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Genetics Ch 9

Microbiology Ch 9 Study

QuestionAnswer
Genetics Broad: Science that studies the inheritance of biological characteristics by living things.
Deoxyribonucleic acid (DNA) is a nucleic acid containing genetic instructions used in dev and functioning of living org's(except RNA viruses). Genes carry genetic info but other DNA seq's have structural purpose or are inv in regulating gene expression.
DNA Structure nucleotide: ~phosphate ~deoxyribose sugar ~nitrogenous base DOUBLE HELIX
Genome sum total of genetic material carried within a cell
Plasmids A DNA molecule that is separate from and can replicate independently of the chromosomal DNA. Mainly DS and circular. USU occur in bacteria but are sometimes found in eukaryotes.
Chromosome discrete cellular structure composed of a neatly packaged DNA molecule
Gene a specific segment of DNA that contains the necessary codes to produce proteins or an RNA molecule
Genotype sum of all types of genes in an organisms genetic make-up (only some expressed)
Phenotype Expression of genotype creating traits--changes depending on which genes are "turned on" or expressed.
Purine A nitrogen base that is an important encoding component of DNA and RNA. The 2 most common: Adenine & Guanine
Pyrimidine Nitrogen bases that help form the genetic code on DNA and RNA. Uracil, thymine, and cytosine are the most prevalent.
Pyrimidine dimer The union of 2 adjacent pyrimidines on the same DNA strand, brought about by exposure to UV light. It is a form of mutation.
Paired bases The pairing of purine bases in one DNA strand to pyrimidine bases in another DNA/RNA strand. Held together by weak hydrogen bonds.
Adenine : Thymine pairing Forms 2 hydrogen bonds and is the site for DNA "unzipping" to begin synthesis.
Guanine : Cytosine pairing Forms 3 hydrogen bonds
antiparallel arrangement Term used to describe the asymmetrical orientation of paired helixes in opposite directions. One side runs 3' to 5' and the other side 5' to 3'
DNA replication The process of duplication of DNA coding in high fidelity to pass genetics through generations of organisms.
Helicase Fx: Unzipping the DNA helix
Primase Fx: Synthesizing an RNA primer
DNA polymerase III FX: Adding basses to the new DNA chain; proofreading the chain for mistakes
DNA polymerase I Fx: Removing RNA primer, closing gaps, repairing mismatches
Ligase Fx: Final binding of nicks in DNA during synthesis and repair
Gyrase Supercoiling
Semiconservative replication Produces two copies that each contained one of the original parent strands of DNA and one new strand
DNA Polymerase III Constrictions *cannot add nucleotides to a DNA strand w/o a preexisting unbound nucleotide *RNA primer must be inserted at the origin of replication *Can add nucleotides only in 5' to 3'
Replication forks Due to the circular shape of a bacterial DNA molecule, opening of the circle forms a Y shaped point of DNA synthesis on both ends of DNA synthesis process
Leading Strand The newly forming 39' DNA strand that is replicated in a continuous fashion without segments
Lagging strand The newly forming 59' DNA strand that is discontinuously replicated in segments (Okazaki fragments).
Transcription mRNA synthesis; the process by which a strand of RNA is produced against a DNA template.
Translation Protein synthesis; the process of decoding the mRNA code into a polypeptide.
triplets (aka codon) A specific sequence of 3 nucleotides in mRNA (or the sense strand in DNA) that constitutes the genetic code for a particular amino acid
ribonucleic acid (RNA) The nucleic acid responsible for carrying out the hereditary program transmitted by an organism's DNA
anticodon The trinucleotide sequence of tRNA that is complimentary to the trinucleotide
RNA Polymerase Large enzyme complex responsible for DNA code synthesis of RNA during transcription. *Works without the need of helicase (unlike DNA), it can bind to DNA, unwind it and synthesize the RNA.
promoter region The site composed of a short signaling DNA sequence that RNA polymerase recognizes and combines to commence transcription.
Transcription Stages initiation, elongation, and termination
nontemplate DNA in RNA synthesis - does not carry a message that can be translated to a protein
Start codon as ribosomes begin scanning the mRNA by moving 5' to 3' direction--translation begins when "AUG" codon is encountered
STOP CODONS UAA, UAG, UGA
Degeneracy (aka Redundancy) The property of the genetic code that allows an amino acid to be specified by several different codons.
Nonsense / Stop Codons Termination codons UAA, UAG, UGA for where there is no corresponding anticodon--stop synthesis
Polyribosomal Complex Length of mRNA allots feeding through more than 1 ribosome simultaneously; permits synthesis of 100's protein mol's.
Introns The segments on split genes of eukaryotes that do not code for polypeptide. They can have regulatory function (see exon).
Exon A stretch of eukaryotic DNA coding for a corresponding portion of mRNA that is not translated into peptides. During transcription, exons are separated from introns & spliced together-continuous mRNA transcript.
Operons Prokaryotic form of gene regulation: section of DNA that contains one or more structural genes along w/corresponding operator gene that controls transcription.
Inducible (Operon) "OFF" norm - catabolic operon turned on (when needed) by the substrate of the enzyme for which the structural genes code. (e.g. lactose)
Respressible (Operon) "ON norm" -anabolic operon turned off only when the product of the pathway is no longer required (arginine)
corepressor excess product within a cell that slows down the transcription of an operon
Mutation A phenotypic change due to an alteration in genotype - an alteration of the nitrogen base sequences of DNA.
Wild Type Original, nonmutated sequencing of genomes.
Mutant Strain (mutation) Show variance in morphology, nutritional characteristics, genetic control mech, resistance to chemicals, temperature preference, & almost any type of enzymatic fx.
Spontaneous mutation a random change in DNA arising from errors in replication that occur without a known cause
Induced mutations mutations resulting from exposure to known mutagens
mutagens primarily physical or chemical agents that damage DNA and interfere with its functioning
Point mutations small mutations that affect only a single base on a gene- involve addition, deletion, or substitution of SINGLE bases
Missense mutation ANY change in the DNA code and copied to mRNA that leads to placement of different amino acid... 1)create a faulty, nonfx protein 2)prod a protein that fx in a different way or 3)cause no significalt alt to protein fx
Nonsense mutation Changes a normal codon into a STOP codon = stops the production of protein (almost ALWAYS results in a nonfx protein)
Silent mutation alters the base but does not change the amino acid and has no effect on synthesis
Back-mutation Occurs when a gene that has mutated reverts back to its original base composition
Frameshift (mutation) One or more bases insterted into or deleted from a newly synthesized DNA strand thus changing reading of every aa = nonfx protein
Ames test Method for detecting mutagenic agents based upon alteration of nutritionally defective bacteria
histidine (His or H) essential amino acid containing a positively charged imidazole functional group.
Conjugation attachment of 2 related species and the formation of a pilus to transport DNA
Transformation Lysed donor cell releases naked DNA fragments to any competent receptor cell
Transduction transfer by means of bacteriophage vector from donor lysed bacterial cell - live receptor cell of the same species
Competent (via transduction) cells capable of receiving genetic material by the use of special DNA Binding proteins located on the cell wall
transposons A DNA segment with an insertion sequence at each end, enabling it to migrate to another plasmid, to the bacterial chromosome, or to a bacteriophage
Bacteriophage A virus that specifically attacks bacteria
Created by: JaeLaw23
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