A multi-enzyme cascade reaction for the production of L-homophenylalanine
Author:
  • Article
  • | |
  • Metrics
  • |
  • Reference [29]
  • |
  • Related [20]
  • | | |
  • Comments
    Abstract:

    [Objective] L-homophenylalanine (L-HPA) is a key intermediate for many pharmaceuticals and pesticides. As chemical synthesis of L-HPA was complicated and environmentally unfriendly, this study aimed to develop an efficient and environmentally friendly route for the biosynthesis of L-HPA.[Methods] A multi-enzyme cascade reaction for L-HPA production from L-glycine and phenylacetaldehyde was constructed by modular assembly method.[Results] Firstly, the multi-enzyme cascade reaction, which consisted of threonine aldolases (TA), threonine deaminase (TD), phenylalanine dehydrogenase (PheDH), and formate dehydrogenase (FDH), was constructed by literature mining. Then, according to the introduction and deletion of chiral -OH/-NH2 groups, the whole cascade reaction was divided into two parts, in which the basic parts included TA and TD and the extender parts included PheDH and FDH. Next, the two modules were assembled and optimized with different plasmids, enhancing the L-HPA production up to 208.6 mg/L in the optimal engineered strain BL21-C-M1-R-M2. Finally, the whole cell catalytic system was optimized to improve the L-HPA production up to 1226.6 mg/L and the molar conversion of phenylacetaldehyde reached 34.2%.[Conclusion] This environmental-friendly and efficient process represented a promising strategy for large-scale L-HPA production in the future.

