Kuusk Silja, Sørlie Morten, Väljamäe Priit
Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Department of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, Ås, Norway.
PLoS One. 2017 Jan 27;12(1):e0171042. doi: 10.1371/journal.pone.0171042. eCollection 2017.
Human chitotriosidase (HCHT) is involved in immune response to chitin-containing pathogens in humans. The enzyme is able to degrade chitooligosaccharides as well as crystalline chitin. The catalytic domain of HCHT is connected to the carbohydrate binding module (CBM) through a flexible hinge region. In humans, two active isoforms of HCHT are found-the full length enzyme and its truncated version lacking CBM and the hinge region. The active site architecture of HCHT is reminiscent to that of the reducing-end exo-acting processive chitinase ChiA from bacterium Serratia marcescens (SmChiA). However, the presence of flexible hinge region and occurrence of two active isoforms are reminiscent to that of non-processive endo-chitinase from S. marcescens, SmChiC. Although the studies on soluble chitin derivatives suggest the endo-character of HCHT, the mode of action of the enzyme on crystalline chitin is not known. Here, we made a thorough characterization of HCHT in terms of the mode of action, processivity, binding, and rate constants for the catalysis and dissociation using α-chitin as substrate. HCHT efficiently released the end-label from reducing-end labelled chitin and had also high probability (95%) of endo-mode initiation of processive run. These results qualify HCHT as an endo-processive enzyme. Processivity and the rate constant of dissociation of HCHT were found to be in-between those, characteristic to processive exo-enzymes, like SmChiA and randomly acting non-processive endo-enzymes, like SmChiC. Apart from increasing the affinity for chitin, CBM had no major effect on kinetic properties of HCHT.
人几丁质酶(HCHT)参与人体对含几丁质病原体的免疫反应。该酶能够降解低聚几丁质以及结晶几丁质。HCHT的催化结构域通过一个柔性铰链区与碳水化合物结合模块(CBM)相连。在人类中,发现了HCHT的两种活性同工型——全长酶及其缺少CBM和铰链区的截短版本。HCHT的活性位点结构让人联想到来自粘质沙雷氏菌(SmChiA)的还原性末端外切作用连续性几丁质酶ChiA。然而,柔性铰链区的存在以及两种活性同工型的出现让人联想到来自粘质沙雷氏菌的非连续性内切几丁质酶SmChiC。尽管对可溶性几丁质衍生物的研究表明HCHT具有内切特性,但该酶对结晶几丁质的作用模式尚不清楚。在此,我们以α-几丁质为底物,对HCHT在作用模式、连续性、结合以及催化和解离速率常数方面进行了全面表征。HCHT能有效地从还原性末端标记的几丁质上释放末端标记,并且具有很高的概率(95%)以内切模式启动连续性反应。这些结果表明HCHT是一种内切连续性酶。HCHT的连续性和解离速率常数介于连续性外切酶(如SmChiA)和随机作用的非连续性内切酶(如SmChiC)的特征值之间。除了增加对几丁质的亲和力外,CBM对HCHT的动力学性质没有重大影响。