催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2012年
2期
275-280
,共6页
王琴琴%郁蕙蕾%赵娜%李春秀%尚亚卓%刘洪来%许建和
王琴琴%鬱蕙蕾%趙娜%李春秀%尚亞卓%劉洪來%許建和
왕금금%욱혜뢰%조나%리춘수%상아탁%류홍래%허건화
β-D-烷基葡萄糖苷%癸基-D-葡萄糖苷%酶催化%逆水解%微水环境%平衡收率
β-D-烷基葡萄糖苷%癸基-D-葡萄糖苷%酶催化%逆水解%微水環境%平衡收率
β-D-완기포도당감%계기-D-포도당감%매최화%역수해%미수배경%평형수솔
alkyl β-D-glucosides%decyl β-D-glucoside%enzymatic synthesis%reverse hydrolysis%water-poor system%equilibrium yield
使用酶法合成了一系列不同烷基链长的β-D-烷基葡萄糖苷.结果表明,除甲基糖苷外,烷基碳链越长,反应初速度越低,糖苷的最终收率越低.从热力学角度系统地研究了这些糖苷合成的平衡常数和吉布斯自由能变化.通过改变反应的平衡,提高了长链烷基糖苷的最终收率.当水含量从10%降至5% (v/v),使用叔丁醇作为共溶剂,添加0.1 mol/L葡萄糖作为底物时,癸基糖苷的平衡得率从1.9%提高至6.1%.除了其他长链的烷基糖苷外,庚基糖苷也显示了明显的表面活性剂活性.
使用酶法閤成瞭一繫列不同烷基鏈長的β-D-烷基葡萄糖苷.結果錶明,除甲基糖苷外,烷基碳鏈越長,反應初速度越低,糖苷的最終收率越低.從熱力學角度繫統地研究瞭這些糖苷閤成的平衡常數和吉佈斯自由能變化.通過改變反應的平衡,提高瞭長鏈烷基糖苷的最終收率.噹水含量從10%降至5% (v/v),使用叔丁醇作為共溶劑,添加0.1 mol/L葡萄糖作為底物時,癸基糖苷的平衡得率從1.9%提高至6.1%.除瞭其他長鏈的烷基糖苷外,庚基糖苷也顯示瞭明顯的錶麵活性劑活性.
사용매법합성료일계렬불동완기련장적β-D-완기포도당감.결과표명,제갑기당감외,완기탄련월장,반응초속도월저,당감적최종수솔월저.종열역학각도계통지연구료저사당감합성적평형상수화길포사자유능변화.통과개변반응적평형,제고료장련완기당감적최종수솔.당수함량종10%강지5% (v/v),사용숙정순작위공용제,첨가0.1 mol/L포도당작위저물시,계기당감적평형득솔종1.9%제고지6.1%.제료기타장련적완기당감외,경기당감야현시료명현적표면활성제활성.
An array of ten β-D-glucopyranosides with varied alkyl chain lengths were enzymatically synthesized.It was found that for longeralkyl chains a lower initial rate and final yield of glucoside was obtained except for methyl glucoside because of the severe toxicity of methanol to the enzyme.From a thermodynamics point of view,the equilibrium constant and Gibbs free energy variation of the glucoside syntheses were systematically investigated.To improve the final yields of the glucosides containing long alkyl chains the equilibrium of the enzymatic glucoside synthesis was altered.The equilibrium yield of decyl β-D-glucoside increased from 1.9% to 6.1% when the water content was reduced from 10% to 5% (v/v) using tert-butanol as a cosolvent and 0.10 mol/L of glucose as a substrate.As for the other longer alkyl chain glucosides,heptyl β-D-glucoside was found to have significant surface activity as well.