Regulation of secondary metabolism by the carbon-nitrogen status in tobacco: nitrate inhibits large sectors of phenylpropanoid metabolism

被引:287
作者
Fritz, C
Palacios-Rojas, N
Feil, R
Stitt, M
机构
[1] Max Planck Inst Mol Plant Physiol, Dept 2, D-14476 Golm, Germany
[2] CIMMYT, Mexico City 06600, DF, Mexico
关键词
carbon-nutrient hypothesis; nicotine; nitrate; nitrate reductase; phenylpropanopids; secondary metabolism;
D O I
10.1111/j.1365-313X.2006.02715.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Interactions between nitrogen and carbon metabolism modulate many aspects of the metabolism, physiology and development of plants. This paper investigates the contribution of nitrate and nitrogen metabolism to the regulation of phenylpropanoid and nicotine synthesis. Wild-type tobacco was grown on 12 or 0.2 mM nitrate and compared with a nitrate reductase-deficient mutant [Nia30(145)] growing on 12 mM nitrate. Nitrate-deficient wild-type plants accumulate high levels of a range of phenylpropanoids including chlorogenic acid, contain high levels of rutin, are highly lignified, but contain less nicotine than nitrogen-replete wild-type tobacco. Nia30( 145) resembles nitrate-deficient wild-type plants with respect to the levels of amino acids, but accumulates large amounts of nitrate. The levels of phenylpropanoids, rutin and lignin resemble those in nitrogen-replete wild-type plants, whereas the level of nicotine resembles that in nitrate-deficient wild-type plants. Expression arrays and real time RT-PCR revealed that a set of genes required for phenylpropanoid metabolism including PAL, 4CL and HQT are induced in nitrogen-deficient wild-type plants but not in Nia30( 145). It is concluded that nitrogen deficiency leads to a marked shift from the nitrogen-containing alkaloid nicotine to carbon-rich phenylpropanoids. The stimulation of phenylpropanoid metabolism is triggered by changes of nitrate, rather than downstream nitrogen metabolites, and is mediated by induction of a set of enzymes in the early steps of the phenylpropanoid biosynthetic pathway.
引用
收藏
页码:533 / 548
页数:16
相关论文
共 62 条
[51]  
Tosserams Marcel, 2001, Plant Ecology, V154, P159
[52]  
Turpin D., 1997, Plant Metabolism, P509
[53]   Extension of the visualization tool MapMan to allow statistical analysis of arrays, display of coresponding genes, and comparison with known responses [J].
Usadel, B ;
Nagel, A ;
Thimm, O ;
Redestig, H ;
Blaesing, OE ;
Palacios-Rojas, N ;
Selbig, J ;
Hannemann, J ;
Piques, MC ;
Steinhauser, D ;
Scheible, WR ;
Gibon, Y ;
Morcuende, R ;
Weicht, D ;
Meyer, S ;
Stitt, M .
PLANT PHYSIOLOGY, 2005, 138 (03) :1195-1204
[54]  
VanDam NM, 1996, FUNCT ECOL, V10, P128, DOI 10.2307/2390271
[55]  
VANDERWERF A, 1993, PHYSIOL PLANTARUM, V89, P563, DOI 10.1111/j.1399-3054.1993.tb05214.x
[56]   FUNCTIONAL COMPLEMENTATION OF TOBACCO AND NICOTIANA-PLUMBAGINIFOLIA NITRATE REDUCTASE DEFICIENT MUTANTS BY TRANSFORMATION WITH THE WILD-TYPE ALLELES OF THE TOBACCO STRUCTURAL GENES [J].
VAUCHERET, H ;
CHABAUD, M ;
KRONENBERGER, J ;
CABOCHE, M .
MOLECULAR & GENERAL GENETICS, 1990, 220 (03) :468-474
[57]   Signaling mechanisms integrating root and shoot responses to changes in the nitrogen supply [J].
Walch-Liu, P ;
Filleur, S ;
Gan, YB ;
Forde, BG .
PHOTOSYNTHESIS RESEARCH, 2005, 83 (02) :239-250
[58]   Genomic analysis of a nutrient response in arabidopsis reveals diverse expression patterns and novel metabolic and potential regulatory genes induced by nitrate [J].
Wang, RC ;
Guegler, K ;
LaBrie, ST ;
Crawford, NM .
PLANT CELL, 2000, 12 (08) :1491-1509
[59]   Genomic analysis of the nitrate response using a nitrate reductase-null mutant of Arabidopsis [J].
Wang, RC ;
Tischner, R ;
Gutiérrez, RA ;
Hoffman, M ;
Xing, XJ ;
Chen, MS ;
Coruzzi, G ;
Crawford, NM .
PLANT PHYSIOLOGY, 2004, 136 (01) :2512-2522
[60]   Microarray analysis of the nitrate response in Arabidopsis roots and shoots reveals over 1,000 rapidly responding genes and new linkages to glucose, trehalose-6-phosphate, iron, and sulfate metabolism [J].
Wang, RC ;
Okamoto, M ;
Xing, XJ ;
Crawford, NM .
PLANT PHYSIOLOGY, 2003, 132 (02) :556-567