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丝状蓝细菌鱼腥藻Anabaena sp. PCC 7120光合天线缺陷突变体的表征及对环境信号的响应

Characterization and responses to environmental cues of a photosynthetic antenna-deficient mutant of the filamentous cyanobacterium Anabaena sp. PCC 7120.

作者信息

Leganés Francisco, Martínez-Granero Francisco, Muñoz-Martín M Ángeles, Marco Eduardo, Jorge Alberto, Carvajal Laura, Vida Teresa, González-Pleiter Miguel, Fernández-Piñas Francisca

机构信息

Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049, Spain.

Departamento de Biología, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049, Spain.

出版信息

J Plant Physiol. 2014 Jul 1;171(11):915-26. doi: 10.1016/j.jplph.2014.03.005. Epub 2014 Mar 28.

DOI:10.1016/j.jplph.2014.03.005
PMID:24913049
Abstract

The cyanobacterial phycobilisome (PBS) is a giant pigment-protein complex which harvests light energy for photosynthesis and comprises two structures: a core and peripheral rods. Most studies on PBS structure and function are based on mutants of unicellular strains. In this report, we describe the phenotypic and genetic characterization of a transposon mutant of the filamentous Anabaena sp. strain PCC 7120, denoted LC1, which cannot synthesize the phycobiliprotein phycocyanin (PC), the main component of the rods; in this mutant, the transposon had inserted into the cpcB gene (orf alr0528) which putatively encodes PC-β chain. Mutant LC1 was able to synthesize phycoerythrocyanin (PEC), a phycobiliprotein (PBP) located at the terminal region of the rods; but in the absence of PC, PEC did not attach to the PBSs that only retained the allophycocyanin (APC) core; ferredoxin: NADP+-oxidoreductase (FNR) that is associated with the PBS in the wild type, was not found in isolated PBSs from LC1. The performance of the mutant exposed to different environmental conditions was evaluated. The mutant phenotype was successfully complemented by cloning and transfer of the wild type complete cpc operon to mutant LC1. Interestingly, LC1 compensated its mutation by significantly increasing the number of its core-PBS and the effective quantum yield of photosystem II (PSII) photochemistry; this feature suggests a more efficient energy conversion in the mutant which may be useful for biotechnological applications.

摘要

蓝藻藻胆体(PBS)是一种巨大的色素 - 蛋白质复合体,它为光合作用收集光能,由核心和外周棒状结构组成。大多数关于PBS结构和功能的研究基于单细胞菌株的突变体。在本报告中,我们描述了丝状鱼腥藻Anabaena sp. 菌株PCC 7120的一个转座子突变体的表型和遗传特征,该突变体命名为LC1,它不能合成藻胆蛋白藻蓝蛋白(PC),PC是外周棒状结构的主要成分;在这个突变体中,转座子插入到了可能编码PC - β链的cpcB基因(orf alr0528)中。突变体LC1能够合成藻红蓝蛋白(PEC),一种位于外周棒状结构末端区域的藻胆蛋白(PBP);但是在没有PC的情况下,PEC没有附着到仅保留别藻蓝蛋白(APC)核心的PBS上;在野生型中与PBS相关的铁氧还蛋白:NADP⁺ - 氧化还原酶(FNR),在从LC1分离的PBS中未发现。评估了该突变体在不同环境条件下的表现。通过将野生型完整的cpc操纵子克隆并转移到突变体LC1中,成功互补了突变体表型。有趣的是,LC1通过显著增加其核心PBS的数量和光系统II(PSII)光化学的有效量子产率来补偿其突变;这一特征表明突变体中能量转换更高效,这可能对生物技术应用有用。

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