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Identification and organization of carbon dioxide fixation genes in Xanthobacter flavus H4-14.

作者信息

Meijer W G, Arnberg A C, Enequist H G, Terpstra P, Lidstrom M E, Dijkhuizen L

机构信息

Department of Microbiology, University of Groningen, The Netherlands.

出版信息

Mol Gen Genet. 1991 Feb;225(2):320-30. doi: 10.1007/BF00269865.

DOI:10.1007/BF00269865
PMID:1900916
Abstract

The genes encoding the large (cfxL) and small (cfxS) subunits of ribulose-1,5-bisphosphate carboxylase (RuBisC/O) from Xanthobacter flavus H4-14 were identified and characterized. The RuBisC/O genes are separated by 11 bp and cotranscribed in Escherichia coli from the lac promoter in the order cfxLS. Primer extension and R-loop experiments with RNA isolated from autotrophically grown X. flavus H4-14 showed that transcription of cfxL and cfxS initiated 22 bp upstream from cfxL and resulted in a mRNA of at least 2.3 kb. DNA sequence analysis identified the start of an open reading frame transcribed divergently from cfxL, and displaying significant similarities with genes belonging to the lysR family of transcriptional activators. Downstream from cfxS an additional open reading frame was identified with unknown function. Expression studies showed that the genes encoding fructosebisphosphatase (cfxF) and phosphoribulokinase (cfxP) are located downstream from cfxLS. The cfxF and cfxP genes are cotranscribed in the same direction as cfxLS in the order cfxFP.

摘要

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本文引用的文献

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Molecular cloning and sequence analysis of the cyanobacterial gene for the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase.藻蓝细菌核酮糖-1,5-二磷酸羧化酶/加氧酶大亚基基因的分子克隆和序列分析。
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A site-specific mutation within the active site of ribulose-1,5-bisphosphate carboxylase of Rhodospirillum rubrum.
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