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Amorpha-4,11-diene synthase of Artemisia annua: cDNA isolation and bacterial expression of a terpene synthase involved in artemisinin biosynthesis

机译:青蒿的Amorpha-4,11-二烯合酶:青蒿素生物合成中涉及的萜烯合酶的cDNA分离和细菌表达

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摘要

Artemisia annua, an indigenous plant to Korea, contains an antimalarial sesquiterpene, artemisinin. The first committed step of artemisinin biosynthesis is the cyclization of farnesyl diphosphate by a sesquiterpene synthase to produce an amorphane-type ring system. The aims of this research were to molecularly clone and express amorpha-4,11-diene synthase for metabolic engineering. PCR amplification of genomic DNA with a pair of primers, designed from the conserved regions of sesquiterpene synthases of several plants, produced a 184-bp DNA fragment. This fragment was used in Northern blot analysis as a probe, showing approximately 2.2 kb of a single band. Its sequence information was used to produce 2106 bp of a full-length cDNA sequence including 1641 bp of open reading frame for 546 amino acids (kcs12) through a rapid amplification of cDNA ends (RACE). The deduced amino acid sequence displayed 36% identity with 5-epi-aristolochene synthase of Nicotiana tabacum. A soluble fraction of Escherichia coli harboring kcs12 catalyzed the cyclization of farnesyl diphosphate to produce a sesquiterpene, which was identified through GC-MS analysis as amorpha-4,11-diene. (C) 2000 Academic Press. [References: 28]
机译:青蒿,韩国的一种本土植物,含有抗疟倍半萜,青蒿素。青蒿素生物合成的第一个重要步骤是倍半萜烯合酶对法呢基二磷酸的环化作用,以产生一个吗啡型环系统。这项研究的目的是分子克隆和表达用于代谢工程的amorpha-4,11-diene合酶。从一对植物的倍半萜合酶的保守区设计的一对引物对基因组DNA进行PCR扩增,产生了一个184 bp的DNA片段。该片段在RNA印迹分析中用作探针,显示约2.2kb的单条带。它的序列信息用于通过快速扩增cDNA末端(RACE)产生2106 bp的全长cDNA序列,其中包括546个氨基酸(kcs12)的1641 bp的开放阅读框。推导的氨基酸序列与烟草的5-表位-aristolochene合酶具有36%的同一性。带有kcs12的大肠杆菌可溶级分催化法呢基二磷酸的环化生成倍半萜,通过GC-MS分析鉴定该倍半萜为amorpha-4,11-diene。 (C)2000年学术出版社。 [参考:28]

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