Genetic transformation in Streptococcus sanguis. Kinetics of production in different media and specific interaction of competence factor and competence factor inactivator.

P Gaustad
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Abstract

The production and the persistence of competence factor (CF) and competence factor inactivator (CFI) of four different strains of Streptococcus sanguis in three media (Todd Hewitt broth, medium II and medium IV) have been examined with respect to kinetics. Both the medium used and the strains examined offered implications on the activities of CF and CFI. CF was not detectable in the culture filtrates of strains Wicky (NCTC 9124) and 445. Strain Blackburn (NCTC 10231) showed activity only in Todd Hewitt broth and strain 14567 in Todd Hewitt broth and medium IV. The activity persisted for 2 to 7 hours during exponential growth. In culture filtrates of the strains Wicky and Blackburn the three media yielded high CFI activity persisting during the entire growth period. The strains 445 and 14567 were less potent CFI producers in medium II and medium IV, and no CFI was detected in the culture filtrates from Todd Hewitt broth. Medium II was the most suitable medium for CFI production and seems appropriate for further studies and isolation of the factor. In medium IV no strain had CF activity. This medium was supplemented with serum, albumin, tyrosine or glutamic acid, and CF and CFI production and persistence by strain 14567 were studied in relation to growth phases. CF and CFI activities were observed in the different supplemented media during short periods of growth, but could not be related to any given phase of growth. The presence of CFI in a culture eliminated or reduced the CF activity, and a specific interaction of CF and CFI was observed. The CFI from the strain Wicky inactivated CF from the strains Challis (NCTC 7868) and Blackburn, but not from the strains 13b and 14567. The CFI from the strains 445 and 14567 reduced the activity of CF produced by the strains 13b and 14567, but not CF from the strains Challis and Blackburn.

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血链球菌的遗传转化。能力因子与能力因子失活剂在不同介质中的生产动力学及特定的相互作用。
研究了四种不同血链球菌菌株在三种培养基(托德休伊特肉汤、培养基II和培养基IV)中能力因子(CF)和能力因子灭活剂(CFI)的产生和持续动力学。所使用的培养基和菌株对CF和CFI的活性都有影响。菌株Wicky (NCTC 9124)和菌株445的培养滤液中未检出CF。菌株Blackburn (NCTC 10231)仅在Todd Hewitt培养液中表现出活性,菌株14567在Todd Hewitt培养液和培养基IV中表现出活性。在指数生长期间,活性持续2 ~ 7小时。在菌株Wicky和Blackburn的培养滤液中,这三种培养基在整个生长期间都具有较高的CFI活性。菌株445和14567在培养基II和培养基IV中产生CFI的能力较弱,在Todd Hewitt肉汤培养滤液中未检测到CFI。培养基II是最适合生产CFI的培养基,似乎适合进一步研究和分离该因子。在中等静脉注射中,没有菌株具有CF活性。在培养基中添加血清、白蛋白、酪氨酸或谷氨酸,研究菌株14567的CF和CFI产量和持久性与生长阶段的关系。在不同的培养基中,CF和CFI活性在短时间内都可以观察到,但与任何特定的生长阶段都没有关系。CFI在培养物中的存在消除或降低了CF活性,并且观察到CF和CFI的特定相互作用。菌株Wicky的CFI灭活了菌株Challis (NCTC 7868)和Blackburn的CF,但没有灭活菌株13b和14567的CF。菌株445和14567的CFI降低了菌株13b和14567的CF活性,而菌株Challis和Blackburn的CF活性没有降低。
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