Jenkinson H F
Department of Oral Biology and Oral Pathology, University of Otago, Dunedin, New Zealand.
J Gen Microbiol. 1987 Jul;133(7):1909-18. doi: 10.1099/00221287-133-7-1909.
Mutants of Streptococcus sanguis resistant to novobiocin (NovR-mutants) were isolated after mutagenesis of strain Challis with ethyl methanesulphonate. The resistance phenotype was transferred by DNA-mediated transformation back into the parent strain at high frequency suggesting resistance was due to mutation(s) in a single gene or in closely-linked genes. Cells of NovR-mutants had normal morphology and secreted similar proteins to the wild-type strain. However, mutant cultures had slower growth rates, the mutant cells had reduced hydrophobicity, and they showed a reduced degree of coaggregation with Actinomyces viscosus and Actinomyces naeslundii. Cell envelopes prepared from NovR-mutants differed from wild-type cell envelopes in that they (a) were impaired in ability to coaggregate with A. viscosus cells, and (b) had altered protein composition as detected by SDS-PAGE. The results suggest that hydrophobic proteins in the cell envelope of S. sanguis may be necessary for coaggregation of this bacterium with actinomycetes.
用甲磺酸乙酯对血链球菌Challis菌株进行诱变后,分离出了对新生霉素具有抗性的血链球菌突变体(NovR突变体)。通过DNA介导的转化,抗性表型以高频转移回亲本菌株,这表明抗性是由于单个基因或紧密连锁基因中的突变所致。NovR突变体的细胞具有正常的形态,并且分泌与野生型菌株相似的蛋白质。然而,突变体培养物的生长速率较慢,突变体细胞的疏水性降低,并且它们与粘性放线菌和内氏放线菌的共聚程度降低。从NovR突变体制备的细胞膜与野生型细胞膜不同,在于它们(a)与粘性放线菌细胞共聚的能力受损,并且(b)通过SDS-PAGE检测到蛋白质组成发生了改变。结果表明,血链球菌细胞膜中的疏水蛋白可能是该细菌与放线菌共聚所必需的。