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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.
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页数:15
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