Meijer W G
Department of Microbiology, University of Groningen, Haren, The Netherlands.
J Bacteriol. 1994 Oct;176(19):6120-6. doi: 10.1128/jb.176.19.6120-6126.1994.
During autotrophic growth of Xanthobacter flavus, energy derived from the oxidation of hydrogen methanol or formate is used to drive the assimilation of CO2 via the Calvin cycle. The genes encoding the Calvin cycle enzymes are organized in the cbb operon, which is expressed only during autotrophic growth. Although it has been established that the transcriptional activator CbbR is required for the expression of the cbb operon, it is unclear whether CbbR is the only factor contributing to the regulation of the cbb operon. This paper describes the isolation of X. flavus mutants which were affected in the regulation of the cbb operon. One of the mutant strains was subject to an enhanced repression of the cbb operon promoter by the gluconeogenic substrate succinate and in addition failed to grow autotrophically. The rate of growth of the X. flavus mutant on succinate-containing medium was lower than that of the wild-type strain, but rates of growth on medium supplemented with gluconate were identical. A genomic library of X. flavus was constructed and was used to complement the mutant strain. The nucleotide sequence of the DNA fragment required to restore autotrophic growth of the X. flavus mutant was determined. One open reading frame that displayed extensive similarities to phosphoglycerate kinase-encoding genes (pgk) was identified. The X. flavus mutant lacked phosphoglycerate kinase activity following growth on gluconate or succinate. Introduction of the pgk gene into the X. flavus mutant partially restored the activity of phosphoglycerate kinase. Induction of the cbb operon of the X. flavus wild-type strain resulted in a simultaneous and parallel increase in the activities of ribulose-1,5-biphosphate carboxylase and phosphoglycerate kinase, whereas the latter activity remained absent in the X. flavus pgk mutant. It is concluded that X. flavus employees a single phosphoglycerate kinase enzyme and this is not encoded within the cbb operon.
在黄杆菌自养生长过程中,由氢气、甲醇或甲酸氧化产生的能量用于驱动卡尔文循环以同化二氧化碳。编码卡尔文循环酶的基因组织在cbb操纵子中,该操纵子仅在自养生长期间表达。虽然已经确定转录激活因子CbbR是cbb操纵子表达所必需的,但尚不清楚CbbR是否是唯一参与cbb操纵子调控的因子。本文描述了在cbb操纵子调控方面受到影响的黄杆菌突变体的分离。其中一个突变菌株受到糖异生底物琥珀酸对cbb操纵子启动子的增强抑制,并且此外无法进行自养生长。黄杆菌突变体在含琥珀酸培养基上的生长速率低于野生型菌株,但在补充葡萄糖酸盐的培养基上的生长速率相同。构建了黄杆菌的基因组文库并用于互补突变菌株。确定了恢复黄杆菌突变体自养生长所需的DNA片段的核苷酸序列。鉴定出一个与磷酸甘油酸激酶编码基因(pgk)具有广泛相似性的开放阅读框。在葡萄糖酸盐或琥珀酸上生长后,黄杆菌突变体缺乏磷酸甘油酸激酶活性。将pgk基因导入黄杆菌突变体中部分恢复了磷酸甘油酸激酶的活性。黄杆菌野生型菌株的cbb操纵子的诱导导致1,5-二磷酸核酮糖羧化酶和磷酸甘油酸激酶的活性同时平行增加,而在黄杆菌pgk突变体中后者活性仍然不存在。得出的结论是,黄杆菌使用单一的磷酸甘油酸激酶酶,并且该酶不在cbb操纵子内编码。