Lankford C E, Walker J R, Reeves J B, Nabbut N H, Byers B R, Jones R J
J Bacteriol. 1966 Mar;91(3):1070-9. doi: 10.1128/jb.91.3.1070-1079.1966.
Lankford, C. E. (The University of Texas, Austin), James R. Walker, James B. Reeves, N. H. Nabbut, B. R. Byers, and R. J. Jones. Inoculum-dependent division lag of Bacillus cultures and its relation to an endogenous factor(s) ("schizokinen"). J. Bacteriol. 91:1070-1079. 1966.-When cells of Bacillus megaterium, grown on Brain Heart Infusion Agar, were inoculated into a chemically defined medium, they exhibited a division lag which was an inverse function of inoculum size. The addition of filtrates of cultures from the same medium eliminated the inoculum-dependent component of lag, but not an inoculum-independent residual lag of constant duration. Culture filtrate of B. subtilis var. niger not only eliminated its inoculum-dependent lag but also was required to sustain exponential division. Dose-response and "growth time" bioassays, developed to measure lag-reducing activity of filtrates, demonstrated accumulation of active filtrate factor to a "critical" concentration prior to division initiation. Addition of this concentration to cultures eliminated the inoculum-dependent lag. Accumulation of the factor ceased temporarily at onset of division, but excretion was resumed later during exponential growth. Accumulation of a lag-reducing, cell-associated factor followed a similar course. Chromatographic and bioautographic analyses of culture filtrates of B. megaterium indicated that a single substance was primarily responsible for their activity. Results of dose-response tests for reciprocal activities of filtrates of different Bacillus species and strains suggested production of different factors by some, and of different quantities of similar factors by others. It is proposed that such endogenous factors which are synthesized and accumulate to a population-dependent concentration as a requisite to initiation and maintenance of division be designated as "schizokinens."
兰克福德,C.E.(得克萨斯大学奥斯汀分校),詹姆斯·R.沃克、詹姆斯·B.里夫斯、N.H.纳布特、B.R.拜尔斯和R.J.琼斯。巨大芽孢杆菌培养物接种量依赖性分裂延迟及其与内源性因子(“裂殖素”)的关系。《细菌学杂志》91:1070 - 1079。1966年。——当在脑心浸液琼脂上生长的巨大芽孢杆菌细胞接种到化学成分明确的培养基中时,它们表现出分裂延迟,且该延迟是接种量大小的反函数。添加来自同一培养基的培养物滤液可消除延迟中接种量依赖性成分,但不能消除持续时间恒定的接种量非依赖性残余延迟。枯草芽孢杆菌黑色变种的培养滤液不仅消除了其接种量依赖性延迟,而且是维持指数分裂所必需的。为测量滤液延迟减少活性而开发的剂量反应和“生长时间”生物测定表明,在分裂开始前,活性滤液因子积累到“临界”浓度。向培养物中添加该浓度可消除接种量依赖性延迟。该因子的积累在分裂开始时暂时停止,但在指数生长后期又恢复分泌。一种与细胞相关的延迟减少因子的积累过程与之相似。巨大芽孢杆菌培养滤液的色谱和生物自显影分析表明,一种单一物质是其活性的主要原因。不同芽孢杆菌种类和菌株滤液相互活性的剂量反应测试结果表明,一些菌株产生不同的因子,另一些菌株产生不同数量的相似因子。有人提出,这种内源性因子在合成并积累到群体依赖性浓度后,作为启动和维持分裂的必要条件,应被命名为“裂殖素”。