Cloning and characterization of farnesyl pyphosphate synthase gene from the ABA-producing fungi Botrytis cinerea.

Hong-Yuan Deng, Xin-Rong Ma, Zhi-Dong Li, Hong Tan
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引用次数: 2

Abstract

Farnesyl pyphosphate synthase (FPPS) catalyzes the systhesis of farnesyl pyphosphate and appears to be a promising regulation site of Abscisic acid (ABA) biosynthesis pathway in fungi. Here we reported the isolation and characterization of Botrytis cinerea (FPPS) gene. The cloned FPPS gene carries an open reading frame of 1044-bp encoding a deduced protein of 347 amino acids with a molecular weight of 39.83 kDa, and the coding region is interrupted with a 63-bp intron. Comparison analysis showed that the deduced amino acids sequence share high similarity with other known FPPS gene. Southern blot revealed a single copy of FPPS gene in the genomic DNA. The result of transcription analysis indicated that the cloned FPPS gene expressed constitutively and was not induced in ABA accumulation phase.

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产aba真菌灰霉病菌法尼基磷酸合酶基因的克隆与鉴定。
法尼尼基磷酸合酶(FPPS)是一种催化法尼尼基磷酸合成的酶,是真菌脱落酸(ABA)生物合成途径中一个很有前景的调控位点。本文报道了灰葡萄孢(Botrytis cinerea, FPPS)基因的分离与鉴定。克隆的FPPS基因全长1044-bp,编码347个氨基酸,分子量为39.83 kDa,编码区被一个63-bp的内含子打断。比较分析表明,推导出的氨基酸序列与其他已知的FPPS基因具有较高的相似性。在基因组DNA中发现了一个FPPS基因拷贝。转录分析结果表明,克隆的FPPS基因在ABA积累期不受诱导,具有组构性表达。
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