    Reference
    [1] Ahmad AL, Oh PC, Abd Shukor SR. Sustainable biocatalytic synthesis of L-homophenylalanine as pharmaceutical drug precursor. Biotechnology Advances, 2009, 27(3):286-296.
    [2] Cho BK, Seo JH, Kang TW, Kim BG. Asymmetric synthesis of L-homophenylalanine by equilibrium-shift using recombinant aromatic L-amino acid transaminase. Biotechnology and Bioengineering, 2003, 83(2):226-234.
    [3] Ding R, Ma R, Ao YH. An analysis on L-phenylalanine industry at home. Fine and Specialty Chemicals, 2011, 19(7):1-3. (in Chinese) 丁锐, 马蓉, 敖永华. 国内L-苯丙氨酸产业浅析. 精细与专用化学品, 2011, 19(7):1-3.
    [4] Wyvratt MJ. Evolution of angiotensin-converting enzyme inhibitors. Clinical Physiology and Biochemistry, 1988, 6(3/4):217-229.
    [5] Ahmad AL, Oh PC, Abd Shukor SR. Sustainable biocatalytic synthesis of L-homophenylalanine as pharmaceutical drug precursor. Biotechnology Advances, 2009, 27(3):286-296.
    [6] Zamai L. The Yin and Yang of ACE/ACE2 pathways:the rationale for the use of renin-angiotensin system inhibitors in COVID-19 patients. Cells, 2020, 9(7):1704.
    [7] Heuson E, Petit JL, Debard A, Job A, Charmantray F, de Berardinis V, Gefflaut T. Continuous colorimetric screening assays for the detection of specific l-or d-α-amino acid transaminases in enzyme libraries. Applied Microbiology and Biotechnology, 2016, 100(1):397-408.
    [8] Luo CH, Lin QM, Lin SY, Meng C, Wang H. Cosynthesis of l-homophenylalanine and 2-phenylethanol by recombinant Saccharomyces cerevisiae expressing aspartate aminotransferase from Escherichia coli BL21(DE3). Journal of Bioscience and Bioengineering, 2017, 123(1):1-7.
    [9] Wang YQ, Zhang H, Lu XY, Zong H, Zhuge B. Advances in 2-phenylethanol production from engineered microorganisms. Biotechnology Advances, 2019, 37(3):403-409.
    [10] Zhang T, Xu SL, Li JH. Study on a new process for the synthesis of homophenylalanine. Journal of Zhejiang University of Technology, 2011, 39(3):264-267. (in Chinese) 张婷, 徐时良, 李景华. 高苯丙氨酸的合成新工艺研究. 浙江工业大学学报, 2011, 39(3):264-267.
    [11] Song W, Chen XL, Wu J, Xu JZ, Zhang WG, Liu J, Chen J, Liu LM. Biocatalytic derivatization of proteinogenic amino acids for fine chemicals. Biotechnology Advances, 2020, 40:107496.
    [12] Song W, Wang JH, Wu J, Liu J, Chen XL, Liu LM. Asymmetric assembly of high-value α-functionalized organic acids using a biocatalytic chiral-group-resetting process. Nature Communications, 2018, 9(1):1-9.
    [13] 宋伟. 多酶级联转化甘氨酸生产α-功能化有机酸的研究. 江南大学博士学位论文, 2019.
    [14] Lo HH, Kao CH, Lee DS, Yang TK, Hsu WH. Enantioselective synthesis of (S)-2-amino-4-phenylbutanoic acid by the hydantoinase method. Chirality, 2003, 15(8):699-702.
    [15] Wang YM, Ban R, Liu L, Shen Y. Construction of recombinant Bacillus subtilis by co-expression of heterologous D-hydantoinase and N-carbamoylase. Acta Microbiologica Sinica, 2017, 57(1):54-65. (in Chinese) 王亚盟, 班睿, 刘露, 申雨. 异源D-海因酶和N-氨甲酰水解酶共表达重组枯草芽孢杆菌的构建. 微生物学报, 2017, 57(1):54-65.
    [16] Chen ST, Tseng MJ, Sookkheo B. Facile synthesis of L-homophenylalanine by equilibrium shift enzymatic reaction using engineered tyrosine aminotransferase. US:6146859. 2000-11-14.
    [17] Li ZQ, Wang XY, Lou XY, Liu BY, Zhang L, You S. Synthesis of L-homophenylalanine by tyrosine aminotransferase method. Journal of Shenyang Pharmaceutical University, 2013, 30(5):399-402, 408. (in Chinese) 李志强, 王潇莹, 娄晓月, 刘冰滢, 张朗, 游松. 酪氨酸转氨酶法制备L-高苯丙氨酸. 沈阳药科大学学报, 2013, 30(5):399-402, 408.
    [18] Chen X, Gao XZ, Zhu DM. Catalysis, engineering and application of amino acid dehydrogenases. Acta Microbiologica Sinica, 2017, 57(8):1249-1261. (in Chinese) 陈曦, 高秀珍, 朱敦明. 氨基酸脱氢酶的催化机理、分子改造及合成应用. 微生物学报, 2017, 57(8):1249-1261.
    [19] Li H, Liao JC. Development of an NADPH-dependent homophenylalanine dehydrogenase by protein engineering. ACS Synthetic Biology, 2014, 3(1):13-20.
    [20] Zhang JL, Zhu TY, Wu XR, Chen YJ. Enhancement of biocatalytic efficiency by increasing substrate loading:enzymatic preparation of l-homophenylalanine. Applied Microbiology and Biotechnology, 2013, 97(19):8487-8494.
    [21] Wang JH, Song W, Wu J, Liu J, Chen XL, Liu LM. Efficient production of phenylpropionic acids by an amino-group-transformation biocatalytic cascade. Biotechnology and Bioengineering, 2020, 117(3):614-625.
    [22] Schrittwieser JH, Velikogne S, Hall M, Kroutil W. Artificial biocatalytic linear cascades for preparation of organic molecules. Chemical Reviews, 2018, 118(1):270-348.
    [23] France SP, Hepworth LJ, Turner NJ, Flitsch SL. Constructing biocatalytic cascades:in vitro and in vivo approaches to de novo multi-enzyme pathways. ACS Catalysis, 2017, 7(1):710-724.
    [24] Fesko K, Reisinger C, Steinreiber J, Weber H, Schürmann M, Griengl H. Four types of threonine aldolases:Similarities and differences in kinetics/thermodynamics. Journal of Molecular Catalysis B:Enzymatic, 2008, 52/53:19-26.
    [25] Franz SE, Stewart JD. Threonine aldolases. Advances in Applied Microbiology, 2014, 88:57-101.
    [26] Zhang C, Xing XH. Research progress in cofactor regeneration systems. Chinese Journal of Biotechnology, 2004, 20(6):811-816. (in Chinese) 张翀, 邢新会. 辅酶再生体系的研究进展. 生物工程学报, 2004, 20(6):811-816.
    [27] Zhao HM, van der Donk WA. Regeneration of cofactors for use in biocatalysis. Current Opinion in Biotechnology, 2003, 14(6):583-589.
    [28] Zhang YF, Wang Q, Hess H. Increasing enzyme cascade throughput by pH-engineering the microenvironment of individual enzymes. ACS Catalysis, 2017, 7(3):2047-2051.
    [29] Tan HL, Guo S, Dinh ND, Luo RC, Jin L, Chen CH. Heterogeneous multi-compartmental hydrogel particles as synthetic cells for incompatible tandem reactions. Nature Communications, 2017, 8:663.
    Cited by
    Comments
    Comments
    分享到微博
    Submit
Get Citation

Jia Liu, Wei Song, Liang Guo, Xiulai Chen, Cong Gao, Liming Liu. A multi-enzyme cascade reaction for the production of L-homophenylalanine. [J]. Acta Microbiologica Sinica, 2021, 61(9): 2829-2842

Copy
Share
Article Metrics
  • Abstract:
  • PDF:
  • HTML:
  • Cited by:
History
  • Received:November 12,2020
  • Revised:February 09,2021
  • Online: September 04,2021
Article QR Code