Tóth Ákos, Barna Terézia, Szabó Erna, Elek Rita, Hubert Ágnes, Nagy István, Nagy István, Kriszt Balázs, Táncsics András, Kukolya József
Department of Applied and Environmental Microbiology, National Agricultural Research and Innovation Centre, Budapest, Hungary.
Department of Genetics and Applied Microbiology, University of Debrecen, Hungary.
PLoS One. 2016 May 25;11(5):e0155769. doi: 10.1371/journal.pone.0155769. eCollection 2016.
Thermobifidas are thermotolerant, compost inhabiting actinomycetes which have complex polysaccharide hydrolyzing enzyme systems. The best characterized enzymes of these hydrolases are cellulases from T. fusca, while other important enzymes especially hemicellulases are not deeply explored. To fill this gap we cloned and investigated endomannanases from those reference strains of the Thermobifida genus, which have published data on other hydrolases (T. fusca TM51, T. alba CECT3323, T. cellulosilytica TB100T and T. halotolerans YIM90462T). Our phylogenetic analyses of 16S rDNA and endomannanase sequences revealed that T. alba CECT3323 is miss-classified; it belongs to the T. fusca species. The cloned and investigated endomannanases belong to the family of glycosyl hydrolases 5 (GH5), their size is around 50 kDa and they are modular enzymes. Their catalytic domains are extended by a C-terminal carbohydrate binding module (CBM) of type 2 with a 23-25 residues long interdomain linker region consisting of Pro, Thr and Glu/Asp rich repetitive tetrapeptide motifs. Their polypeptide chains exhibit high homology, interdomain sequence, which don't show homology to each other, but all of them are built up from 3-6 times repeated tetrapeptide motifs) (PTDP-Tc, TEEP-Tf, DPGT-Th). All of the heterologously expressed Man5A enzymes exhibited activity only on mannan. The pH optima of Man5A enzymes from T. halotolerans, T. cellulosilytica and T. fusca are slightly different (7.0, 7.5 and 8.0, respectively) while their temperature optima span within the range of 70-75°C. The three endomannanases exhibited very similar kinetic performances on LBG-mannan substrate: 0.9-1.7mM of KM and 80-120 1/sec of turnover number. We detected great variability in heat stability at 70°C, which was influenced by the presence of Ca2+. The investigated endomannanases might be important subjects for studying the structure/function relation behind the heat stability and for industrial applications to hemicellulose degradation.
嗜热栖热放线菌是一类耐热、栖息于堆肥中的放线菌,具有复杂的多糖水解酶系统。这些水解酶中最具特征的酶是来自黄褐栖热放线菌的纤维素酶,而其他重要的酶,尤其是半纤维素酶,尚未得到深入研究。为了填补这一空白,我们从嗜热栖热放线菌属的那些参考菌株中克隆并研究了内切甘露聚糖酶,这些菌株已发表了关于其他水解酶的数据(黄褐栖热放线菌TM51、白色栖热放线菌CECT3323、解纤维素栖热放线菌TB100T和耐盐栖热放线菌YIM90462T)。我们对16S rDNA和内切甘露聚糖酶序列的系统发育分析表明,白色栖热放线菌CECT3323分类错误;它属于黄褐栖热放线菌种。克隆并研究的内切甘露聚糖酶属于糖基水解酶5(GH5)家族,其大小约为50 kDa,是模块化酶。它们的催化结构域由2型C末端碳水化合物结合模块(CBM)延伸,具有一个由富含Pro、Thr和Glu/Asp的重复四肽基序组成的23 - 25个残基长的结构域间连接区。它们的多肽链表现出高度同源性,结构域间序列彼此不显示同源性,但它们都是由3 - 6次重复的四肽基序构建而成(PTDP - Tc、TEEP - Tf、DPGT - Th)。所有异源表达的Man5A酶仅对甘露聚糖表现出活性。耐盐栖热放线菌、解纤维素栖热放线菌和黄褐栖热放线菌的Man5A酶的最适pH值略有不同(分别为7.0、7.5和8.0),而它们的最适温度范围在70 - 75°C之间。这三种内切甘露聚糖酶对LBG - 甘露聚糖底物表现出非常相似的动力学性能:KM为0.9 - 1.7 mM,周转数为80 - 120 1/秒。我们检测到在70°C下热稳定性存在很大差异,这受到Ca2 +存在的影响。所研究的内切甘露聚糖酶可能是研究热稳定性背后的结构/功能关系以及用于半纤维素降解工业应用的重要对象。