topic 6.2.1: cloning and biotechnology Flashcards
what is vegetative propagation
asexual reproduction using meristem cells from vegetative organs eg roots and shoots tips, vascular cambium
what are runners
horizontal stems that point away from the plant so new clones can grow
what are rhizomes
underground runners
how are plant cuttings grown
cut off none flowering stems, dip in plant hormones and fungicide, grow in soil
what is micropropagation
multiplies plants from small pieces of tissue grown in sterile environment, producing cloned plantlets
are plant cells pluri or totipotent
toti
how would you micropropagate a plant
take tissue culture, sterilise with ethanol, grow with hormones, callus forms and splits into cells, transfer to agar
advantages of micropropagation
rapid, disease free, can clone gm or seedless plants
disadvantages of micropropagation
expensive, requires skill, reduced gene pool, susceptible to same diseases
how are animals naturally cloned
monozygotic twins
embryo splitting
two desirable parents selected, female given hormones to produce many eggs, ivf, egg splits, cells inserted into surrogates
somatic cell nuclear transfer
somatic cell taken from body, eggs cell enucleated, somatic nucleus inserted, electrical current stimulates division, embryos inserted into surrogates
what type of clones does embryo splitting produce
each other, not parents
what type of clones does somatic cell nuclear transfer produce
each other and parents
advantages of artificial cloning of animals
more offspring, cloning of gm animals, protect endangered species
disadvantages of artificial cloning of animals
inefficient, high miscarriage rate, shorter lifespan
advantages of microorganisms of biotech
economic advantages, basic growth requirements, faster food production due to short lifecycle
advantages of microorganisms of biotech
microbes grow rapidly, can be gm, no ethical concerns, healthy
disadvantages of microorganisms of biotech
can produce toxins, aseptic, not appealing, needs additives
how are microorganisms cultured
pour sterile agar in to petri dish, flame neck of culture, take sample with sterile inoculating loop, flame neck, replace plug, wipe end of loop on agar, tape lid and incubate at 25 degrees for 24hours
batch fermentation
all nutrients added and then allowed to grow until desired product obtained
manipulating conditions impacts growth, metabolism etc
continuous fermantation
continuous flow of sterile medium while removing equal products
number of individual organisms =
initial number x number of divisions
phases of standard growth curve
lag, exponential, stationary, death
4 methods of immobilising enzymes
adsorption, covalent bonding, entrapment, encapsulation
advantages of immobilised enzymes
don’t need to purify, can be reused, decreased sensitivity
advantages and disadvantages of adsorption
simple, cheap, versatile
enzyme may detach, surface could cover as
advantages and disadvantages of covalent bonding
strong, readily in contact
varied cost, bonding could change tertiary structure
advantages and disadvantages of entrapment
versatile
expensive and time consuming