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球形红细菌核酮糖二磷酸羧化酶/加氧酶缺陷型突变体中glnB和类glnB基因(glnK)的表达

Expression of glnB and a glnB-like gene (glnK) in a ribulose bisphosphate carboxylase/oxygenase-deficient mutant of Rhodobacter sphaeroides.

作者信息

Qian Y, Tabita F R

机构信息

The Biochemistry Program and The, The Ohio State University, Columbus, Ohio 43210-1292, USA.

出版信息

J Bacteriol. 1998 Sep;180(17):4644-9. doi: 10.1128/JB.180.17.4644-4649.1998.

Abstract

In a ribulose 1,5-bisphosphate carboxylase/oxygenase (RubisCO)-deficient mutant of Rhodobacter sphaeroides, strain 16PHC, nitrogenase activity was derepressed in the presence of ammonia under photoheterotrophic growth conditions. Previous studies also showed that reintroduction of a functional RubisCO and Calvin-Benson-Bassham (CBB) pathway suppressed the deregulation of nitrogenase synthesis in this strain. In this study, the derepression of nitrogenase synthesis in the presence of ammonia in strain 16PHC was further explored by using a glnB::lacZ fusion, since the product of the glnB gene is known to have a negative effect on ammonia-regulated nif control. It was found that glnB expression was repressed in strain 16PHC under photoheterotrophic growth conditions with either ammonia or glutamate as the nitrogen source; glutamine synthetase (GS) levels were also affected in this strain. However, when cells regained a functional CBB pathway by trans complementation of the deleted genes, wild-type levels of GS and glnB expression were restored. Furthermore, a glnB-like gene, glnK, was isolated from this organism, and its expression was found to be under tight nitrogen control in the wild type. Surprisingly, glnK expression was found to be derepressed in strain 16PHC under photoheterotrophic conditions in the presence of ammonia.

摘要

在球形红细菌(Rhodobacter sphaeroides)的1,5-二磷酸核酮糖羧化酶/加氧酶(RubisCO)缺陷型突变体菌株16PHC中,在光异养生长条件下,氨的存在会使固氮酶活性去阻遏。先前的研究还表明,重新引入功能性RubisCO和卡尔文-本森-巴斯姆(CBB)途径可抑制该菌株中固氮酶合成的失调。在本研究中,通过使用glnB::lacZ融合来进一步探究菌株16PHC中氨存在时固氮酶合成的去阻遏情况,因为已知glnB基因的产物对氨调节的nif控制有负面影响。研究发现,在以氨或谷氨酸作为氮源的光异养生长条件下,菌株16PHC中的glnB表达受到抑制;该菌株中的谷氨酰胺合成酶(GS)水平也受到影响。然而,当细胞通过对缺失基因的反式互补重新获得功能性CBB途径时,GS和glnB表达恢复到野生型水平。此外,从该生物体中分离出一个类似glnB的基因glnK,发现其表达在野生型中受到严格的氮控制。令人惊讶的是,发现在光异养条件下氨存在时,菌株16PHC中的glnK表达去阻遏。

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