molecular genetics Flashcards
DNA (6)
- anti-parallel strands
- genetic material in living org
- store genetic info control characteristics
- inherited from parents
- double helix structure, found in nucleus of cell
- transmitted to nxt gen
What is genetic engineering?
technique used to transfer genes from one org to another. indiv genes may b cut off from the cells of one organism & inserted into the cells of another org of the same or diff species. transferred gene can express itself in the recipient organism.
what is required for gene transfer?
a vector(usually a plasmid)
what is a vector
- another DNA molecule
- a bacterium
- virus
used to carry the genes of one organism into another. small circular DNA called plasmid, obtained from bacterium can b used to transfer genes
what is a transgenic organism?
one that has acquired a foreign gene(not found in the organism)
step 1 of production of insulin by bacteria using genetic engineering(hint: cutcut cucumber, and what does it produce?)
Isolation of insulin gene:
- use restriction enzyme(like scissors) to ‘cut’ the insulin gene from the human DNA by breaking the bonds between the bases
- produces a DNA fragment containing the insulin gene w sticky ends on both sides->(means thy can join to another single-stranded gene later)
- each sticky end is a single strand of DNA bases -> can pair w complementary bases to form a double strand
(the 2 sticky ends r gna b complementary bcos the enzyme only cuts a specific base pattern)
step 2 of production of insulin by bacteria using genetic engineering(hint: keep cutting don’t stop cutting, specify cut with what?)
Isolation of plasmid DNA frm bascterial cell:
- plasmid DNA is isolated from the bacterial cell
- using the same restriction enzyme, the plasmid DNA is cut to produce a linear strand of plasmid DNA w complementary sticky ends(bcos u use same restriction enzyme)
step 3 of production of insulin by bacteria using genetic engineering(hint: ur making a salad, aft cutting all the vegas, u put them in a bowl and ?)
Insertion of insulin gene into the plasmid DNA:
- the DNA fragment w the insulin gene is MIXED w the cut plasmid DNA
- enzyme DNA ligase is used to seal/join the insulin gene to the plasmid by catalysing the formation of bonds btwn the complimentary bases
step 4 of production of insulin by bacteria using genetic engineering(hint: what is a way to give death sentence/ torture method)
Introduce the (recombinant) plasmid carrying the insulin gene into the bacterial cell:
- mix the recombinant plasmid w the bacteria(E.Coli)
- apply temporary heat or electric shock to open up the pores on the cell membrane of the bacteria for plasmid to enter
- thus plasmid acts as a vector(carrier/vehicle) to carry the insulin gene into the bacterium
- once this is successful, the bacterium will multiply and all the bacteria produced will hv the human insulin gene in them
- each bacterial cell will start to make insulin molecule
how to extract the insulin frm the bacteria?
kill the bacteria and burst it so tht all of the insulin will cm out which has to b purified b4 it can b used
concerns of the previous way of obtaining insulin?(5)
- disease(MERs, SARs. Covid-19) that may not be fatal to animals but could be to use due to cross-breeding
- very inefficient
-development of allergies against it aft a prolonged use - many diabetics develop antibodies against animal insulin aft prolonged treatment: hv to take immuno-suppressive drugs to suppress the immune system so thyll b more vulnerable to diseases–>
become more susceptible to diseases
advanatages of insulin produced by genetic engineering(5)
exactly same as ordinary human insulin, so:
- does not induce allergic response in the patients as the insulin produced is identical to human inculin
- easier and cheaper to produce insulin(since it is produced in a short time n in large quantities compared to when extracted from animals)
- less risk of contamination by disease-causing microorganisms like bacteria as compared to insulin obtained from the increases of animals
- body will not develop antibodies against it–> patients does not need to use immuno-suppresive drugs to suppress immune system
- ethical concerns of vegetarians or religious grps can b overcomes since vegetarians may object to the use of insulin obtained from slaughtered animals
DNA winds around…
proteins to form chromatin
chromatin winds around…
itself during cell division to form chromosome (in nucleus of every cell)
each DNA strand has
- 2 parallel poly nucleotide chains that run in opp direction (anti parallel) twisted to form the double helix
- sugar phosphate backbone
- sides made up of sugar and phosphate molecules
- rungs made up of base pairs (ATCG)
complementary base pairing
- Adenine pair with Thyamine/Uracil
- Cytosine pair with Guanine
gene (4)
- basic unit of inheritance
- sequence of nucleotide that determines formation of a single polypeptide (simpler ver of protein) which is used to make protein, codes for polypeptide when expressed
- 2 polynucleotide chain but only one determines type of protein made ( junk gene)
- stores info for a specific type of protein
type of protein produced controls…
… characteristic and behaviour of cell
- determines traits/ observable features
protein –> ribosome –> outside nucleus –> modified in golgi apparatus
protein synthesis methods
transcription and translation
transcription (whr, what, how)
- nucleus
- process whr DNA template is copied into single stranded messenger RNA
only 1 side has genetic codes, other side is junk so…
- DNA unwinds and unzips
- mRNA molecule copies genetic code in DNA template
- following the rule of complementary base pairing but A pairs with U instead
translation (whr, what, how)
- in cytoplasm
- whr sequence of mRNA codons is used to make polypeptides
- every 3 nucleotide = 1 amino acid
- AUG –> start codon
- UAG, UAA, UGA –> stop codon
- mRNA attaches to a ribosome that moves along mRNA and translated the msg into a sequence of aa joined 2gt forming polypep
- tRNA brings aa to ribosome (transfer RNA)
- as ribo moves along, polypep gets longer
- at end of mRNA strand, ribo detaches, polypep released
how is insulin commerically produced?
the recombinat bacterium can b isolated & cultured in large sterile containers called fermentors to produce human insulin on large scale, under optimum conditions(o2 conc, pH, temp&; conc of nutrients–> carefully monitored by a computer), when a large population of bacteria is produced–> removed from the fermenter and insulin is extracted from them–> it is then purified, tested and packaged and sold
benefits of GE (4) - plants + meds + rice
- prod crops that can grow under extreme conditions(eg, droght-resistant crops, salt-tolerant crops, crops that make more efficient use of nutrients)–> allows farmers to grow crops even when the envo conditions is not suitable 4 cultivation most crops
- development of pesticide resistant crops + crops that produce toxins that kill insects: the use of costly pesticides that may damage the envo is reduced
- low cost prod of medicine–> ge of impt drugs such as human insulin has drastically reduced the cost of these medicines, w these drugs becoming more affordable, more patients can get access to them and be treated
- improved nutritional quality–> golden rice–> high vitaminA content
risks of GE (3)
- ppl allergic to transgenic food (lectin that deters aphids from feeding may be transferred to the potato plant)
- genes coding fot antibiotic resistance may accidentally be incorporated into bacteria –> diseases in humans
- deliberate abuse bio warfare, designer babies :((