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玉米中编码几丁质分解酶的基因的全基因组鉴定、表达及染色体定位

Genome-wide identification, expression and chromosomal location of the genes encoding chitinolytic enzymes in Zea mays.

作者信息

Shoresh Michal, Harman Gary E

机构信息

Department of Horticultural Sciences, Cornell University, Geneva, NY 14456, USA.

出版信息

Mol Genet Genomics. 2008 Aug;280(2):173-85. doi: 10.1007/s00438-008-0354-1. Epub 2008 Jun 17.

Abstract

Chitinolytic enzymes are important pathogenesis and stress related proteins. We identified 27 putative genes encoding endochitinases in the maize genome via in silico techniques and four exochitinases. Only seven of the endochitinases and segments of the exochitinases were heretofore known. The endochitinases included members of family 19 chitinases (classes I-IV of PR3, II of PR4) and members of family 18 chitinases (class III of PR8). Some similar enzymes were detected on adjacent regions of the same chromosome, and seem to result from duplication events. Most of the genes expressed were identified from EST libraries from plants exposed to biotic or abiotic stresses but also from libraries from tissues not exposed to stresses. We isolated proteins from seedlings of maize in the presence or absence of the symbiotic root colonizing fungus Trichoderma harzianum strain T22, and analyzed the activity of chitinolytic enzymes using an in-gel activity assay. The activity bands were identified by LC/MS/MS using the database from our in silico study. The identities of the enzymes changed depending on whether or not T22 was present. One activity band of about 95 kDa appeared to be a heterodimer between an exochitinase and any of several different endochitinases. The identity of the endochitinase component appeared to be dependent upon treatment.

摘要

几丁质分解酶是与致病机制和胁迫相关的重要蛋白质。我们通过电子克隆技术在玉米基因组中鉴定出27个推定的编码内切几丁质酶的基因和4个外切几丁质酶基因。此前仅知晓其中7个内切几丁质酶和外切几丁质酶的片段。内切几丁质酶包括19家族几丁质酶成员(PR3的I-IV类、PR4的II类)和18家族几丁质酶成员(PR8的III类)。在同一条染色体的相邻区域检测到了一些相似的酶,它们似乎是由基因复制事件产生的。大多数表达的基因是从暴露于生物或非生物胁迫的植物的EST文库中鉴定出来的,但也有一些来自未暴露于胁迫的组织的文库。我们在有或没有共生根定殖真菌哈茨木霉T22菌株存在的情况下,从玉米幼苗中分离蛋白质,并使用凝胶内活性测定法分析几丁质分解酶的活性。利用我们电子克隆研究的数据库,通过LC/MS/MS鉴定活性条带。酶的身份根据T22是否存在而变化。一条约95 kDa的活性条带似乎是一种外切几丁质酶与几种不同内切几丁质酶中的任何一种之间形成的异二聚体。内切几丁质酶成分的身份似乎取决于处理方式。

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