Böhnke Stefanie, Perner Mirjam
Molecular Biology of Microbial Consortia, Biocenter Klein Flottbek, University of HamburgHamburg, Germany.
Front Microbiol. 2017 Jul 12;8:1303. doi: 10.3389/fmicb.2017.01303. eCollection 2017.
Ribulose-1,5-bisphosphate carboxylase/oxygenase (RubisCO) catalyzes the first major step of carbon fixation in the Calvin-Benson-Bassham (CBB) cycle. This autotrophic CO fixation cycle accounts for almost all the assimilated carbon on Earth. Due to the primary role that RubisCO plays in autotrophic carbon fixation, it is important to understand how its gene expression is regulated and the enzyme is activated. Since the majority of all microorganisms are currently not culturable, we used a metagenomic approach to identify genes and enzymes associated with RubisCO expression. The investigated metagenomic DNA fragment originates from the deep-sea hydrothermal vent field Nibelungen at 8°18' S along the Mid-Atlantic Ridge. It is 13,046 bp and resembles genes from . The fragment encodes nine open reading frames (ORFs) which include two types of RubisCO, form I (CbbL/S) and form II (CbbM), two LysR transcriptional regulators (LysR1 and LysR2), two von Willebrand factor type A (CbbO-m and CbbO-1), and two AAA+ ATPases (CbbQ-m and CbbQ-1), expected to function as RubisCO activating enzymes. analyses uncovered several putative LysR binding sites and promoter structures. Functions of some of these DNA motifs were experimentally confirmed. For example, according to mobility shift assays LysR1's binding ability to the intergenic region of and appears to be intensified when CbbL or LysR2 are present. Binding of LysR2 upstream of appears to be intensified if CbbM is present. Our study suggests that CbbQ-m and CbbO-m activate CbbL and that LysR1 and LysR2 proteins promote CbbQ-m/CbbO-m expression. CbbO-1 seems to activate CbbM and CbbM itself appears to contribute to intensifying LysR's binding ability and thus its own transcriptional regulation. CbbM furthermore appears to impair expression. A model summarizes the findings and predicts putative interactions of the different proteins influencing RubisCO gene regulation and expression.
1,5 - 二磷酸核酮糖羧化酶/加氧酶(RubisCO)催化卡尔文 - 本森 - 巴斯姆(CBB)循环中碳固定的第一步主要反应。这个自养型二氧化碳固定循环几乎占了地球上所有同化碳的来源。由于RubisCO在自养型碳固定中起主要作用,了解其基因表达如何调控以及该酶如何被激活很重要。鉴于目前大多数微生物无法培养,我们采用宏基因组学方法来鉴定与RubisCO表达相关的基因和酶。所研究的宏基因组DNA片段来自中大西洋海岭南纬8°18′处的深海热液喷口区域尼伯龙根。它有13046个碱基对,与来自……的基因相似。该片段编码9个开放阅读框(ORF),包括两种类型的RubisCO,即I型(CbbL/S)和II型(CbbM),两个LysR转录调节因子(LysR1和LysR2),两个血管性血友病因子A(CbbO - m和CbbO - 1),以及两个AAA + ATP酶(CbbQ - m和CbbQ - 1),预计它们作为RubisCO激活酶发挥作用。分析发现了几个假定的LysR结合位点和启动子结构。其中一些DNA基序的功能已通过实验得到证实。例如,根据凝胶迁移实验,当存在CbbL或LysR2时,LysR1与……基因间区域的结合能力似乎增强。如果存在CbbM,LysR2在……上游的结合似乎增强。我们的研究表明,CbbQ - m和CbbO - m激活CbbL,并且LysR1和LysR2蛋白促进CbbQ - m/CbbO - m的表达。CbbO - 1似乎激活CbbM,并且CbbM本身似乎有助于增强LysR的结合能力,从而促进其自身的转录调控。此外,CbbM似乎会损害……的表达。一个模型总结了这些发现,并预测了影响RubisCO基因调控和表达的不同蛋白质之间的假定相互作用。