Activity of endophytic fungi in enantioselective biotransformation of chiral amines: New approach for solid-state fermentation

BIOCATALYSIS AND AGRICULTURAL BIOTECHNOLOGY(2023)

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摘要
Oranges are among the most consumed fruits in Brazil, with over 80 million tons production per year. Currently, one of the main uses of orange residues is to supplement animal feeds. However, orange residues can be used in other ways, including for obtaining enzymes. However, for the pyridoxal 5-phosphate (PLP)-dependent enzyme group, which catalyze transamination reactions, no work has been described. The use of orange-peel residues for solid-state fermentation using endophytic microorganisms is a new and interesting approach to produce these enzymes at lower cost compared to the use of purified enzymes associated to PLP co-factor. In the batch process de-veloped in this study, it was possible to achieve a maximum conversion of 49% after 48 h of incu-bation, an enantiomeric excess of 99% (R)-1,2,3,4-tetra-hydro-1-naphthylamine, and productiv-ity of 0.0102 mg biocatalyst.h-1, using the solid enzyme preparation from Alternaria arborescens as biocatalyst. In a continuous-flow system, 51% conversion and >99% ee of (R)-1,2,3,4-tetra-hydro-1-naphthylamine were achieved, with a six-fold increase productivity (0.0625 mg biocatalyst.h-1). We have screened different fungi samples for transaminase activity and we found a hit for solid-state fermentation. The endophytic fungus genetically identified as Alternaria arborescens showed promising results for the transaminase activity on the kinetic resolution of chiral amine blocks. Therefore, along with other improvement of the biocatalytic toolbox for chi-ral amines synthesis, we have found that the solid enzymatic preparation of the endophytic fun-gus Alternaria arborescens could accept bulky substrates with reasonable activity, compared to the wild-type transaminase already published over literature, and, with high enantioselectivity.
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关键词
Continuous-flow system, Endophytic fungi, Orange peel, rac-1, 2, 3, 4-tetra-hydro-1-naphthylamine, Transamination reaction
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