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球形芽孢杆菌9602的细胞壁聚合物。II. 芽孢形成过程中皮层合成特有的第一种酶的合成。

Cell wall polymers of Bacillus sphaericus 9602. II. Synthesis of the first enzyme unique to cortex synthesis during sporulation.

作者信息

Tipper D J, Pratt I

出版信息

J Bacteriol. 1970 Aug;103(2):305-17. doi: 10.1128/jb.103.2.305-317.1970.

Abstract

The cell wall peptidoglycan of vegetative cells of Bacillus sphaericus 9602 contains l-lysine and d-isoasparagine and is devoid of diaminopimelic acid (Dap), whereas the peptidoglycan of its spore cortex is devoid of l-lysine and d-isoasparagine and contains meso-Dap. These two structures have a common biosynthetic precursor, uridine-diphospho-N-acetylmuramyl-l- alanyl-d-glutamic acid, which accepts either l-lysine or meso-Dap, the latter reaction being the first unique to the synthesis of the spore cortex peptidoglycan. l-lysine-adding activity decays at the end of vegetative growth to a level which is maintained until Dap-adding activity appears, when it declines rapidly again. Dap-adding activity is not detectable in refractile spores, in vegetative cells, or in sporulating cells until about 4 hr after the end of vegetative growth, when it increases rapidly for about 1.5 hr in a process dependent on continued protein and ribonucleic acid (RNA) synthesis. This process apparently involves transcription and translation during this period of a "sporulation-specific" gene whose product is essential for and unique to sporulation. It is closely followed by the acquirement of refractility. Another sporulation-specific gene, that for dipicolinate synthase, is apparently transcribed and translated in an overlapping period commencing about 0.5 hr later, although dipicolinate does not accumulate rapidly until 1.5 hr later, when about 75% of the cells are already refractile. Inhibition of protein synthesis with chloramphenicol or of RNA synthesis with streptolydigin inhibited accumulation of these enzymes in sporulating cells; this inhibition could be reversed by washing out the antibiotics after 1.5 hr. Sporulation recommenced with an unaltered sequence of events but with poorer synchrony. There was no evidence for a messenger RNA for either enzyme of lifetime greater than a small fraction of the period of enzyme accumulation, although dilution with 10 volumes of fresh medium failed to prevent synthesis of Dap-adding enzyme in cells which had become terminally swollen, a process preceding enzyme synthesis by about 1.5 hr. The synthesis of this enzyme in B. sphaericus is apparently dependent on programmed transcription of the appropriate gene.

摘要

球形芽孢杆菌9602营养细胞的细胞壁肽聚糖含有L-赖氨酸和D-异天冬酰胺,不含二氨基庚二酸(Dap),而其芽孢皮层的肽聚糖不含L-赖氨酸和D-异天冬酰胺,含有内消旋-Dap。这两种结构有一个共同的生物合成前体,尿苷二磷酸-N-乙酰胞壁酰-L-丙氨酰-D-谷氨酸,它可以接受L-赖氨酸或内消旋-Dap,后一种反应是芽孢皮层肽聚糖合成所特有的第一个反应。添加L-赖氨酸的活性在营养生长末期下降到一个维持水平,直到添加Dap的活性出现,此时它又迅速下降。直到营养生长结束后约4小时,在折光性孢子、营养细胞或芽孢形成细胞中都检测不到添加Dap的活性,此时它在一个依赖于持续蛋白质和核糖核酸(RNA)合成的过程中迅速增加约1.5小时。这个过程显然涉及在这个时期转录和翻译一个“芽孢形成特异性”基因,其产物对芽孢形成至关重要且是芽孢形成所特有的。紧接着是获得折光性。另一个芽孢形成特异性基因,即吡啶二羧酸合酶基因,显然在大约0.5小时后开始的一个重叠时期进行转录和翻译,尽管吡啶二羧酸直到1.5小时后才迅速积累,此时约75%的细胞已经具有折光性。用氯霉素抑制蛋白质合成或用利福平抑制RNA合成会抑制芽孢形成细胞中这些酶的积累;1.5小时后洗去抗生素可以逆转这种抑制。芽孢形成以未改变的事件顺序重新开始,但同步性较差。没有证据表明这两种酶的信使RNA的寿命大于酶积累期的一小部分,尽管用10倍体积的新鲜培养基稀释并不能阻止在已经最终肿胀的细胞中合成添加Dap的酶,这个过程比酶合成早约1.5小时。球形芽孢杆菌中这种酶的合成显然依赖于适当基因的程序性转录。

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