首页> 外文期刊>Journal of general plant pathology >D-alanine-D-alanine ligase gene (ddl) of Erwinia chrysanthemi strain EC16 II: analysis of pectate lyase regulation using ddl~- mutant
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D-alanine-D-alanine ligase gene (ddl) of Erwinia chrysanthemi strain EC16 II: analysis of pectate lyase regulation using ddl~- mutant

机译:菊花欧文氏菌EC16 II的D-丙氨酸-D-丙氨酸连接酶基因(ddl):使用ddl〜-突变体对果胶酸裂解酶调控的分析

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摘要

Erwinia chrysanthemi (Ech) triggers soft rot disease mainly by secreting pectate lyase (Pel), which is regulated in a complex manner by many regulatory genes. In a previous study, we used a gene dosage method to show that the ddl gene, which encodesD-alanine-D-alanine ligase, reduced Pel production and tissue maceration by Ech strain EC16n. In this study, the ddl~- marker-exchanged mutant was shown to overcome the long growth lag caused by various salts in the growth medium and to increase Pel production over that by EC16n, especially in a medium containing magnesium salts. Thus, ddl seems to regulate Pel production in a negative manner. Because the profiles of a gel shift assay using the pelE promoter region as the target DNA with crude extractsof EC16n and ddl~- mutant were distinguishable, Ddl is thought to affect the binding of other regulatory proteins. Expression of the ddl gene was induced in the medium containing a low-molecular-weight fraction of potato extract, but it was reduced in that containing both polygalacturonic acid (PGA) and the fraction. The repression of ddl expression by PGA should contribute in part to the in planta hyperinduction of Pel.
机译:菊花欧文氏菌(Ech)主要通过分泌果胶酸裂合酶(Pel)触发软腐病,果胶裂合酶由许多调控基因以复杂的方式调控。在以前的研究中,我们使用一种基因剂量方法来显示编码D-丙氨酸-D-丙氨酸连接酶的ddl基因减少了Ech菌株EC16n的Pel产生和组织浸软。在这项研究中,ddl〜-标记交换的突变体显示克服了生长培养基中各种盐引起的长生长滞后,并且比EC16n尤其是在含有镁盐的培养基中提高了Pel产量。因此,ddl似乎以负面的方式调节了Pel的生产。因为使用pelE启动子区域作为目标DNA以及EC16n和ddl_-突变体的粗提物进行凝胶迁移分析的谱图是可区分的,所以Ddl被认为会影响其他调控蛋白的结合。在含有低分子量马铃薯提取物组分的培养基中诱导了ddl基因的表达,但在同时含有聚半乳糖醛酸(PGA)和该组分的培养基中其表达降低了。 PGA对ddl表达的抑制作用应部分有助于植物体内Pel的过度诱导。

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