Takenaka Shoko, Ohnuma Takayuki, Fukamizo Tamo
1 Department of Advanced Bioscience, Kindai University.
J Appl Glycosci (1999). 2017 May 20;64(2):39-42. doi: 10.5458/jag.jag.JAG-2016_015. eCollection 2017.
Chitinases belonging to the GH19 family have diverse loop structure arrangements. A GH19 chitinase from rye seeds (RSC-c) has a full set of (six) loop structures that form an extended binding cleft from -4 to +4 ("loopful"), while that from moss (BcChi-A) lacks several loops and forms a shortened binding cleft from -2 to +2 ("loopless"). We herein inserted a loop involved in sugar residue binding at subsites +3 and +4 of RSC-c (Loop-II) into BcChi-A (BcChi-A+L-II), and the thermal stability and enzymatic activity of BcChi-A+L-II were then characterized and compared with those of BcChi-A. The transition temperature of thermal unfolding decreased from 77.2 ˚C (BcChi-A) to 63.3 ˚C (BcChi-A+L-II) by insertion of Loop-II. Enzymatic activities toward the chitin tetramer (GlcNAc) and the polymeric substrate glycol chitin were also suppressed by the Loop-II insertion to 12 and 9 %, respectively. The Loop-II inserted into BcChi-A was found to be markedly flexible and disadvantageous for protein stability and enzymatic activity.
属于糖基水解酶19(GH19)家族的几丁质酶具有多样的环结构排列。来自黑麦种子的一种GH19几丁质酶(RSC-c)具有一整套(六个)环结构,这些环结构形成了一个从-4到+4的延伸结合裂隙(“满环”),而来自苔藓的几丁质酶(BcChi-A)则缺少几个环,形成了一个从-2到+2的缩短结合裂隙(“无环”)。我们在此将参与RSC-c在亚位点+3和+4处糖残基结合的一个环(环II)插入到BcChi-A中(BcChi-A+L-II),然后对BcChi-A+L-II的热稳定性和酶活性进行了表征,并与BcChi-A进行了比较。通过插入环II,热解折叠的转变温度从77.2℃(BcChi-A)降至63.3℃(BcChi-A+L-II)。环II的插入还分别将对几丁质四聚体(GlcNAc)和聚合物底物乙二醇几丁质的酶活性抑制到了12%和9%。发现插入到BcChi-A中的环II具有明显的柔性,对蛋白质稳定性和酶活性不利。