Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD 20742, USA.
BMC Microbiol. 2009 Nov 23;9:239. doi: 10.1186/1471-2180-9-239.
Organisms that are sensitive to nitrofurantoin express a nitroreductase. Since bacterial resistance to this compound results primarily from mutations in the gene encoding nitroreductase, the resulting loss of function of nitroreductase results in a selectable phenotype; resistance to nitrofurantoin. We exploited this direct selection for mutation to study the frequency at which spontaneous mutations arise (transitions and transversions, insertions and deletions).
A nitroreductase- encoding gene was identified in the N. gonorrhoeae FA1090 genome by using a bioinformatic search with the deduced amino acid sequence derived from the Escherichia coli nitroreductase gene, nfsB. Cell extracts from N. gonorrhoeae were shown to possess nitroreductase activity, and activity was shown to be the result of NfsB. Spontaneous nitrofurantoin-resistant mutants arose at a frequency of approximatelty 3 x 10(-6) - 8 x 10(-8) among the various strains tested. The nfsB sequence was amplified from various nitrofurantoin-resistant mutants, and the nature of the mutations determined. Transition, transversion, insertion and deletion mutations were all readily detectable with this reporter gene.
We found that nfsB is a useful reporter gene for measuring spontaneous mutation frequencies. Furthermore, we found that mutations were more likely to arise in homopolymeric runs rather than as base substitutions.
对呋喃妥因敏感的生物体表达硝基还原酶。由于细菌对该化合物的抗性主要是由于编码硝基还原酶的基因发生突变,因此硝基还原酶的功能丧失导致可选择的表型;对呋喃妥因的抗性。我们利用这种直接选择突变的方法来研究自发突变的频率(转换和颠换、插入和缺失)。
通过使用源自大肠杆菌硝基还原酶基因 nfsB 的推导氨基酸序列的生物信息学搜索,在淋病奈瑟菌 FA1090 基因组中鉴定出了一个硝基还原酶编码基因。从淋病奈瑟菌中提取的细胞提取物显示具有硝基还原酶活性,并且该活性是 NfsB 的结果。在各种测试的菌株中,自发产生的呋喃妥因抗性突变体的出现频率约为 3x10(-6) - 8x10(-8)。从各种呋喃妥因抗性突变体中扩增了 nfsB 序列,并确定了突变的性质。通过这个报告基因,很容易检测到转换、颠换、插入和缺失突变。
我们发现 nfsB 是测量自发突变频率的有用报告基因。此外,我们发现突变更可能发生在同聚核苷酸序列中,而不是碱基取代。