Valine Pathway Is More Crucial than Phenyl Propanoid Pathway in Regulating Capsaicin Biosynthesis in Capsicum frutescens Mill.
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文摘
Capsaicin, a pungency factor alkaloid of Capsicum fruits, is biosynthesized by enzymatic condensationof vanillylamine, a phenyl propanoid intermediate, and 8-methyl-nonenoic acid, a fatty acid derivativefrom the leucine/valine pathway by capsaicin synthase. Biotic elicitors, such as aqueous mycelialextracts of Rhizopus oligosporus and Aspergillus niger, and abiotic elicitors, such as salicylic acidand methyl jasmonate, were incorporated to cell-suspension cultures of Capsicum frutescens. Themaximum elicitation of capsaicinoids to the extent of 6-folds was noticed when mycelial extracts ofR. oligosporus were incorporated to cell-suspension cultures. The phenyl propanoid intermediateswere elicited to the extent of 3-4-fold, whereas the levels of 8-methyl-nonanoic acid increased 6-foldin R. oligosporus mycelial-extract-treated cultures. The enzymatic assays of caffeic acid O-methyltransferases, keto acyl synthase, and capsaicin synthase were performed in elicited and nonelicitedcell-suspension cultures. These enzymes were overexpressed in R. oligosporus mycelial-extract-treated suspension cultures, which was also confirmed by reverse transcriptase polymerase chainreaction studies. This is the first paper on the overexpression of 8-methyl-nonanoic acid leading tocapsaicin biosynthesis using elicitors.

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