Hamilton A J, Bouzayen M, Grierson D
Department of Physiology and Environmental Science, University of Nottingham School of Agriculture, Sutton Bonington, Loughborough, United Kingdom.
Proc Natl Acad Sci U S A. 1991 Aug 15;88(16):7434-7. doi: 10.1073/pnas.88.16.7434.
The ethylene-forming enzyme (EFE), which catalyzes the last step in the biosynthesis of the plant hormone ethylene, has never been purified and no molecular probes are available. Recently, a putative cDNA clone for tomato EFE (pTOM13) has been identified by inhibiting ethylene synthesis with an antisense gene expressed in transgenic plants. A direct test of its function has been made by expression of a pTOM13 gene in Saccharomyces cerevisiae. After cloning artefacts were discovered in the 5' region of the cDNA, a corrected cDNA (pRC13) was created by the fusion of the 5' end of a genomic clone to the 3' end of the cDNA and expressed in S. cerevisiae. Cultures of transformed yeast converted 1-aminocyclopropane-1-carboxylic acid (ACC) to ethylene, whereas control cells did not. This EFE activity displays similar characteristics to EFE found in plant tissue: it converts the trans isomer of the ACC analogue 1-amino-2-ethylcyclopropane-1-carboxylic acid to 1-butene in preference to the cis isomer, and it is strongly inhibited by cobaltous ions and 1,10-phenanthroline. Furthermore, information gained from the activity of effectors on yeast EFE activity supports the hypothesis that EFE is one of a group of hydroxylase enzymes.
乙烯形成酶(EFE)催化植物激素乙烯生物合成的最后一步,该酶从未被纯化,也没有可用的分子探针。最近,通过在转基因植物中表达反义基因抑制乙烯合成,已鉴定出番茄EFE的一个推定cDNA克隆(pTOM13)。通过在酿酒酵母中表达pTOM13基因对其功能进行了直接测试。在cDNA的5'区域发现克隆假象后,通过将基因组克隆的5'末端与cDNA的3'末端融合创建了一个校正的cDNA(pRC13),并在酿酒酵母中表达。转化酵母培养物将1-氨基环丙烷-1-羧酸(ACC)转化为乙烯,而对照细胞则不能转化。这种EFE活性表现出与植物组织中发现的EFE相似的特征:它优先将ACC类似物1-氨基-2-乙基环丙烷-1-羧酸的反式异构体转化为1-丁烯,而不是顺式异构体,并且它受到钴离子和1,10-菲咯啉的强烈抑制。此外,从效应物对酵母EFE活性的影响中获得的信息支持了EFE是一组羟化酶之一的假设。