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具有不同特异性的多聚半乳糖醛酸酶抑制蛋白(PGIPs)在菜豆中表达。

Polygalacturonase-inhibiting proteins (PGIPs) with different specificities are expressed in Phaseolus vulgaris.

作者信息

Desiderio A, Aracri B, Leckie F, Mattei B, Salvi G, Tigelaar H, Van Roekel J S, Baulcombe D C, Melchers L S, De Lorenzo G, Cervone F

机构信息

Dipartimento di Biologia Vegetale, Università' di Roma La Sapienza, Italy.

出版信息

Mol Plant Microbe Interact. 1997 Sep;10(7):852-60. doi: 10.1094/MPMI.1997.10.7.852.

Abstract

The pgip-1 gene of Phaseolus vulgaris, encoding a polygalacturonase-inhibiting protein (PGIP), PGIP-1 (P. Toubart, A. Desiderio, G. Salvi, F. Cervone, L. Daroda, G. De Lorenzo, C. Bergmann, A. G. Darvill, and P. Albersheim, Plant J. 2:367-373, 1992), was expressed under control of the cauliflower mosaic virus 35S promoter in tomato plants via Agrobacterium tumefaciens-mediated transformation. Transgenic tomato plants with different expression levels of PGIP-1 were used in infection experiments with the pathogenic fungi Fusarium oxysporum f. sp. lycopersici, Botrytis cinerea, and Alternaria solani. No evident enhanced resistance, compared with the resistance of untransformed plants, was observed. The pgip-1 gene was also transiently expressed in Nicotiana benthamiana with potato virus X (PVX) as a vector. PGIP-1 purified from transgenic tomatoes and PGIP-1 in crude protein extracts of PVX-infected N. benthamiana plants were tested with several fungal polygalacturonases (PGs). PGIP-1 from both plant sources exhibited a specificity different from that of PGIP purified from P. vulgaris (bulk bean PGIP). Notably, PGIP-1 was unable to interact with a homogeneous PG from Fusarium moniliforme, as determined by surface plasmon resonance analysis, while the bulk bean PGIP interacted with and inhibited this enzyme. Moreover, PGIP-1 expressed in tomato and N. benthamiana had only a limited capacity to inhibit crude PG preparations from F. oxysporum f. sp. lycopersici, B. cinerea, and A. solani. Differential affinity chromatography was used to separate PGIP proteins present in P. vulgaris extracts. A PGIP-A with specificity similar to that of PGIP-1 was separated from a PGIP-B able to interact with both Aspergillus niger and F. moniliforme PGs. Our data show that PGIPs with different specificities are expressed in P. vulgaris and that the high-level expression of one member (pgip-1) of the PGIP gene family in transgenic plants is not sufficient to confer general, enhanced resistance to fungi.

摘要

菜豆的pgip - 1基因编码一种多聚半乳糖醛酸酶抑制蛋白(PGIP),即PGIP - 1(P. 图巴特、A. 德西德里奥、G. 萨尔维、F. 塞尔沃内、L. 达罗达、G. 德洛伦佐、C. 伯格曼、A.G. 达维尔和P. 阿尔伯施海姆,《植物杂志》2:367 - 373,1992年),通过根癌农杆菌介导的转化在番茄植株中由花椰菜花叶病毒35S启动子控制表达。利用具有不同PGIP - 1表达水平的转基因番茄植株,对致病真菌尖孢镰刀菌番茄专化型、灰葡萄孢和链格孢进行感染实验。与未转化植株的抗性相比,未观察到明显增强的抗性。pgip - 1基因还利用马铃薯X病毒(PVX)作为载体在本氏烟草中瞬时表达。用几种真菌多聚半乳糖醛酸酶(PGs)对从转基因番茄中纯化的PGIP - 1和PVX感染的本氏烟草植株粗蛋白提取物中的PGIP - 1进行了测试。来自这两种植物来源的PGIP - 1表现出与从菜豆中纯化的PGIP(菜豆大宗PGIP)不同的特异性。值得注意的是,通过表面等离子体共振分析确定,PGIP - 1无法与来自串珠镰刀菌的一种纯合PG相互作用,而菜豆大宗PGIP能与该酶相互作用并抑制它。此外,在番茄和本氏烟草中表达的PGIP - 1对来自尖孢镰刀菌番茄专化型、灰葡萄孢和链格孢的粗PG制剂的抑制能力有限。采用差异亲和层析法分离菜豆提取物中存在的PGIP蛋白。从能够与黑曲霉和串珠镰刀菌的PGs相互作用的PGIP - B中分离出了一种特异性与PGIP - 1相似的PGIP - A。我们的数据表明,菜豆中表达了具有不同特异性的PGIPs,并且PGIP基因家族的一个成员(pgip - 1)在转基因植物中的高水平表达不足以赋予对真菌的普遍增强抗性。

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