Montero M, Sanz L, Rey M, Llobell A, Monte E
Centro Hispano-Luso de Investigaciones Agrarias, Universidad de Salamanca, Salamanca, Spain.
J Appl Microbiol. 2007 Oct;103(4):1291-300. doi: 10.1111/j.1365-2672.2007.03371.x.
To clone and characterize the gene coding for BGN16.3, a beta-1,6-glucanase putatively implicated in mycoparasitism by Trichoderma harzianum, a biocontrol agent used against plant pathogenic fungi.
Using degenerate primed PCR and cDNA library screening, we have cloned the cDNA coding BGN16.3. bgn16.3 showed a significant sequence identity (50%) to bgn16.1; however, they both have low identity to the previously cloned bgn16.2, allowing the identification of amino acid sequences putatively involved in the common catalytic activity of the three proteins. bgn16.3 is a single-copy gene and highly homologous sequences are present in all tested Trichoderma species. bgn16.3 expression pattern is analysed by Northern blot, finding that it is expressed during the interaction of T. harzianum CECT 2413 with Botrytis cinerea, supporting the implication of the enzyme in the mycoparasitic process.
The cloned bgn16.3 completes the knowledge on the beta-1,6-glucanase isozyme system from T. harzianum CECT 2413. A highly homologous gene is present in all analysed Trichoderma strains. bgn16.3 is expressed under few specific conditions, including the mycoparasitic process.
This study contributes to the knowledge of beta-1,6-glucanases. It implicates this group of enzymes in the mycoparasitism by some biocontrol agents such as T. harzianum.
克隆并鉴定编码BGN16.3的基因,BGN16.3是一种β-1,6-葡聚糖酶,推测参与哈茨木霉的真菌寄生作用,哈茨木霉是一种用于防治植物病原真菌的生防菌。
利用简并引物PCR和cDNA文库筛选,我们克隆了编码BGN16.3的cDNA。bgn16.3与bgn16.1具有显著的序列同一性(50%);然而,它们与先前克隆的bgn16.2的同一性都很低,这使得我们能够鉴定出可能参与这三种蛋白质共同催化活性的氨基酸序列。bgn16.3是一个单拷贝基因,在所有测试的木霉菌种中都存在高度同源的序列。通过Northern印迹分析bgn16.3的表达模式,发现它在哈茨木霉CECT 2413与灰葡萄孢相互作用期间表达,这支持了该酶在真菌寄生过程中的作用。
克隆的bgn16.3完善了对哈茨木霉CECT 2413的β-1,6-葡聚糖酶同工酶系统的认识。在所有分析的木霉菌株中都存在一个高度同源的基因。bgn16.3在少数特定条件下表达,包括真菌寄生过程。
本研究有助于了解β-1,6-葡聚糖酶。它表明这类酶在一些生防菌如哈茨木霉的真菌寄生作用中发挥作用。