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通过高分辨率放射自显影研究巨大芽孢杆菌孢子肽聚糖的合成。

Bacillus megaterium sporal peptidoglycan synthesis studied by high-resolution autoradiography.

作者信息

Frehel C, Ryter A

出版信息

J Bacteriol. 1980 Nov;144(2):789-99. doi: 10.1128/jb.144.2.789-799.1980.

Abstract

Cells of a Dap- Lys- mutant strain of Bacillus megaterium were pulse labeled with [3H]diaminopimelic acid at different times of growth and sporulation. They were processed for radioactivity measurements and high-resolution autoradiography either just after the pulse or after a chase in a nonradioactive medium until refractile forespores started to appear at time (t)4,5. In the pulse-labeled cells, autoradiographs and radioactivity measurements showed that the radioactivity incorporated during a pulse decreased abruptly after t0 and stayed at a low level until t5, although the forespore wall and cortex were formed between t4 and t5. In the pulse-chased bacteria, the acid-insoluble radioactivity, as well as the number of silver grains on autoradiographs, increased during the chase in cells labeled at t1 to t2, whereas it decreased in those labeled before t0. Furthermore, analysis of silver grain distribution showed that, in stage IV bacteria, grains were distributed at the outside of the forespore, mostly on the sporangium cell wall, when pulse-labeling occurred before or at t0; they were located along the cortex and in the forespore cytoplasm when labeling was made at t1 or t2. These facts show that [3H]diaminopimelic acid necessary for spore envelope synthesis was incorporated before their morphological appearance. Free or small diaminopimelic acid precursors entered the sporangium between t1 and t2. The appearance of silver grains in the forespore cytoplasm suggests that the forespore is implicated in sporal peptidoglycan synthesis.

摘要

巨大芽孢杆菌的Dap-Lys-突变菌株细胞在生长和芽孢形成的不同时间用[3H]二氨基庚二酸进行脉冲标记。在脉冲后或在无放射性培养基中追踪后,直到在时间(t)4,5出现折射前芽孢,对它们进行放射性测量和高分辨率放射自显影处理。在脉冲标记的细胞中,放射自显影和放射性测量表明,脉冲期间掺入的放射性在t0后突然下降,并保持在低水平直到t5,尽管前芽孢壁和皮层在t4和t5之间形成。在脉冲追踪的细菌中,酸不溶性放射性以及放射自显影片上的银粒数量,在对t1至t2标记的细胞进行追踪期间增加,而在t0之前标记的细胞中则减少。此外,银粒分布分析表明,在IV期细菌中,当在t0之前或t0时进行脉冲标记时,银粒分布在前芽孢外部,主要在孢子囊细胞壁上;当在t1或t2进行标记时,它们位于皮层和前芽孢细胞质中。这些事实表明,孢子包膜合成所需的[3H]二氨基庚二酸在其形态出现之前就已掺入。游离或小的二氨基庚二酸前体在t1和t2之间进入孢子囊。前芽孢细胞质中银粒的出现表明前芽孢参与了孢子肽聚糖的合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfe9/294730/7a321813cb6b/jbacter00572-0314-a.jpg

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