化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2014年
5期
1828-1834
,共7页
赵道辉%彭春望%廖晨伊%周健
趙道輝%彭春望%廖晨伊%週健
조도휘%팽춘망%료신이%주건
分子模拟%酶固定化%吸附取向%生物能源%蛋白质吸附
分子模擬%酶固定化%吸附取嚮%生物能源%蛋白質吸附
분자모의%매고정화%흡부취향%생물능원%단백질흡부
molecular simulation%enzyme immobilization%adsorption orientation%bioenergy%protein adsorption
利用酶固定化技术来对生物质发酵获取生物能源已显得日益重要。酶与表面间的相互作用强烈影响固定化酶的取向,进而影响催化效率。本文采用并行退火蒙特卡洛(PTMC)方法对三种生物能源用酶(脂肪酶、纤维素酶和氢化酶)在不同的带电表面和离子强度下的吸附取向进行了模拟研究。模拟结果发现三种酶的吸附主要由静电吸引力主导,并且很大程度上与蛋白表面带电氨基酸的分布和溶液离子的静电屏蔽有关。脂肪酶和氢化酶在带负电表面上吸附,其活性位和电子转移通道分别为朝向溶液和靠近表面,而纤维素酶则在带正电表面上取得较优的吸附取向。本文研究结果可为工业用酶以合理的取向在载体材料表面固定化提供一定的指导。
利用酶固定化技術來對生物質髮酵穫取生物能源已顯得日益重要。酶與錶麵間的相互作用彊烈影響固定化酶的取嚮,進而影響催化效率。本文採用併行退火矇特卡洛(PTMC)方法對三種生物能源用酶(脂肪酶、纖維素酶和氫化酶)在不同的帶電錶麵和離子彊度下的吸附取嚮進行瞭模擬研究。模擬結果髮現三種酶的吸附主要由靜電吸引力主導,併且很大程度上與蛋白錶麵帶電氨基痠的分佈和溶液離子的靜電屏蔽有關。脂肪酶和氫化酶在帶負電錶麵上吸附,其活性位和電子轉移通道分彆為朝嚮溶液和靠近錶麵,而纖維素酶則在帶正電錶麵上取得較優的吸附取嚮。本文研究結果可為工業用酶以閤理的取嚮在載體材料錶麵固定化提供一定的指導。
이용매고정화기술래대생물질발효획취생물능원이현득일익중요。매여표면간적상호작용강렬영향고정화매적취향,진이영향최화효솔。본문채용병행퇴화몽특잡락(PTMC)방법대삼충생물능원용매(지방매、섬유소매화경화매)재불동적대전표면화리자강도하적흡부취향진행료모의연구。모의결과발현삼충매적흡부주요유정전흡인력주도,병차흔대정도상여단백표면대전안기산적분포화용액리자적정전병폐유관。지방매화경화매재대부전표면상흡부,기활성위화전자전이통도분별위조향용액화고근표면,이섬유소매칙재대정전표면상취득교우적흡부취향。본문연구결과가위공업용매이합리적취향재재체재료표면고정화제공일정적지도。
It is becoming increasingly important to get bioenergy from biomass with enzyme immobilization technology. The interactions between enzymes and carrier surfaces strongly influence the orientation of the immobilized enzymes and thereby affect catalytic efficiency. In this work, Parallel Tempering Monte Carlo (PTMC) simulations were performed to study the adsorption orientations of three kinds of bioenergy-related enzymes (lipase, cellobiohydrolase and hydrogenase) on different electrically charged surfaces and under different solution ionic strength conditions. Simulation results showed that the adsorption of the three enzymes was dominated by electrostatic interactions, and largely relied on the distribution of charged surface amino acids and the screening effect from ions in the solution. It was also found that lipase and hydrogenase adsorbed on negatively charged surface with the active sites toward the solution and the electron transfer channel close to the surface, respectively; while cellobiohydrolase took a preferred orientation on the positively charged surface. This work will provide some guidance for immobilization of industrial enzymes on carrier materials with proper orientation.