Hoggarth J H, Ritchie D A
Department of Genetics and Microbiology, Donnan Laboratories, University of Liverpool, UK.
J Appl Bacteriol. 1995 May;78(5):543-7. doi: 10.1111/j.1365-2672.1995.tb03097.x.
RNA isolated at intervals during fermentation from the novobiocin-producing wild-type strain of Streptomyces niveus and from a series of novobiocin-non-producing (Nov-) mutants was hybridized to DNA probes containing sequences which specify novobiocin resistance. The probes were made from inserts contained in the clones pGL101 and pGL103 which increase the level of novobiocin resistance of S. lividans transformants from 10 micrograms ml-1 to 50 micrograms ml-1 and 150 micrograms ml-1, respectively. No hybridization was detected with the pGL101 probe. The pGL103 probe hybridized to RNA extracted during the later stages of growth--a pattern corresponding to the transition from low to high level novobiocin resistance during growth of S. niveus wild-type cultures. Neither probe hybridized to RNA extracted from four Nov- mutants. These mutants showed variable levels of novobiocin resistance but none expressed the high wild-type levels. The authors conclude that expression of the DNA sequence in pGL103 is associated with high level novobiocin resistance.
在发酵过程中,每隔一段时间从新霉素产生菌雪白链霉菌野生型菌株以及一系列不产生新霉素(Nov-)的突变体中分离出RNA,并将其与含有指定新霉素抗性序列的DNA探针杂交。这些探针由克隆pGL101和pGL103中的插入片段制成,它们分别将变铅青链霉菌转化体的新霉素抗性水平从10微克/毫升提高到50微克/毫升和150微克/毫升。未检测到与pGL101探针的杂交信号。pGL103探针与生长后期提取的RNA杂交——这种模式与雪白链霉菌野生型培养物生长过程中从低水平到高水平新霉素抗性的转变相对应。两种探针均未与从四个Nov-突变体中提取的RNA杂交。这些突变体表现出不同水平的新霉素抗性,但均未表达野生型的高水平抗性。作者得出结论,pGL103中的DNA序列表达与高水平新霉素抗性相关。