首页 | 本学科首页   官方微博 | 高级检索  
     


Molecular characterization of thirteen gyrA mutations conferring nalidixic acid resistance in Bacillus subtilis
Authors:N. Munakata   F. Morohoshi   M. Saitou   N. Yamazaki  K. Hayashi
Affiliation:(1) Radiobiology Division, National Cancer Center Research Institute, Tsukiji, 5-1-1, 104 Chuo-ku, Tokyo, Japan;(2) Oncogene Division, National Cancer Center Research Institute, Tsukiji, 5-1-1, 104 Chuo-ku, Tokyo, Japan;(3) Present address: Institute for Environmental Sciences, Aomori, Japan;(4) Present address: Department of Biological Science, Tokyo Institute of Technology, Yokohama, Japan;(5) Present address: Institute of Experimental Gene Informatics, Kyushu University, Fukuoka, Japan
Abstract:We isolated 607 independent nalidixic acid-resistant mutants from Bacillus subtilis. A 163 by DNA segment from a 5prime portion of the gyrA gene was amplified from the DNA of each mutant strain. After heat denaturation, the product was subjected to gel electrophoresis to detect conformational polymorphism of single-strand DNA (PCR-SSCP analysis). Mobility patterns of the two DNA strands from all the mutant strains examined differed from those of the parental wild-type strains. The patterns were classified into 13 types, and the DNA sequence of each type was determined. A unique sequence alteration was found in mutants belonging to each of the 13 types, defining 13 gyrA alleles. Eight were single base pair substitutions, four were substitutions of two consecutive base pairs, and one was a substitution of three consecutive base pairs. Only three amino acid residues (Ser-84, Ala-85, and Glu-88) were altered in the deduced amino acid sequences of the mutated genes. We conclude that molecular typing based on the PCR-SSCP method is a powerful technique for the exhaustive identification of allelic variants among mutants selected for a phenotypic trait.
Keywords:DNA gyrase A subunit  Bacillus subtilis Nalidixic acid  Single-strand conformation polymorphisms
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号