化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2014年
9期
3583-3591
,共9页
万丽花%姚忠%倪芳%韦敏%周治%王浩绮%孙芸%仲兆祥
萬麗花%姚忠%倪芳%韋敏%週治%王浩綺%孫蕓%仲兆祥
만려화%요충%예방%위민%주치%왕호기%손예%중조상
栀子苷%β-葡萄糖苷酶%京尼平%两相体系%催化
梔子苷%β-葡萄糖苷酶%京尼平%兩相體繫%催化
치자감%β-포도당감매%경니평%량상체계%최화
gardenoside%β-glucosidase%genipin%two phase medium%catalysis
京尼平是一种天然生物交联剂,且具有多种生理活性。本文以β-葡萄糖苷酶催化栀子苷水解制备京尼平为目标体系,证明了京尼平对β-D-葡萄糖苷酶具有竞争性抑制作用;考察了β-D-葡萄糖苷酶在不同有机相-水体系中的稳定性,发现其在正辛醇-水、正己醇-水体系中的稳定性均较好;测定了栀子苷在正辛醇-水和正己醇-水体系中的分配系数kD,gardenoside分别为0.17和0.76,而京尼平的分配系数kD,genipin为42.57和37.75;分别在水、正辛醇-水和正己醇-水体系中进行栀子苷水解制备京尼平的反应,当底物浓度为0.25μmol·ml-1时京尼平收率分别为89.17%、93.96%、90.16%;进一步提高底物浓度为2.0μmol·ml-1时,正辛醇-水体系中京尼平收率高达91.9%,较水相体系(79.7%)提高了12.2%。本文的研究结果证明了采用正辛醇-水两相反应体系可部分解除产物抑制,提高产物收率,并简化后续的产物分离。
京尼平是一種天然生物交聯劑,且具有多種生理活性。本文以β-葡萄糖苷酶催化梔子苷水解製備京尼平為目標體繫,證明瞭京尼平對β-D-葡萄糖苷酶具有競爭性抑製作用;攷察瞭β-D-葡萄糖苷酶在不同有機相-水體繫中的穩定性,髮現其在正辛醇-水、正己醇-水體繫中的穩定性均較好;測定瞭梔子苷在正辛醇-水和正己醇-水體繫中的分配繫數kD,gardenoside分彆為0.17和0.76,而京尼平的分配繫數kD,genipin為42.57和37.75;分彆在水、正辛醇-水和正己醇-水體繫中進行梔子苷水解製備京尼平的反應,噹底物濃度為0.25μmol·ml-1時京尼平收率分彆為89.17%、93.96%、90.16%;進一步提高底物濃度為2.0μmol·ml-1時,正辛醇-水體繫中京尼平收率高達91.9%,較水相體繫(79.7%)提高瞭12.2%。本文的研究結果證明瞭採用正辛醇-水兩相反應體繫可部分解除產物抑製,提高產物收率,併簡化後續的產物分離。
경니평시일충천연생물교련제,차구유다충생리활성。본문이β-포도당감매최화치자감수해제비경니평위목표체계,증명료경니평대β-D-포도당감매구유경쟁성억제작용;고찰료β-D-포도당감매재불동유궤상-수체계중적은정성,발현기재정신순-수、정기순-수체계중적은정성균교호;측정료치자감재정신순-수화정기순-수체계중적분배계수kD,gardenoside분별위0.17화0.76,이경니평적분배계수kD,genipin위42.57화37.75;분별재수、정신순-수화정기순-수체계중진행치자감수해제비경니평적반응,당저물농도위0.25μmol·ml-1시경니평수솔분별위89.17%、93.96%、90.16%;진일보제고저물농도위2.0μmol·ml-1시,정신순-수체계중경니평수솔고체91.9%,교수상체계(79.7%)제고료12.2%。본문적연구결과증명료채용정신순-수량상반응체계가부분해제산물억제,제고산물수솔,병간화후속적산물분리。
Genipin is an important bio-crosslinking agent with multiple physiological activities. In this paper, the competitive inhibition for activity ofβ-glucosidase by genipin was demonstrated. The stabilities ofβ-glucosidase in different organic solvents were investigated. Stability ofβ-glucosidase was satisfactory in the octanol-water and hexanol-water medium. The partition coefficients for gardenoside in the octanol-water and hexanol-water system were 0.17 and 0.76, while those for genipin were 42.57 and 37.75 respectively. The process for preparation of genipin was carried out in water, octanol-water and hexanol-water respectively, while gardenoside concentration was 0.25μmol·ml-1. The obtained genipin yields were 89.17%, 93.96%and 90.16%respectively. Furthermore, the effect of gardenoside concentration on genipin yield was also investigated. While in the octanol-water system, conversion rate of genipin was as high as 91.9%at the gardenoside concentration of 2.0μmol·ml-1, an increase of 12.2%compared to that in water. Using the octanol-water medium was helpful for partially eliminating product inhibition, improving genipin yield and simplifying product recovery.