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The Molecular Basis of Inheritance

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2400064Oswald AveryThis person worked to identify the transforming substance. He purified various chemicals from heat-killed pathogenic bacteria, then tried to transform live nonpathogenic bacteria with each chemical.
2400065VirusThis is a little more than DNA (sometimes RNA) enclosed by a protective coat
2400066BacteriophagesThese are viruses that infect bacteria.
2400067PhagesBacteriophages
2400068Hershey-Chase ExperimentMix radioactively labeled phages with bacteria. The phages infect the bacterial cells. Agitate in a blender to separate phages outside the bacteria from the cells and their contents. Centrifuge the mixture so bacteria form a pellet at the bottom of the test tube. Measure the radioactivity in the pellet and the liquid.
2400069Erwin ChargaffThis person analyzed the base composition of DNA from a number of different organisms.
2400070Chargaff's rules# of A=T and # of G=C
2400071DNAThis is a polymer of nucleotides.
2400072NucleotideThis has a nitrogenous base, deoxyribose, and a phosphate group.
2400073Watson and CrickThis person (these people) discovered the double helix by building models to conform to X-ray data.
2400074Rosalind FranklinThis person was an X-ray crystallographer and took the photo that some person (people) used to get the double-helical structure of DNA.
2400075PyrimidinesThe family of nitrogenous bases that have a single ring.
2400076PurinesThe family of nitrogenous bases that have two organic rings.
2400077Conservative modelThe parental double helix reamins intact and an all-new copy is made.
2400078Semiconservative modelThe two strands of the parental molecule separate, and each functions as a template for synthesis of a new complementary strand.
2400079Dispersive modelEach strand of both daughter molecules contains a mix of old and newly synthesized parts.
2400080Meselson-Stahl experimentThis tested the three models ofDNA replication by this: bacteria cutured in medium containing 15N and then is transferred to medium containing 14N. The different isotope of nitrogen was distinguishable so after DNA samples were centrifuged, one could tell which model was correct.
2400081Origins of replicationspecial sites where the replications of a DNA molecule begins
2400082replication forkThis is a Y-shaped region where the new strands of DNA are elongating.
2400083DNA polymerasesThese are enzymes that catalyze the elongation of new DNA at a replication fork.
24000843' endThis is where a hydroxyl group is attaced to the 3' carbon of the terminal deoxyribose.
24000855' endThis is where the sugar-phosphate backbone terminates with the phosphate group attached to the 5' carbon of the last nucleotide.
2400086where DNA polymerases add nucleotidesDNA polymerases add nucleotides only to the free 3' end of a growing DNA strand.
2400087Which direction do DNA strands elongate5' -> 3'
2400088leading strandThis strand is made first and is made completely at one time.
2400089Lagging strandThis strand is made starting from the direction away from the replication fork. This is synthesized in a series of short segments.
2400090Okazaki fragmentsThese are the series of segments first synthesized in the lagging strand.
2400091DNA ligaseThis ligates (joins) the sugar-phosphate backbones of the Okazaki fragments to create a single DNA strand.
2400092PrimerThis is the start of a new chain and is a short stretch of RNA.
2400093PrimaseThis is an enzyme that joins RNA nucleotides to make the primer. This can start an RNA chain from scratch.
2400094helicaseThis is an enzyme that untwists the double helix at the replication fork, separating the two old strands.
2400095single-strand binding proteinThese line up along the unpaired DNA strands, holding them apart while they serve as templates for the synthesis of new complementary strands.
2400256Frederick GriffithThis person made an experiment that involved injecting mice with smooth S cells, rough R cells, heat-killed S cells, and heat-killed S cells with living R cells.
2400257Mice LabMice were injected with pathogenic bacterium and variant bacterium. This experiment had apparently nothing to do with DNA, yet it hadeverything to do with DNA. This experiment was performed by Griffith.
2400258pathogenicdisease-causing
2400259variantharmless
2400260transformationThis is a change in genotype and phenotype due to the assimilation of external DNA by a cell.

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