A functional genomics investigation of allelochemical biosynthesis in Sorghum bicolor root hairs

被引:72
作者
Baerson, Scott R. [1 ]
Dayan, Franck E. [1 ]
Rimando, Agnes M. [1 ]
Nanayakkara, N. P. Dhammika [2 ]
Liu, Chang-Jun [3 ]
Schroerder, Joachim [4 ]
Fishbein, Mark [5 ]
Pan, Zhiqiang [1 ]
Kagan, Isabelle A. [1 ]
Pratt, Lee H. [6 ]
Le Cordonnier-Pratt, Marie-Miche [6 ]
Duke, Stephen O. [1 ]
机构
[1] USDA ARS, Nat Prod Utilizat Res Unit, University, MS 38677 USA
[2] Univ Mississippi, Sch Pharm, Natl Ctr Nat Prod Res, University, MS 38677 USA
[3] Brookhaven Natl Lab, Dept Biol, Upton, NY 11973 USA
[4] Univ Freiburg, Inst Biol 2, D-79104 Freiburg, Germany
[5] Portland State Univ, Dept Biol, Portland, OR 97207 USA
[6] Univ Georgia, Dept Plant Biol, Athens, GA 30602 USA
关键词
D O I
10.1074/jbc.M706587200
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
Sorghum is considered to be one of the more allelopathic crop species, producing phytotoxins such as the potent benzoquinone sorgoleone (2-hydroxy-5-methoxy-3-[(Z,Z)-8',11',14'-pentadecatriene]-p-benzoquinone) and its analogs. Sorgoleone likely accounts for much of the allelopathy of Sorghum spp., typically representing the predominant constituent of Sorghum bicolor root exudates. Previous and ongoing studies suggest that the biosynthetic pathway for this plant growth inhibitor occurs in root hair cells, involving a polyketide synthase activity that utilizes an atypical 16:3 fatty acyl-CoA starter unit, resulting in the formation of a pentadecatrienyl resorcinol intermediate. Subsequent modifications of this resorcinolic intermediate are likely to be mediated by S-adenosylmethionine-dependent O-methyltransferases and dihydroxylation by cytochrome P450 monooxygenases, although the precise sequence of reactions has not been determined previously. Analyses performed by gas chromatography-mass spectrometry with sorghum root extracts identified a 3-methyl ether derivative of the likely pentadecatrienyl resorcinol intermediate, indicating that dihydroxylation of the resorcinol ring is preceded by O-methylation at the 3'-position by a novel 5-n-alk(en)ylresorcinol-utilizing O-methyltransferase activity. An expressed sequence tag data set consisting of 5,468 sequences selected at random from an S. bicolor root hair-specific cDNA library was generated to identify candidate sequences potentially encoding enzymes involved in the sorgoleone biosynthetic pathway. Quantitative real time reverse transcription-PCR and recombinant enzyme studies with putative O-methyltransferase sequences obtained from the expressed sequence tag data set have led to the identification of a novel O-methyltransferase highly and predominantly expressed in root hairs (designated SbOMT3), which preferentially utilizes alk(en)ylresorcinols among a panel of benzene-derivative substrates tested. SbOMT3 is therefore proposed to be involved in the biosynthesis of the allelochemical sorgoleone.
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收藏
页码:3231 / 3247
页数:17
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