Cloning and expression of the tobacco CHLM sequence encoding Mg protoporphyrin IX methyltransferase and its interaction with Mg chelatase

被引:42
作者
Alawady, A
Reski, R
Yaronskaya, E
Grimm, B
机构
[1] Humboldt Univ, Inst Biol Pflanzenphysiol, D-10115 Berlin, Germany
[2] Univ Freiburg, D-79104 Freiburg, Germany
[3] Natl Acad Sci Belarus, Inst Biophys & Cell Engn, Minsk 220072, BELARUS
关键词
chlorophyll; chloroplast development; photosynthesis; tetrapyrrole;
D O I
10.1007/s11103-005-1427-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
S-adenosyl-L-methionine:Mg-protoporphyrin IX methyltransferase (MgPMT) is an enzyme in the Mg branch of the tetrapyrrole biosynthetic pathway. The nucleotide sequence of tobacco (Nicotiana tabacum) CHLM was identified and the cDNA sequence was used to express the precursor, the mature and a truncated recombinant MgPMT for enzymatic activity tests and for the formation of polyclonal antibodies. Comparison of the mature and the truncated MgPMT revealed three critical amino acids at the N-terminus of MgPMT for the maintenance of enzyme activity. To assess the contribution of CHLM expression to the control of the metabolic flow in the tetrapyrrole pathway, CHLM transcripts and protein levels, the enzyme activity and the steady-state levels of Mg protoporphyrin and Mg protoporphyrin monomethylester were analysed during greening of seedlings and plant development as well as under day/night and continuous growth conditions. These expression studies revealed posttranslational activation of MgPMT during greening and light/dark-cycles. Using the yeast two-hybrid system physical interaction was demonstrated between MgPMT and the CHLH subunit of Mg chelatase. Activity of recombinant MgPMT expressed in yeast cells was stimulated in the presence of the recombinant CHLH subunit. Implications for posttranslational regulation of MgPMT are discussed for the enzymatic steps at the beginning of the Mg branch.
引用
收藏
页码:679 / 691
页数:13
相关论文
共 40 条
[1]   Tobacco Mg protoporphyrin IX methyltransferase is involved in inverse activation of Mg porphyrin and protoheme synthesis [J].
Alawady, AE ;
Grimm, B .
PLANT JOURNAL, 2005, 41 (02) :282-290
[2]  
[Anonymous], 1997, EMBnet News
[3]   Enzymes of chlorophyll biosynthesis [J].
Beale, SI .
PHOTOSYNTHESIS RESEARCH, 1999, 60 (01) :43-73
[4]   THE CIRCADIAN OSCILLATOR COORDINATES THE SYNTHESIS OF APOPROTEINS AND THEIR PIGMENTS DURING CHLOROPLAST DEVELOPMENT [J].
BEATOR, J ;
KLOPPSTECH, K .
PLANT PHYSIOLOGY, 1993, 103 (01) :191-196
[5]   The plant S-adenosyl-L-methionine:Mg-protoporphyrin IX methyltransferase is located in both envelope and thylakoid chloroplast membranes [J].
Block, MA ;
Tewari, AK ;
Albrieux, C ;
Maréchal, E ;
Joyard, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2002, 269 (01) :240-248
[6]   DIRECTED MUTATIONAL ANALYSIS OF BACTERIOCHLOROPHYLL-ALPHA BIOSYNTHESIS IN RHODOBACTER-CAPSULATUS [J].
BOLLIVAR, DW ;
SUZUKI, JY ;
BEATTY, JT ;
DOBROWOLSKI, JM ;
BAUER, CE .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 237 (05) :622-640
[7]   REGULATION OF THE YEAST HO GENE [J].
BREEDEN, L ;
NASMYTH, K .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1985, 50 :643-650
[8]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[9]  
EBBON J, 1969, STUDIES S ADENOSYLME, V111, P573
[10]   Predicting subcellular localization of proteins based on their N-terminal amino acid sequence [J].
Emanuelsson, O ;
Nielsen, H ;
Brunak, S ;
von Heijne, G .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (04) :1005-1016