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Isolation and Characterization of a Mutant of Chlamydomonas reinhardtii Deficient in the CO(2) Concentrating Mechanism.莱茵衣藻突变体的分离与鉴定,该突变体缺乏 CO2 浓缩机制。
Plant Physiol. 1989 Mar;89(3):897-903. doi: 10.1104/pp.89.3.897.
2
Adaptation to CO(2) Level and Changes in the Phosphorylation of Thylakoid Proteins during the Cell Cycle of Chlamydomonas reinhardtii.莱茵衣藻细胞周期中对二氧化碳水平的适应及类囊体蛋白磷酸化的变化
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Internal Inorganic Carbon Pool of Chlamydomonas reinhardtii: EVIDENCE FOR A CARBON DIOXIDE-CONCENTRATING MECHANISM.莱茵衣藻的体内无机碳库:二氧化碳浓缩机制的证据。
Plant Physiol. 1980 Sep;66(3):407-13. doi: 10.1104/pp.66.3.407.
4
CO2 CONCENTRATING MECHANISMS IN PHOTOSYNTHETIC MICROORGANISMS.光合微生物中的二氧化碳浓缩机制
Annu Rev Plant Physiol Plant Mol Biol. 1999 Jun;50:539-570. doi: 10.1146/annurev.arplant.50.1.539.
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A New Screening Method for Algal Photosynthetic Mutants (CO2-Insensitive Mutants of the Green Alga Chlorella ellipsoidea).一种用于藻类光合突变体(椭圆小球藻的二氧化碳不敏感突变体)的新筛选方法。
Plant Physiol. 1996 Apr;110(4):1283-1291. doi: 10.1104/pp.110.4.1283.
6
Generation of expressed sequence tags from low-CO2 and high-CO2 adapted cells of Chlamydomonas reinhardtii.从莱茵衣藻适应低二氧化碳和高二氧化碳的细胞中生成表达序列标签。
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7
The Crd1 gene encodes a putative di-iron enzyme required for photosystem I accumulation in copper deficiency and hypoxia in Chlamydomonas reinhardtii.Crd1基因编码一种假定的双铁酶,该酶是莱茵衣藻在铜缺乏和缺氧条件下光系统I积累所必需的。
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8
Psr1, a nuclear localized protein that regulates phosphorus metabolism in Chlamydomonas.Psr1,一种定位于细胞核的蛋白质,可调节衣藻中的磷代谢。
Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):15336-41. doi: 10.1073/pnas.96.26.15336.
9
CO(2)-responsive transcriptional regulation of CAH1 encoding carbonic anhydrase is mediated by enhancer and silencer regions in Chlamydomonas reinhardtii.莱茵衣藻中编码碳酸酐酶的CAH1的二氧化碳响应转录调控由增强子和沉默子区域介导。
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10
As Chlamydomonas reinhardtii acclimates to low-CO2 conditions there is an increase in cyclophilin expression.随着莱茵衣藻适应低二氧化碳条件,亲环蛋白的表达会增加。
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Ccm1是一种调控基因,通过感知二氧化碳的可利用性来控制莱茵衣藻中碳浓缩机制的诱导。

Ccm1, a regulatory gene controlling the induction of a carbon-concentrating mechanism in Chlamydomonas reinhardtii by sensing CO2 availability.

作者信息

Fukuzawa H, Miura K, Ishizaki K, Kucho K I, Saito T, Kohinata T, Ohyama K

机构信息

Division of Integrated Life Science, Graduate School of Biostudies, Kyoto University, Kyoto 606-8502, Japan.

出版信息

Proc Natl Acad Sci U S A. 2001 Apr 24;98(9):5347-52. doi: 10.1073/pnas.081593498. Epub 2001 Apr 3.

DOI:10.1073/pnas.081593498
PMID:11287669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC33212/
Abstract

Aquatic photosynthetic organisms, including the green alga Chlamydomonas reinhardtii, induce a set of genes for a carbon-concentrating mechanism (CCM) to acclimate to CO2-limiting conditions. This acclimation is modulated by some mechanisms in the cell to sense CO2 availability. Previously, a high-CO2-requiring mutant C16 defective in an induction of the CCM was isolated from C. reinhardtii by gene tagging. By using this pleiotropic mutant, we isolated a nuclear regulatory gene, Ccm1, encoding a 699-aa hydrophilic protein with a putative zinc-finger motif in its N-terminal region and a Gln repeat characteristic of transcriptional activators. Introduction of Ccm1 into this mutant restored an active carbon transport through the CCM, development of a pyrenoid structure in the chloroplast, and induction of a set of CCM-related genes. That a 5,128-base Ccm1 transcript and also the translation product of 76 kDa were detected in both high- and low-CO2 conditions suggests that CCM1 might be modified posttranslationally. These data indicate that Ccm1 is essential to control the induction of CCM by sensing CO2 availability in Chlamydomonas cells. In addition, complementation assay and identification of the mutation site of another pleiotropic mutant, cia5, revealed that His-54 within the putative zinc-finger motif of the CCM1 is crucial to its regulatory function.

摘要

包括绿藻莱茵衣藻在内的水生光合生物会诱导一套碳浓缩机制(CCM)相关基因,以适应二氧化碳限制条件。这种适应性由细胞内的一些机制调节,以感知二氧化碳的可利用性。此前,通过基因标签从莱茵衣藻中分离出了一个在CCM诱导方面存在缺陷的高二氧化碳需求突变体C16。利用这个多效性突变体,我们分离出了一个核调节基因Ccm1,它编码一种699个氨基酸的亲水性蛋白质,在其N端区域具有一个推定的锌指基序和转录激活因子特有的谷氨酰胺重复序列。将Ccm1导入该突变体可恢复通过CCM的活跃碳转运、叶绿体中淀粉核结构的发育以及一组CCM相关基因的诱导。在高二氧化碳和低二氧化碳条件下都检测到了5128个碱基的Ccm1转录本以及76 kDa的翻译产物,这表明CCM1可能在翻译后被修饰。这些数据表明,Ccm1对于通过感知莱茵衣藻细胞中的二氧化碳可利用性来控制CCM的诱导至关重要。此外,对另一个多效性突变体cia5的互补分析和突变位点鉴定表明,CCM1推定锌指基序内的His-54对其调节功能至关重要。