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bacterial chromosome
1 double-stranded circular DNA molecules + associated proteins
plasmids: small circular pieces of DNA (exist & replicate independent of bacterial chromosome)
not required but give benefits
reproduction in bacteria
reproduce by binary fission (asexual) — produce genetic clones
mutation = source of variation
mechanism of gene transfer/recombination in bacteria
transformation
conjugation
transduction
transformation
when small pieces of DNA are taken up by the bacterium from its surrounding environment
can be from free DNA piece or plasmid
free can be incorperated into bacterial chromosome
plasmid can operate independently or incorporated
biotech link with transformation
genes of interest are splice using restriction enzymes & the bacterial cells can me “made” to take up the plasmid (competency)
how to make bacterial cells competent
heat shock: quickly change temp of bacteria’s environment
altering calcium ion concentration
electrical impulses
conjugated (bacterial sex)
unidirectional transfer of genetic material between 2 bacterial cells
male has pili (protein-hair like extensions) that attach to female
they join & DNA is passed from male to female
what determines bacteria’s ability to form pili
f-factor (fertility factor) — codes for production of sex pili — can be found on bacterial chromosome or plasmid (f plasmid)
biotechnology link with conjugation
specific plasmid is r plasmid (antibiotic resistance)
antibiotics disrupt bacterial cells wall & kill bacteria
gene mutations have led to production of functional proteins that result in antibiotic resistance
r plasmids carry f-factor — can pass it on
how to gene mutations negate the effects of antibiotics
blocking uptake of antibiotic into the bacterium
enzymatically breaking down the antibiotic before it is taken up
transduction
bacterial DNA is transferred from one bacterium to another on the back of bacteriophage particles
how does the mechanism for transduction work
during lytic cycle of bacteriophage virus the bacterial DNA is degreades & small piece is packaged into capsid as new bacteriophage is assembled
makes it useless
the bit of DNA can now be incorporated into new bacterial host & genes can be expressed
genetic engineering
recombining DNA from two different sources for commercial use
dna cloning