Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory

Abstract Background d-Amino acids are increasingly used as building blocks to produce pharmaceuticals and fine chemicals. However, establishing a universal biocatalyst for the general synthesis of d-amino acids from cheap and readily available precursors with few by-products is challenging. In this...

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Main Authors: Dan-Ping Zhang, Xiao-Ran Jing, Lun-Jie Wu, An-Wen Fan, Yao Nie, Yan Xu
Format: Article
Language:English
Published: BMC 2021-01-01
Series:Microbial Cell Factories
Subjects:
Online Access:https://doi.org/10.1186/s12934-020-01506-x
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spelling doaj-d9d45a4f2300470192db14afe07ea7002021-01-10T12:42:10ZengBMCMicrobial Cell Factories1475-28592021-01-0120111310.1186/s12934-020-01506-xHighly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factoryDan-Ping Zhang0Xiao-Ran Jing1Lun-Jie Wu2An-Wen Fan3Yao Nie4Yan Xu5School of Biotechnology and Key laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan UniversitySchool of Biotechnology and Key laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan UniversitySchool of Biotechnology and Key laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan UniversitySchool of Biotechnology and Key laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan UniversitySchool of Biotechnology and Key laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan UniversitySchool of Biotechnology and Key laboratory of Industrial Biotechnology, Ministry of Education, Jiangnan UniversityAbstract Background d-Amino acids are increasingly used as building blocks to produce pharmaceuticals and fine chemicals. However, establishing a universal biocatalyst for the general synthesis of d-amino acids from cheap and readily available precursors with few by-products is challenging. In this study, we developed an efficient in vivo biocatalysis system for the synthesis of d-amino acids from l-amino acids by the co-expression of membrane-associated l-amino acid deaminase obtained from Proteus mirabilis (LAAD), meso-diaminopimelate dehydrogenases obtained from Symbiobacterium thermophilum (DAPDH), and formate dehydrogenase obtained from Burkholderia stabilis (FDH), in recombinant Escherichia coli. Results To generate the in vivo cascade system, three strategies were evaluated to regulate enzyme expression levels, including single-plasmid co-expression, double-plasmid co-expression, and double-plasmid MBP-fused co-expression. The double-plasmid MBP-fused co-expression strain Escherichia coli pET-21b-MBP-laad/pET-28a-dapdh-fdh, exhibiting high catalytic efficiency, was selected. Under optimal conditions, 75 mg/mL of E. coli pET-21b-MBP-laad/pET-28a-dapdh-fdh whole-cell biocatalyst asymmetrically catalyzed the stereoinversion of 150 mM l-Phe to d-Phe, with quantitative yields of over 99% ee in 24 h, by the addition of 15 mM NADP+ and 300 mM ammonium formate. In addition, the whole-cell biocatalyst was used to successfully stereoinvert a variety of aromatic and aliphatic l-amino acids to their corresponding d-amino acids. Conclusions The newly constructed in vivo cascade biocatalysis system was effective for the highly selective synthesis of d-amino acids via stereoinversion.https://doi.org/10.1186/s12934-020-01506-xd-amino acidsIn vivoCascadeWhole-cell biocatalysisStereoinversionSelectivity
collection DOAJ
language English
format Article
sources DOAJ
author Dan-Ping Zhang
Xiao-Ran Jing
Lun-Jie Wu
An-Wen Fan
Yao Nie
Yan Xu
spellingShingle Dan-Ping Zhang
Xiao-Ran Jing
Lun-Jie Wu
An-Wen Fan
Yao Nie
Yan Xu
Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory
Microbial Cell Factories
d-amino acids
In vivo
Cascade
Whole-cell biocatalysis
Stereoinversion
Selectivity
author_facet Dan-Ping Zhang
Xiao-Ran Jing
Lun-Jie Wu
An-Wen Fan
Yao Nie
Yan Xu
author_sort Dan-Ping Zhang
title Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory
title_short Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory
title_full Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory
title_fullStr Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory
title_full_unstemmed Highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory
title_sort highly selective synthesis of d-amino acids via stereoinversion of corresponding counterpart by an in vivo cascade cell factory
publisher BMC
series Microbial Cell Factories
issn 1475-2859
publishDate 2021-01-01
description Abstract Background d-Amino acids are increasingly used as building blocks to produce pharmaceuticals and fine chemicals. However, establishing a universal biocatalyst for the general synthesis of d-amino acids from cheap and readily available precursors with few by-products is challenging. In this study, we developed an efficient in vivo biocatalysis system for the synthesis of d-amino acids from l-amino acids by the co-expression of membrane-associated l-amino acid deaminase obtained from Proteus mirabilis (LAAD), meso-diaminopimelate dehydrogenases obtained from Symbiobacterium thermophilum (DAPDH), and formate dehydrogenase obtained from Burkholderia stabilis (FDH), in recombinant Escherichia coli. Results To generate the in vivo cascade system, three strategies were evaluated to regulate enzyme expression levels, including single-plasmid co-expression, double-plasmid co-expression, and double-plasmid MBP-fused co-expression. The double-plasmid MBP-fused co-expression strain Escherichia coli pET-21b-MBP-laad/pET-28a-dapdh-fdh, exhibiting high catalytic efficiency, was selected. Under optimal conditions, 75 mg/mL of E. coli pET-21b-MBP-laad/pET-28a-dapdh-fdh whole-cell biocatalyst asymmetrically catalyzed the stereoinversion of 150 mM l-Phe to d-Phe, with quantitative yields of over 99% ee in 24 h, by the addition of 15 mM NADP+ and 300 mM ammonium formate. In addition, the whole-cell biocatalyst was used to successfully stereoinvert a variety of aromatic and aliphatic l-amino acids to their corresponding d-amino acids. Conclusions The newly constructed in vivo cascade biocatalysis system was effective for the highly selective synthesis of d-amino acids via stereoinversion.
topic d-amino acids
In vivo
Cascade
Whole-cell biocatalysis
Stereoinversion
Selectivity
url https://doi.org/10.1186/s12934-020-01506-x
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