Isolation of state transition mutants of Chlamydomonas reinhardtii by fluorescence video imaging

被引:41
作者
Kruse, O [1 ]
Nixon, PJ
Schmid, GH
Mullineaux, CW
机构
[1] Univ Bielefeld, Dept Biol, D-33501 Bielefeld, Germany
[2] Univ London Imperial Coll Sci Technol & Med, Dept Biochem, London SW7 2AZ, England
[3] UCL, Dept Biol, London WC1E 6BT, England
关键词
Chlamydomonas reinhardtii; LHC II phosphorylation; mutagenesis; Photosystem II redox control; state 2 to state 1 transition; transformation;
D O I
10.1023/A:1006229308606
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Oxygenic photosynthetic organisms adapt to varying light conditions by changing the distribution of light energy between Photosystem II (PS II) and photosystem I (PS I) during so-called state transitions. To identify the genes involved in this process, we have exploited a simple chlorophyll fluorescence video-imaging technique to screen a library of nuclear mutants of Chlamydomonas reinhardtii for colonies grown on agar plates that are disturbed in their ability to regulate light energy distribution between PS I and PS II. Subsequent modulated fluorescence measurements at room temperature and 77 K fluorescence emission spectra confirmed that 5 mutants (0.025% of total number screened) were defective in state transitions. [(32)P]orthophosphate phosphorylation experiments in vivo revealed that in one of these mutants, designated stm1, the level of LHC II polypeptide phosphorylation was drastically reduced compared with wild type. Despite WT levels of PS I and PS II, stm1 grew photoautotrophically at reduced rates, compared with WT especially under low light conditions, which is consistent with an important physiological role for state transitions. Our results highlight the feasibility of video imaging in tandem with mutagenesis as a means of identifying the genes involved in controlling state transitions in eukaryotic photosynthetic organisms.
引用
收藏
页码:43 / 51
页数:9
相关论文
共 38 条
[11]   CYTOCHROME-B6F COMPLEX IS REQUIRED FOR PHOSPHORYLATION OF LIGHT-HARVESTING CHLOROPHYLL A/B COMPLEX-II IN CHLOROPLAST PHOTOSYNTHETIC MEMBRANES [J].
BENNETT, J ;
SHAW, EK ;
MICHEL, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 171 (1-2) :95-100
[12]   PROTEIN-PHOSPHORYLATION IN GREEN PLANT CHLOROPLASTS [J].
BENNETT, J .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1991, 42 :281-311
[13]  
BOICHENKO VA, 1994, PHOTOSYNTHETICA, V30, P527
[14]  
Boichenko VA, 1998, BIOCHEMISTRY-MOSCOW+, V63, P164
[15]   Phosphatase activities in spinach thylakoid membranes - Effectors, regulation and location [J].
Carlberg, I ;
Andersson, B .
PHOTOSYNTHESIS RESEARCH, 1996, 47 (02) :145-156
[16]  
COUGHLAN SJ, 1986, J BIOL CHEM, V261, P1378
[17]   THE ARGININOSUCCINATE LYASE GENE OF CHLAMYDOMONAS-REINHARDTII - AN IMPORTANT TOOL FOR NUCLEAR TRANSFORMATION AND FOR CORRELATING THE GENETIC AND MOLECULAR MAPS OF THE ARG7 LOCUS [J].
DEBUCHY, R ;
PURTON, S ;
ROCHAIX, JD .
EMBO JOURNAL, 1989, 8 (10) :2803-2809
[18]   ISOLATION OF HIGHLY-ACTIVE PHOTOSYSTEM-II PARTICLES FROM A MUTANT OF CHLAMYDOMONAS-REINHARDTII [J].
DINER, BA ;
WOLLMAN, FA .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1980, 110 (02) :521-526
[19]  
EHLICH TD, 1992, PROTEIN J BIOL CHEM, V267, P3523
[20]  
EMLYNJONES D, 1999, UNPUB GENE REQUIRED