Ruby E G, Rittenberg S C
J Bacteriol. 1983 Apr;154(1):32-40. doi: 10.1128/jb.154.1.32-40.1983.
Bdellovibrio bacteriovorous attacks and penetrates other gram-negative bacteria, creating a growth chamber termed a bdelloplast. We have found that exposing the bdelloplasts to EDTA, followed by treatment with a lytic enzyme concentrate derived from bdellovirio cultures, prematurely released the intraperiplasmically growing bdellovibrios at any time during their growth cycle. Upon release, the growth-form bdellovibrios terminated any initiated rounds of DNA synthesis and differentiated into motile attack-form cells. The ability of growth-form cells to synthesize DNA appears to depend upon an initiation signal that is not received until about 60 min after attack. Each subsequent round of DNA synthesis by the growing bdellovibrio filaments seems to require an additional initiation signal that is provided by their intraperiplasmic environment. Differentiation included fragmentation into multiple progeny cells to a degree proportional to the extent of intraperiplasmic growth. This differentiation could be performed totally at the expense of cellular reserves. The significance of these data to an understanding of the regulation of differentiation in bdellovibrios is discussed.
食菌蛭弧菌会攻击并穿透其他革兰氏阴性菌,形成一个称为蛭质体的生长腔室。我们发现,将蛭质体暴露于乙二胺四乙酸(EDTA),随后用源自蛭弧菌培养物的溶菌酶浓缩物进行处理,会在其生长周期的任何时候过早释放出在周质内生长的蛭弧菌。释放后,生长型蛭弧菌会终止任何已启动的DNA合成轮次,并分化为运动攻击型细胞。生长型细胞合成DNA的能力似乎取决于一个直到攻击后约60分钟才会接收到的起始信号。生长中的蛭弧菌丝随后的每一轮DNA合成似乎都需要由其周质内环境提供的额外起始信号。分化包括分裂成多个子代细胞,其程度与周质内生长的程度成比例。这种分化可以完全以细胞储备为代价进行。本文讨论了这些数据对于理解蛭弧菌分化调控的意义。