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首页> 外文期刊>Molecular Microbiology >The txtAB genes of the plant pathogen Streptomyces acidiscabies encode a peptide synthetase required for phytotoxin thaxtomin A production and pathogenicity.
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The txtAB genes of the plant pathogen Streptomyces acidiscabies encode a peptide synthetase required for phytotoxin thaxtomin A production and pathogenicity.

机译:植物病原体酸性链霉菌的txtAB基因编码植物毒素thaxtomin A产生和致病性所需的肽合成酶。

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摘要

Four Streptomyces species have been described as the causal agents of scab disease, which affects economically important root and tuber crops worldwide. These species produce a family of cyclic dipeptides, the thaxtomins, which alone mimic disease symptomatology. Structural considerations suggest that thaxtomins are synthesized non-ribosomally. Degenerate oligonucleotide primers were used to amplify conserved portions of the acyladenylation module of peptide synthetase genes from genomic DNA of representatives of the four species. Pairwise Southern hybridizations identified a peptide synthetase acyladenylation module conserved among three species. The complete nucleotide sequences of two peptide synthetase genes (txtAB) were determined from S. acidiscabies 84.104 cosmid library clones. The organization of the deduced TxtA and TxtB peptide synthetase catalytic domains is consistent with the formation of N-methylated cyclic dipeptides such as thaxtomins. Based on high-performance liquid chromatography (HPLC) analysis, thaxtomin A production was abolished in txtA gene disruption mutants. Although the growth and morphological characteristics of the mutants were identical to those of the parent strain, txtA mutants were avirulent on potato tubers. Moreover, introduction of the thaxtomin synthetase cosmid into a txtA mutant restored both pathogenicity and thaxtomin A production, demonstrating a critical role for thaxtomins in pathogenesis.
机译:四种链霉菌已被描述为sc疮病的病原体,这种病会影响全球经济上重要的块根和块茎作物。这些物种产生了一个环状二肽家族,thaxtomins,仅模仿疾病的症状。结构上的考虑表明,Thaxtomin是非核糖体合成的。简并的寡核苷酸引物用于从四种物种代表的基因组DNA中扩增肽合成酶基因的酰基腺苷酸化模块的保守部分。成对的Southern杂交鉴定了在三个物种之间保守的肽合成酶酰化腺苷酸化模块。从酸性葡萄球菌84.104粘粒文库克隆中确定了两个肽合成酶基因(txtAB)的完整核苷酸序列。推导的TxtA和TxtB肽合成酶催化域的组织与N-甲基化的环二肽(如Thaxtomin)的形成是一致的。基于高效液相色谱(HPLC)分析,在txtA基因破坏突变体中取消了thaxtomin A的产生。尽管该突变体的生长和形态特征与亲本菌株相同,但txtA突变体在马铃薯块茎上无毒。此外,将凝血酶原合成酶粘粒引入txtA突变体可恢复致病性和凝血酶原A的产生,这证明了凝血酶原在发病机理中的关键作用。

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