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来自胶孢炭疽菌的果胶裂解酶在巨大炭疽菌中的表达促进致病性。

Expression of pectate lyase from Colletotrichum gloesosporioides in C. magna promotes pathogenicity.

作者信息

Yakoby N, Freeman S, Dinoor A, Keen N T, Prusky D

机构信息

Department of Postharvest Science of Fresh Produce, Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel.

出版信息

Mol Plant Microbe Interact. 2000 Aug;13(8):887-91. doi: 10.1094/MPMI.2000.13.8.887.

Abstract

To test the contribution of pectate lyase (PL) to promoting fungal pathogenicity, a pectate lyase gene (pel) from the avocado pathogen Colletotrichum gloeosporioides, isolate Cg-14, was expressed in C. magna isolate L-2.5, a pathogen of cucurbits that causes minor symptoms in watermelon seedlings and avocado fruits. Isolate L-2.5 was transformed with pPCPH-1 containing hph-B as a selectable marker and the 4.1-kb genomic pel clone. Southern hybridization, with the 4.1-kb genomic pel clone or 2.13-kb hph-B cassette as probes, detected integration of pel in transformed C. magna isolates Cm-PL-3 and Cm-PL-10. Western blot (immunoblot) analysis with antibodies against Cg-14 PL detected a single PL secreted by L-2.5 at a molecular mass of 41.5 kDa, whereas the PL of C. gloeosporioides had a molecular mass of 39 kDa. When PL activity was measured 4 days after inoculation in pectolytic enzyme-inducing media (PEIM), transformed isolates Cm-PL-3 and Cm-PL-10 showed additive PL activity relative to both Cg-14 and L-2.5. Transformed isolates also showed additive maceration capabilities on avocado pericarp relative to the wild-type C. magna alone, but did not reach the maceration ability of C. gloeosporioides. However, more severe maceration and damping off developed in watermelon seedlings inoculated with the transformed isolates compared with the two wild-type isolates, which showed no symptom development on these seedlings during the same period. Results clearly show the contribution of a single pel to the pathogenic abilities of C. magna and suggest that PL is a pathogenicity factor required for the penetration and colonization of Colletotrichum species.

摘要

为了测试果胶酸裂解酶(PL)对促进真菌致病性的作用,将来自鳄梨病原菌胶孢炭疽菌(Colletotrichum gloeosporioides)分离株Cg - 14的果胶酸裂解酶基因(pel)在大孢炭疽菌(C. magna)分离株L - 2.5中表达,L - 2.5是一种葫芦科病原菌,在西瓜幼苗和鳄梨果实上引起轻微症状。用含有潮霉素B(hph - B)作为选择标记和4.1 kb基因组pel克隆的pPCPH - 1对分离株L - 2.5进行转化。以4.1 kb基因组pel克隆或2.13 kb hph - B盒作为探针进行Southern杂交,检测到pel在转化的大孢炭疽菌分离株Cm - PL - 3和Cm - PL - 10中的整合。用针对Cg - 14 PL的抗体进行Western印迹(免疫印迹)分析,检测到L - 2.5分泌的一种单一PL,分子量为41.5 kDa,而胶孢炭疽菌的PL分子量为39 kDa。在接种于果胶分解酶诱导培养基(PEIM)4天后测量PL活性时,转化分离株Cm - PL - 3和Cm - PL - 10相对于Cg - 14和L - 2.5均表现出累加的PL活性。相对于单独的野生型大孢炭疽菌,转化分离株在鳄梨果皮上也表现出累加的浸解能力,但未达到胶孢炭疽菌的浸解能力。然而,与两种野生型分离株相比,接种转化分离株的西瓜幼苗出现了更严重的浸解和猝倒现象,而在同一时期野生型分离株在这些幼苗上未出现症状。结果清楚地表明单个pel对大孢炭疽菌致病能力的作用,并表明PL是炭疽菌属物种穿透和定殖所需的致病因子。

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