糖基化
化学
阿卡汀
皮克林乳液
基质(水族馆)
组合化学
肽
乳状液
催化作用
糖苷
有机化学
生物化学
生物
抗氧化剂
芹菜素
类黄酮
生态学
作者
Peng Zhang,Zhe Dong,Shuaiqi Meng,Zhongyu Li,Yu Ji,Ulrich Schwaneberg
标识
DOI:10.1002/anie.202500834
摘要
Pickering emulsion systems are an advanced platform for efficient fine chemical production in biphasic enzymatic catalysis, while their applications are currently limited to a few commercial enzyme classes. Herein, we designed an anchor peptide-based immobilization strategy for Pickering emulsions to achieve efficient glycosylation of natural products by glycosyltransferases (GTs). Firstly, through enzyme mining, natural GTs were utilized to synthesize pharmaceutically important acacetin glucoside and galactoside. However, the best-performing enzymes, BacGT and BarGT-3, still showed low conversions for acacetin glucoside (<40%) and galactoside (<10%). Then, Spy chemistry was employed to cyclize these two GTs (Spy_BacGT and Spy_BarGT-3) for improved robustness, and a Pickering emulsion was formed with the free two Spy_GTs, using 20% 2-hexanone and 1% mesoporous silica nanoparticles (CM), achieving 70% and 66% conversions of acacetin glucoside and galactoside, respectively. Further immobilization of the cyclized GTs onto CM via the anchor peptide LCI (Spy_BacGT/BarGT-3_LCI@CM) further enabled the system to reach more than 90% conversions of acacetin glycosides, retaining 90% conversions after 6-8 cycles. Moreover, this strategy was applied to GTs exhibiting substrate selectivity, achieving efficient non-selective catalysis. This study provides a simple and efficient immobilization strategy to broaden the applications of the Pickering emulsion system in enzymatic glycosylation.
科研通智能强力驱动
Strongly Powered by AbleSci AI