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Cloning and targeted mutagenesis of ...
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Ouyang, Ling.
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Cloning and targeted mutagenesis of a recA gene required for the extreme DNA damage-resistance of Deinococcus radiodurans.
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Cloning and targeted mutagenesis of a recA gene required for the extreme DNA damage-resistance of Deinococcus radiodurans./
作者:
Ouyang, Ling.
面頁冊數:
53 p.
附註:
Source: Masters Abstracts International, Volume: 33-06, page: 1786.
Contained By:
Masters Abstracts International33-06.
標題:
Biology, Microbiology. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1361765
Cloning and targeted mutagenesis of a recA gene required for the extreme DNA damage-resistance of Deinococcus radiodurans.
Ouyang, Ling.
Cloning and targeted mutagenesis of a recA gene required for the extreme DNA damage-resistance of Deinococcus radiodurans.
- 53 p.
Source: Masters Abstracts International, Volume: 33-06, page: 1786.
Thesis (M.S.)--The American University, 1994.
Deinococcus (D.) radiodurans and other members of the same bacterial family are extremely resistant to ionizing radiation, ultraviolet (UV)-radiation and many other DNA-damaging chemical agents. This unusual resistance stems from their extraordinarily efficient DNA repair mechanisms. A mutant strain (strain rec30) generated through chemical mutagenesis has been found to be both DNA-damage sensitive and natural transformation-defficient. Through gene complementation with wild-type (wt) genomic DNA, a gene with extended homology to the Escherichia coli recA was cloned. Transformation of the cloned deinococccal recA gene restored both the DNA-damage resistance and full natural transformation competence of the rec30 mutant. Targeted insertional mutagenesis of the deinococccal recA gene in wt D. radiodurans generated a mutant strain that was phenotypically indistinguishable from strain rec30. These results indicate that the observed phenotypic changes in strain rec30 were caused by a defect in its recA gene, and a RecA-mediated recombination repair pathway plays a critical role in the DNA repair of D. radiodurans.Subjects--Topical Terms:
1017734
Biology, Microbiology.
Cloning and targeted mutagenesis of a recA gene required for the extreme DNA damage-resistance of Deinococcus radiodurans.
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Deinococcus (D.) radiodurans and other members of the same bacterial family are extremely resistant to ionizing radiation, ultraviolet (UV)-radiation and many other DNA-damaging chemical agents. This unusual resistance stems from their extraordinarily efficient DNA repair mechanisms. A mutant strain (strain rec30) generated through chemical mutagenesis has been found to be both DNA-damage sensitive and natural transformation-defficient. Through gene complementation with wild-type (wt) genomic DNA, a gene with extended homology to the Escherichia coli recA was cloned. Transformation of the cloned deinococccal recA gene restored both the DNA-damage resistance and full natural transformation competence of the rec30 mutant. Targeted insertional mutagenesis of the deinococccal recA gene in wt D. radiodurans generated a mutant strain that was phenotypically indistinguishable from strain rec30. These results indicate that the observed phenotypic changes in strain rec30 were caused by a defect in its recA gene, and a RecA-mediated recombination repair pathway plays a critical role in the DNA repair of D. radiodurans.
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