Steenbakkers P J, Li X L, Ximenes E A, Arts J G, Chen H, Ljungdahl L G, Op Den Camp H J
Department of Microbiology, Faculty of Science, University of Nijmegen, NL-6525 ED Nijmegen, The Netherlands.
J Bacteriol. 2001 Sep;183(18):5325-33. doi: 10.1128/JB.183.18.5325-5333.2001.
A method is presented for the specific isolation of genes encoding cellulosome components from anaerobic fungi. The catalytic components of the cellulosome of anaerobic fungi typically contain, besides the catalytic domain, mostly two copies of a 40-amino-acid cysteine-rich, noncatalytic docking domain (NCDD) interspaced by short linkers. Degenerate primers were designed to anneal to the highly conserved region within the NCDDs of the monocentric fungus Piromyces sp. strain E2 and the polycentric fungus Orpinomyces sp. strain PC-2. Through PCR using cDNA from Orpinomyces sp. and genomic DNA from Piromyces sp. as templates, respectively, 9 and 19 PCR products were isolated encoding novel NCDD linker sequences. Screening of an Orpinomyces sp. cDNA library with four of these PCR products resulted in the isolation of new genes encoding cellulosome components. An alignment of the partial NCDD sequence information obtained and an alignment of database-accessible NCDD sequences, focusing on the number and position of cysteine residues, indicated the presence of three structural subfamilies within fungal NCDDs. Furthermore, evidence is presented that the NCDDs in CelC from the polycentric fungus Orpinomyces sp. strain PC-2 specifically recognize four proteins in a cellulosome preparation, indicating the presence of multiple scaffoldins.
本文介绍了一种从厌氧真菌中特异性分离编码纤维小体组分基因的方法。厌氧真菌纤维小体的催化组分除催化结构域外,通常还含有两个拷贝的富含半胱氨酸的40个氨基酸的非催化对接结构域(NCDD),由短连接子间隔。设计简并引物,使其与单中心真菌皮罗霉菌株E2和多中心真菌奥尔平霉菌株PC-2的NCDD内的高度保守区域退火。分别以奥尔平霉菌的cDNA和皮罗霉菌的基因组DNA为模板进行PCR,分离得到9个和19个编码新型NCDD连接子序列的PCR产物。用其中4个PCR产物筛选奥尔平霉菌的cDNA文库,得到了编码纤维小体组分的新基因。对获得的部分NCDD序列信息与数据库中可获取的NCDD序列进行比对,重点关注半胱氨酸残基的数量和位置,结果表明真菌NCDD中存在三个结构亚家族。此外,有证据表明,多中心真菌奥尔平霉菌株PC-2的CelC中的NCDD能特异性识别纤维小体制剂中的四种蛋白质,这表明存在多种支架蛋白。