Wallaart T E, Bouwmeester H J, Hille J, Poppinga L, Maijers N C
GenoClipp Biotechnology BV, Meditech Center, Groningen, The Netherlands.
Planta. 2001 Feb;212(3):460-5. doi: 10.1007/s004250000428.
The sesquiterpenoid artemisinin, isolated these from the plant Artemisia annua L., and its semi-synthetic derivatives are a new and very effective group of antimalarial drugs. A branch point in the biosynthesis of this compound is the cyclisation of the ubiquitous precursor farnesyl diphosphate into the first specific precursor of artemisinin, namely amorpha-4,11-diene. Here we describe the isolation of a cDNA clone encoding amorpha-4,11-diene synthase. The deduced amino acid sequence exhibits the highest identity (50%) with a putative sesquiterpene cyclase of A. annua. When expressed in Escherichia coli, the recombinant enzyme catalyses the formation of amorpha-4,11-diene from farnesyl diphosphate. Introduction of the gene into tobacco (Nicotiana tabacum L.) resulted in the expression of an active enzyme and the accumulation of amorpha-4,11-diene ranging from 0.2 to 1.7 ng per g fresh weight.
从植物黄花蒿中分离得到的倍半萜青蒿素及其半合成衍生物是一类新型且非常有效的抗疟药物。该化合物生物合成的一个分支点是普遍存在的前体法呢基二磷酸环化形成青蒿素的第一个特定前体,即紫穗槐 -4,11- 二烯。在此,我们描述了一个编码紫穗槐 -4,11- 二烯合酶的 cDNA 克隆的分离。推导的氨基酸序列与黄花蒿假定的倍半萜环化酶具有最高的同一性(50%)。当在大肠杆菌中表达时,重组酶催化法呢基二磷酸形成紫穗槐 -4,11- 二烯。将该基因导入烟草(烟草)导致活性酶的表达以及紫穗槐 -4,11- 二烯的积累,积累量为每克鲜重 0.2 至 1.7 纳克。