Klanchui Amornpan, Cheevadhanarak Supapon, Prommeenate Peerada, Meechai Asawin
Biological Engineering Program, Faculty of Engineering, King Mongkut's University of Technology Thonburi, Bangkok 10140, Thailand.
Division of Biotechnology, School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok 10150, Thailand.
Comput Struct Biotechnol J. 2017 May 25;15:340-350. doi: 10.1016/j.csbj.2017.05.001. eCollection 2017.
In cyanobacteria, the CO-concentrating mechanism (CCM) is a vital biological process that provides effective photosynthetic CO fixation by elevating the CO level near the active site of Rubisco. This process enables the adaptation of cyanobacteria to various habitats, particularly in CO-limited environments. Although CCM of freshwater and marine cyanobacteria are well studied, there is limited information on the CCM of cyanobacteria living under alkaline environments. Here, we aimed to explore the molecular components of CCM in 12 alkaliphilic cyanobacteria through genome-based analysis. These cyanobacteria included 6 moderate alkaliphiles; sp. PCC 7327, spp., spp., PCC 9445, and 6 strong alkaliphiles (i.e. spp.). The results showed that both groups belong to β-cyanobacteria based on β-carboxysome shell proteins with form 1B of Rubisco. They also contained standard genes, cluster, which is essential for β-carboxysome formation. Most strains did not have the high-affinity Na/HCO symporter SbtA and the medium-affinity ATP-dependent HCO transporter BCT1. Specifically, all strong alkaliphiles appeared to lack BCT1. Beside the transport systems, carboxysomal β-CA, CcaA, was absent in all alkaliphiles, except for three moderate alkaliphiles: sp. PCC 7327, PCC 7202, and PCC 9445. Furthermore, comparative analysis of the CCM components among freshwater, marine, and alkaliphilic β-cyanobacteria revealed that the basic molecular components of the CCM in the alkaliphilic cyanobacteria seemed to share more degrees of similarity with freshwater than marine cyanobacteria. These findings provide a relationship between the CCM components of cyanobacteria and their habitats.
在蓝细菌中,CO2浓缩机制(CCM)是一个至关重要的生物学过程,它通过提高核酮糖-1,5-二磷酸羧化酶(Rubisco)活性位点附近的CO2水平来实现有效的光合CO2固定。这一过程使蓝细菌能够适应各种生境,尤其是在CO2受限的环境中。尽管淡水和海洋蓝细菌的CCM已得到充分研究,但关于生活在碱性环境中的蓝细菌的CCM信息有限。在此,我们旨在通过基于基因组的分析来探索12种嗜碱蓝细菌中CCM的分子成分。这些蓝细菌包括6种中度嗜碱菌,即sp. PCC 7327、 spp.、 spp.、PCC 9445,以及6种强碱嗜菌(即 spp.)。结果表明,基于具有Rubisco 1B形式的β-羧酶体外壳蛋白,这两组均属于β-蓝细菌。它们还含有对β-羧酶体形成至关重要的标准基因cluster。大多数菌株没有高亲和力的Na+/HCO3-同向转运蛋白SbtA和中等亲和力的ATP依赖性HCO3-转运蛋白BCT1。具体而言,所有强碱嗜菌似乎都缺乏BCT1。除了转运系统外,除了三种中度嗜碱菌sp. PCC 7327、PCC 7202和PCC 9445外,所有嗜碱菌中均不存在羧酶体β-碳酸酐酶(CcaA)。此外,对淡水、海洋和嗜碱β-蓝细菌中CCM成分的比较分析表明,嗜碱蓝细菌中CCM的基本分子成分与淡水蓝细菌的相似程度似乎高于与海洋蓝细菌的相似程度。这些发现揭示了蓝细菌CCM成分与其生境之间的关系。