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微生物孢子。二十六。阻止生长的蜡样芽孢杆菌萌发孢子的合成活性。

Spores of microorganisms. XXVI. Synthetic activities of germinating spores of Bacillus cereus prevented from outgrowth.

作者信息

Stastná J, Vinter V

出版信息

Folia Microbiol (Praha). 1975;20(3):195-205. doi: 10.1007/BF02876779.

Abstract

Spores of Bacillus cereus were germinated in a germination limited medium (GL-medium) which facilitates only germination but not the postgerminative development of spores. Under these conditions a limited protein synthesis occurs. However, this protein synthesis is stopped after a short time interval. The rate of synthesis of new proteins, as well as their total amount, is influenced by the length of the activation heat shock. Synthesis of the wall material continues for several hours and thick-walled cells with a changed ultrastructure are formed. Synthesis of the diaminopimelic acid (dap) containing material of the cell wall is sensitive to actinomycin D and relatively resistant to chloramphenicol. Similarly, protein synthesis is relatively chlorapmhenicol-resistant but is fully inhibited by azauracil or spiramycin. Whereas RNA formed in the control culture is partially decomposed after 30 min of incubation, chloramphenicol accelerates its synthesis and prevents its decay. Exudate components apparently stimulate synthesis of ribonucleic acid, proteins and the wall material. The 14-C-dap containing material released by prelabelled spores in the form of the exudate during the germination is not re-utilized by the spores germinated in the GL-medium. The results are discussed with respect to the atypical primary synthetic activities of spores under conditions when the postgerminative development is prevented and from the point of view of participation of the germination exudate during these syntheses.

摘要

蜡样芽孢杆菌的孢子在发芽受限培养基(GL-培养基)中发芽,该培养基仅促进孢子发芽,而不促进孢子发芽后的发育。在这些条件下会发生有限的蛋白质合成。然而,这种蛋白质合成在短时间间隔后就会停止。新蛋白质的合成速率及其总量受激活热休克时间长短的影响。壁物质的合成会持续数小时,并形成具有改变的超微结构的厚壁细胞。细胞壁中含二氨基庚二酸(dap)物质的合成对放线菌素D敏感,对氯霉素相对抗性。同样,蛋白质合成对氯霉素相对抗性,但被氮杂尿嘧啶或螺旋霉素完全抑制。对照培养物中形成的RNA在孵育30分钟后会部分分解,而氯霉素会加速其合成并防止其降解。渗出物成分显然会刺激核糖核酸、蛋白质和壁物质的合成。在发芽过程中以渗出物形式由预先标记的孢子释放的含14-C-dap物质不会被在GL-培养基中发芽的孢子重新利用。从防止发芽后发育的条件下孢子的非典型初级合成活性以及发芽渗出物在这些合成过程中的参与角度对结果进行了讨论。

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