Ho Ming-Yang, Gan Fei, Shen Gaozhong, Zhao Chi, Bryant Donald A
403C Althouse Laboratory, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, 16802, USA.
Intercollege Graduate Degree Program in Plant Biology, The Pennsylvania State University, University Park, PA, 16802, USA.
Photosynth Res. 2017 Feb;131(2):173-186. doi: 10.1007/s11120-016-0309-z. Epub 2016 Sep 16.
Far-red light photoacclimation (FaRLiP) is a mechanism that allows some cyanobacteria to utilize far-red light (FRL) for oxygenic photosynthesis. During FaRLiP, cyanobacteria remodel photosystem (PS) I, PS II, and phycobilisomes while synthesizing Chl d, Chl f, and far-red-absorbing phycobiliproteins, and these changes enable these organisms to use FRL for growth. In this study, a conjugation-based genetic system was developed for Synechococcus sp. PCC 7335. Three antibiotic cassettes were successfully used to generate knockout mutations in genes in Synechococcus sp. PCC 7335, which should allow up to three gene loci to be modified in one strain. This system was used to delete the rfpA, rfpB, and rfpC genes individually, and characterization of the mutants demonstrated that these genes control the expression of the FaRLiP gene cluster in Synechococcus sp. PCC 7335. The mutant strains exhibited some surprising differences from similar mutants in other FaRLiP strains. Notably, mutations in any of the three master transcription regulatory genes led to enhanced synthesis of phycocyanin and PS II. A time-course study showed that acclimation of the photosynthetic apparatus from that produced in white light to that produced in FRL occurs very slowly over a period 12-14 days in this strain and that it is associated with a substantial reduction (~34 %) in the chlorophyll a content of the cells. This study shows that there are differences in the detailed responses of cyanobacteria to growth in FRL in spite of the obvious similarities in the organization and regulation of the FaRLiP gene cluster.
远红光光适应(FaRLiP)是一种使某些蓝细菌能够利用远红光(FRL)进行产氧光合作用的机制。在FaRLiP过程中,蓝细菌在合成叶绿素d、叶绿素f和吸收远红光的藻胆蛋白的同时,对光系统(PS)I、PS II和藻胆体进行重塑,这些变化使这些生物体能够利用FRL进行生长。在本研究中,为聚球藻属PCC 7335开发了一种基于接合的遗传系统。三个抗生素盒成功用于在聚球藻属PCC 7335的基因中产生敲除突变,这应该允许在一个菌株中最多修饰三个基因座。该系统用于分别删除rfpA、rfpB和rfpC基因,对突变体的表征表明这些基因控制聚球藻属PCC 7335中FaRLiP基因簇的表达。突变菌株与其他FaRLiP菌株中的类似突变体表现出一些惊人的差异。值得注意的是,三个主要转录调控基因中任何一个的突变都会导致藻蓝蛋白和PS II的合成增强。一项时间进程研究表明,在该菌株中,光合装置从白光下产生的光合装置适应到FRL下产生的光合装置的过程在12 - 14天的时间内非常缓慢地发生,并且这与细胞叶绿素a含量的大幅降低(约34%)相关。这项研究表明,尽管FaRLiP基因簇的组织和调控存在明显相似性,但蓝细菌对FRL生长的详细反应存在差异。