Literature DB >> 21398491

Novel tandem biotransformation process for the biosynthesis of a novel compound, 4-(2,3,5,6-tetramethylpyrazine-1)-4'-demethylepipodophyllotoxin.

Ya-Jie Tang1, Wei Zhao, Hong-Mei Li.   

Abstract

According to the structure of podophyllotoxin and its structure-function relationship, a novel tandem biotransformation process was developed for the directional modification of the podophyllotoxin structure to directionally synthesize a novel compound, 4-(2,3,5,6-tetramethylpyrazine-1)-4'-demethylepipodophyllotoxin (4-TMP-DMEP). In this novel tandem biotransformation process, the starting substrate of podophyllotoxin was biotransformed into 4'-demethylepipodophyllotoxin (product 1) with the demethylation of the methoxyl group at the 4' position by Gibberella fujikuroi SH-f13, which was screened out from Shennongjia prime forest humus soil (Hubei, China). 4'-Demethylepipodophyllotoxin (product 1) was then biotransformed into 4'-demethylpodophyllotoxone (product 2) with the oxidation of the hydroxyl group at the 4 position by Alternaria alternata S-f6, which was screened out from the gathered Dysosma versipellis plants in the Wuhan Botanical Garden, Chinese Academy of Sciences. Finally, 4'-demethylpodophyllotoxone (product 2) and ligustrazine were linked with a transamination reaction to synthesize the target product 4-TMP-DMEP (product 3) by Alternaria alternata S-f6. Compared with podophyllotoxin (i.e., a 50% effective concentration [EC(50)] of 529 μM), the EC(50) of 4-TMP-DMEP against the tumor cell line BGC-823 (i.e., 0.11 μM) was significantly reduced by 5,199 times. Simultaneously, the EC(50) of 4-TMP-DMEP against the normal human proximal tubular epithelial cell line HK-2 (i.e., 0.40 μM) was 66 times higher than that of podophyllotoxin (i.e., 0.006 μM). Furthermore, compared with podophyllotoxin (i.e., log P = 0.34), the water solubility of 4-TMP-DMEP (i.e., log P = 0.66) was significantly enhanced by 94%. For the first time, the novel compound 4-TMP-DMEP with superior antitumor activity was directionally synthesized from podophyllotoxin by the novel tandem biotransformation process developed in this work.

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Year:  2011        PMID: 21398491      PMCID: PMC3126428          DOI: 10.1128/AEM.03047-10

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  26 in total

Review 1.  Target-oriented and diversity-oriented organic synthesis in drug discovery.

Authors:  S L Schreiber
Journal:  Science       Date:  2000-03-17       Impact factor: 47.728

Review 2.  Whole organism biocatalysis.

Authors:  Takeru Ishige; Kohsuke Honda; Sakayu Shimizu
Journal:  Curr Opin Chem Biol       Date:  2005-04       Impact factor: 8.822

Review 3.  Impact of natural products on developing new anti-cancer agents.

Authors:  Gordon M Cragg; Paul G Grothaus; David J Newman
Journal:  Chem Rev       Date:  2009-07       Impact factor: 60.622

Review 4.  Antitumor properties of podophyllotoxin and related compounds.

Authors:  M Gordaliza; M A Castro; J M del Corral; A S Feliciano
Journal:  Curr Pharm Des       Date:  2000-12       Impact factor: 3.116

Review 5.  Podophyllotoxin.

Authors:  C Canel; R M Moraes; F E Dayan; D Ferreira
Journal:  Phytochemistry       Date:  2000-05       Impact factor: 4.072

6.  [Partial synthesis of 4'-demethylepipodophyllotoxin].

Authors:  M Kuhn; C Keller-Juslén; A von Wartburg
Journal:  Helv Chim Acta       Date:  1969       Impact factor: 2.164

7.  Quantitative response of cell growth and Tuber polysaccharides biosynthesis by medicinal mushroom Chinese truffle Tuber sinense to metal ion in culture medium.

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Journal:  Bioresour Technol       Date:  2008-03-18       Impact factor: 9.642

8.  Novel 4 beta-anilino-podophyllotoxin derivatives: design synthesis and biological evaluation as potent DNA-topoisomerase II poisons and anti-MDR agents.

Authors:  Chunqi Hu; Danqing Xu; Wenting Du; Shijing Qian; Li Wang; Jianshu Lou; Qiaojun He; Bo Yang; Yongzhou Hu
Journal:  Mol Biosyst       Date:  2009-12-01

9.  A novel biotransformation process of 4'-demethylepipodophyllotoxin to 4'-demethylepipodophyllic acid by Bacillus fusiformis CICC 20463, Part II: process optimization.

Authors:  Ya-Jie Tang; Xiao-Ling Xu; Jian-Jiang Zhong
Journal:  Bioprocess Biosyst Eng       Date:  2009-04-25       Impact factor: 3.210

10.  Novel biotransformation process of podophyllotoxin to produce podophyllic acid and picropodophyllotoxin by Pseudomonas aeruginosa CCTCC AB93066. Part I: process development.

Authors:  Ya-Jie Tang; Yan Li; Jian-Jiang Zhong
Journal:  Bioprocess Biosyst Eng       Date:  2008-12-30       Impact factor: 3.210

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  3 in total

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Journal:  J Inflamm Res       Date:  2022-08-15

2.  An Alkylpyrazine Synthesis Mechanism Involving l-Threonine-3-Dehydrogenase Describes the Production of 2,5-Dimethylpyrazine and 2,3,5-Trimethylpyrazine by Bacillus subtilis.

Authors:  Lijie Zhang; Yanli Cao; Jianan Tong; Yan Xu
Journal:  Appl Environ Microbiol       Date:  2019-11-27       Impact factor: 4.792

3.  Discovery of Novel c-Jun N-Terminal Kinase 1 Inhibitors from Natural Products: Integrating Artificial Intelligence with Structure-Based Virtual Screening and Biological Evaluation.

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Journal:  Molecules       Date:  2022-09-22       Impact factor: 4.927

  3 in total

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