Round 5: Tossup 17

A key step of the “SeSaM” version of this technique is strand cleavage at phosphorothioate (“phosphor-oh-thio-ate”) groups followed by amplification with TdT. The “insertional” form of this technique uses P-element or Sleeping Beauty transposons. One form of this technique transforms DUT and UDG deficient E. coli strains with M13 phagemids and was developed by Thomas Kunkel. Alanine scanning is a diagnostic form of this technique, which can be done randomly (10[1])using ethyl nitrosoureas (“nitroso-ureas”). A form of this technique uses a variant of PCR with manganese ions instead of magnesium (10[1])ones to coordinate “sloppy” Taq polymerases. Stratagene developed the “Quikchange” kit for the “site-directed” form of this technique. For 10 points, name this technique for introducing sequence changes into a target genome. ■END■ (0[4])

ANSWER: mutagenesis [accept saturation or insertional or random or site-directed mutagenesis; accept answers involving making mutations; accept error-prone PCR or epPCR until read; prompt on polymerase chain reaction or PCR until read by asking “what is that being used to accomplish?”; prompt on directed evolution by asking “what technique is used to drive that?”] (The first sentence refers to sequence saturation mutagenesis.)
<AL, Biology> | Packet G - McMaster A, Notre Dame C, Rutgers A, NYU A
= Average correct buzzpoint

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Buzzes


Summary

TournamentEditionMatchHeardConv. %Neg %Avg. Buzz
California (North)Main Site367%0%68.00
California (South)Main Site450%0%77.50
CanadaMain Site1145%18%98.60
FloridaMain Site333%0%101.00
Great LakesMain Site560%40%91.67
Lower Mid-AtlanticMain Site911%11%105.00
MidwestMain Site850%25%104.25
NortheastMain Site683%0%105.60
OverflowMain Site425%0%120.00
South CentralMain Site20%0%
SoutheastMain Site838%25%104.00
UKMain Site1250%17%100.00
Upstate NYMain Site40%50%