood cells clump and lipids


fiborous plaque forms

aneurysm

increase blood pressure due to atheroma


form sac


burst sac

thrombis

plaque rupture


damage artey


blood clots

high chloesterol

reafily for atheromas


high salt high blood pressure

nicotine

high bp

xylem

water and mineral ions


long


no end walls


formed from dead cells

chesion and tension

water moves up plants


1)evaporate at top


2) tension/suction so water forced up tube


3) cohesive so pull each other up


4) water enters roots

transpiration

water evaporates and acumilates at leaf


stomata open


water moves down leaf conc gradient and out

phloem

organic substances


sieve tubes living cells that form tube have few organelles so there are


companion cell for each sieve tube element provide energy for active transport


translocation

movement of solutes


active


move from sources to sinks made to used


enzymes maintain conc gradient at sink by breaking down/converting the solute that arrives

mass flow hypothesis

active transport


lowers water potential in sieve tubes so osmosis from xylem


high pressure at source


at sink solutes are removed increasing water potential


osmosis to xylem


lowers pressure


pressure gradient moves solutes to sink

linear DNA

long so has to be wound up


wound around proteins-histones


help support DNA


coiled tightly to make a compact chromosome

super coiling

DNA compaction in circular DNA

genome

complete set of genes in the cell

proteome

full range of proteins cell can produce

intron

doesnt code for amino acids

exon

codes for amino acids

allele

different form of a gene

mRNA

has codeons


codes for maino acids at ribosome

tRNA

hydrogen bonds between pairs hold its shape


carries an amino acid and an anti codon

transcription

mRNA copy made


RNA polymerase unzips DNA


used as template


t replaced by u


when RNA polymerase reaches stop triplet it detatches and mRNA stops being made

transcription pt 2

introns and exons are copied into mRNA so splicing occurs


leaving exons


mRNA leaves the nucleus

translation

mRNA attatches to ribosome


tRNA carry amino acids to it


ATP provides energy for bond to form


tRNA anticodon complimentary to mRNA codeon attatches to mRNA


second pair do the same


amino acids are then joined by peptide bond


tRNA molecules move away


makes chain until stop codeon

genetic code

non overlapping base used once


degenerate more combinations tgan amino acids so some code for same


universal same triplets code for the amino acid in all living things

gametes

sex cell passes DNA down


haploid

meiosis

gametes made


dna replicates


double armed chromosomes made from 2 sister chromatids joined by centromere


homologous pairs line up crossing over takes place


sperated halving chromosome number


chromatids are seperated centromere divided


4 haploid genetically different cells are made

independant segrigation

random seperation of the mother father homologous pairs


so random which chromatids end ul with which

chromosome mutation cause

error in cell division

substitution

one base for another


not always a problem


due to degenerate code

deletion

one base deleted


every triplet after has changed so completely different amino acids

mutagenic agents

radiation


chemicals


viruses

genetic diversity inceased by

lots of alleles


mutation

genetic bottle neck

most of population dies


smaller gene pool

behavioural adaptation

actions

psychological adaptaion

processes in body that increase chance of survival

anatomical adaptation

structural features of body

directional selection

characteristics of and extreme are more likely to survive

stabilising selection

middle of range more likely to survive

aseptic techniques

disinfect


near bunsen


sterilise loop


flame bottle neck

phylogeny

evolutionary history of organisms

taxonimy

classification

classification list

domain


kingdom


phylum


class


order


family


genus


species


digest king prawn curry or fat greasy sausages

binomial naming system

genus, species

gonome sequencing

dna sequence can be determined


and compared


amino acid sequence comparison

similar dna means similar amino acid sequence

immunological comparisons

similar proteins will bind to similar antibodies

biodiversity

variety of different organisms in an area

habitat

where organism lives

community

all populations of different species in a habitat

species richness

number of species in an community

monoclonal antibodies

produces from single group of same b cells


identical


can bind to anything


eg to cancer cells


which have tumor markers


so make monoclonal antibodies attatch to those


few side affects

ethical issues of vaccination

animal testing


human testing can result in altercations


risk of side effects

hiv causes aids how

deteriorates the immune system by targeting t helper cells


antibiotics dont work on viruses?

interfere with metaboluc reactions of bacteria by targeting the ribosomes and enzymes


this is because those bacteria and enzymes are different to that of a humans


viruses use host cells ribosomes and enzymes making them uninhibitable by antibiotics


smaller animals have a ...... sa:v

higher

rate of heat loss is affected by

size

tidal volume

volume of air in each breath


0.4-0.5 dm3

ventilation rate

number of breaths per min


15ish

forced expiratory volume

max air breathed out in 1 sec

forced vital capacity

max air to be forcefully breathed out of the lungs after a really deep breath in

spiriometer

used to wok out tidal wave etc

monoglyceride

glycerol with one fatty acid

vena cava

deoxygenated to the heart from body

pulmonry artery

deoxygenated to lungs from heart

pulmonry vein

oxygenated from lungs to heart

aorta

oxygenated to body from heart

cardiac cycle

diastole


atrial systole


ventricular systole

diastole

blood into atria


high pressure


atrioventricular valves open


all walls relaxed


semi lunar valves close due to pressure change

atrial systole

artia contract


ventricles relax


small volume incresed pressure in atrias


blood pushed into ventricles

ventricular systole

atria relax


ventricles contract


atrioventricular valves close


semi lunar valves open


blood to arteries