Synthesis of a precursor of D-fagomine by immobilized fructose-6-phosphate aldolase

被引:4
|
作者
Masdeu, Gerard [1 ,4 ]
Miguel Vazquez, Luis [1 ]
Lopez-Santin, Josep [1 ]
Caminal, Gloria [2 ]
Kralj, Slavko [3 ]
Makovec, Darko [3 ]
Alvaro, Gregorio [1 ]
Guillen, Marina [1 ]
机构
[1] Univ Autonoma Barcelona, Dept Chem Biol & Environm Engn, Barcelona, Spain
[2] IAQC CSIC, Inst Adv Chem Catalonia, Barcelona, Spain
[3] Jozef Stefan Inst, Dept Mat Synth, Ljubljana, Slovenia
[4] Chalmers Univ Technol, Dept Chem & Chem Engn, Gothenburg, Sweden
来源
PLOS ONE | 2021年 / 16卷 / 04期
关键词
D-FRUCTOSE-6-PHOSPHATE ALDOLASE; ESCHERICHIA-COLI; NANOPARTICLE CLUSTERS; ENZYMATIC-SYNTHESIS; ORGANIC-SYNTHESIS; ENZYMES; GLYCOLALDEHYDE; MONOOXYGENASE; PURIFICATION; NUCLEOPHILES;
D O I
10.1371/journal.pone.0250513
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fructose-6-phosphate aldolase (FSA) is an important enzyme for the C-C bond-forming reactions in organic synthesis. The present work is focused on the synthesis of a precursor of D-fagomine catalyzed by a mutant FSA. The biocatalyst has been immobilized onto several supports: magnetic nanoparticle clusters (mNC), cobalt-chelated agarose (Co-IDA), amino-functionalized agarose (MANA-agarose) and glyoxal-agarose, obtaining a 29.0%, 93.8%, 89.7% and 53.9% of retained activity, respectively. Glyoxal-agarose FSA derivative stood up as the best option for the synthesis of the precursor of D-fagomine due to the high reaction rate, conversion, yield and operational stability achieved. FSA immobilized in glyoxal-agarose could be reused up to 6 reaction cycles reaching a 4-fold improvement in biocatalyst yield compared to the non-immobilized enzyme.
引用
收藏
页数:15
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