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嗜中温产碱菌氢化酶基因的转录调控

Transcriptional regulation of Alcaligenes eutrophus hydrogenase genes.

作者信息

Schwartz E, Gerischer U, Friedrich B

机构信息

Institut für Biologie, Humboldt-Universität zu Berlin, Germany. edward=

出版信息

J Bacteriol. 1998 Jun;180(12):3197-204. doi: 10.1128/JB.180.12.3197-3204.1998.

Abstract

Alcaligenes eutrophus H16 produces a soluble hydrogenase (SH) and a membrane-bound hydrogenase (MBH) which catalyze the oxidation of H2, supplying the organism with energy for autotrophic growth. The promoters of the structural genes for the SH and the MBH, PSH and PMBH, respectively, were identified by means of the primer extension technique. Both promoters were active in vivo under hydrogenase-derepressing conditions but directed only low levels of transcription under condition which repressed hydrogenase synthesis. The cellular pools of SH and MBH transcripts under the different growth conditions correlated with the activities of the respective promoters. Also, an immediate and drastic increase in transcript pool levels occurred upon derepression of the hydrogenase system. Both promoters were dependent on the minor sigma factor sigma 54 and on the hydrogenase regulator HoxA in vivo. PSH was stronger than PMBH under both heterotrophic and autotrophic growth conditions. The two promoters were induced at approximately the same rates upon derepression of the hydrogenase system in diauxic cultures. The response regulator HoxA mediated low-level activation of PSH and PMBH in a heterologous system.

摘要

嗜糖假单胞菌H16产生一种可溶性氢化酶(SH)和一种膜结合氢化酶(MBH),它们催化H2的氧化,为该生物体的自养生长提供能量。分别通过引物延伸技术鉴定了SH和MBH结构基因的启动子PSH和PMBH。在氢化酶去阻遏条件下,这两个启动子在体内均具有活性,但在抑制氢化酶合成的条件下仅指导低水平的转录。不同生长条件下SH和MBH转录本的细胞池与各自启动子的活性相关。此外,氢化酶系统去阻遏后,转录本池水平立即急剧增加。在体内,这两个启动子均依赖于次要的σ因子σ54和氢化酶调节因子HoxA。在异养和自养生长条件下,PSH均强于PMBH。在双相培养中,氢化酶系统去阻遏后,这两个启动子以大致相同的速率被诱导。响应调节因子HoxA在异源系统中介导PSH和PMBH的低水平激活。

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