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通过表达S-腺苷甲硫氨酸水解酶的转基因番茄降低乙烯合成。

Reduced ethylene synthesis by transgenic tomatoes expressing S-adenosylmethionine hydrolase.

作者信息

Good X, Kellogg J A, Wagoner W, Langhoff D, Matsumura W, Bestwick R K

机构信息

Agritope, Inc., Beaverton, OR 97008-7108.

出版信息

Plant Mol Biol. 1994 Nov;26(3):781-90. doi: 10.1007/BF00028848.

Abstract

We have utilized a gene from bacteriophage T3 that encodes the enzyme S-adenosylmethionine hydrolase (SAMase) to generate transgenic tomato plants that produce fruit with a reduced capacity to synthesize ethylene. S-adenosylmethionine (SAM) is the metabolic precursor of 1-aminocyclopropane-1-carboxylic acid, the proximal precursor to ethylene. SAMase catalyzes the conversion of SAM to methylthioadenosine and homoserine. To restrict the presence of SAMase to ripening fruit, the promoter from the tomato E8 gene was used to regulate SAMase gene expression. Transgenic tomato plants containing the 1.1 kb E8 promoter bore fruit that expressed SAMase during the breaker and orange stage of fruit ripening and stopped expression after the fruit fully ripened. Plants containing the 2.3 kb E8 promoter expressed SAMase at higher levels during the post-breaker phases of fruit ripening and had a substantially reduced capacity to synthesize ethylene.

摘要

我们利用了噬菌体T3中编码S-腺苷甲硫氨酸水解酶(SAMase)的基因来培育转基因番茄植株,这些植株所结的果实合成乙烯的能力降低。S-腺苷甲硫氨酸(SAM)是1-氨基环丙烷-1-羧酸的代谢前体,而1-氨基环丙烷-1-羧酸是乙烯的直接前体。SAMase催化SAM转化为甲硫基腺苷和高丝氨酸。为了使SAMase仅在成熟果实中存在,使用了来自番茄E8基因的启动子来调控SAMase基因的表达。含有1.1 kb E8启动子的转基因番茄植株所结的果实在果实成熟的破色期和橙色期表达SAMase,在果实完全成熟后停止表达。含有2.3 kb E8启动子的植株在果实成熟的破色后期阶段高水平表达SAMase,其合成乙烯的能力大幅降低。

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