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Enzymatic Synthesis of Resveratrol α-Glucoside by Amylosucrase of Deinococcus geothermalis 원문보기

Journal of microbiology and biotechnology, v.31 no.12, 2021년, pp.1692 - 1700  

Moon, Keumok (Microbiological Resource Research Institute, Pusan National University) ,  Lee, Seola (Department of Microbiology, Pusan National University) ,  Park, Hyunsu (Department of Microbiology, Pusan National University) ,  Cha, Jaeho (Microbiological Resource Research Institute, Pusan National University)

Abstract AI-Helper 아이콘AI-Helper

Glycosylation of resveratrol was carried out by using the amylosucrase of Deinococcus geothermalis, and the glycosylated products were tested for their solubility, chemical stability, and biological activities. We synthesized and identified these two major glycosylated products as resveratrol-4'-O-&...

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참고문헌 (44)

  1. 1 Constant J 1997 Alcohol, ischemic heart disease, and the French paradox Clin. Cardiol. 20 420 424 10.1002/clc.4960200504 9134271 

  2. 2 Fan E Zhang L Jiang S Bai Y 2008 Beneficial effects of resveratrol on atherosclerosis J. Med. Food. 11 610 614 10.1089/jmf.2007.0091 19053850 

  3. 3 Su D Cheng Y Liu M Liu D Cui H Zhang B 2013 Comparision of piceid and resveratrol in antioxidation and antiproliferation activities in vitro PLoS One 8 e54505 10.1371/journal.pone.0054505 23342161 

  4. 4 Jang M Cai L Udeani GO Slowing KV Thomas CF Beecher CWW 1997 Cancer chemopreventive activity of resveratrol, a natural product derived from grapes Science 275 218 220 10.1126/science.275.5297.218 8985016 

  5. 5 Mizutani K Ikeda K Kawai Y Yamori Y 1998 Resveratrol stimulates the proliferation and differentiation of osteoblastic MC3T3-E1 cells Biochem. Biophys. Res. Commun. 253 859 863 10.1006/bbrc.1998.9870 9918820 

  6. 6 Newton RA Cook AL Roberts DW Leonard JH Sturm RA 2007 Post-transcriptional regulation of melanin biosynthetic enzymes by cAMP and resveratrol in human melanocytes J. Invest. Dermatol. 127 2216 2227 10.1038/sj.jid.5700840 17460731 

  7. 7 Fremont L 2000 Biological effects of resveratrol Life Sci. 66 663 673 10.1016/S0024-3205(99)00410-5 10680575 

  8. 8 Baxter RA 2008 Anti-aging properties of resveratrol: review and report of a potent new antioxidant skin care formulation J. Cosmet. Dermatol. 7 2 7 10.1111/j.1473-2165.2008.00354.x 18254804 

  9. 9 Chimento A De Amicis F Sirianni R Sinicropi MS Puoci F Casaburi I 2019 Progress to improve oral bioavailability and beneficial effects of resveratrol Int. J. Mol. Sci. 20 1381 10.3390/ijms20061381 30893846 

  10. 10 Walle T 2011 Bioavailability of resveratrol Ann. NY Acad. Sci. 1215 9 15 10.1111/j.1749-6632.2010.05842.x 21261636 

  11. 11 Walle T Hsieh F DeLegge MH Oatis JE Walle UK 2004 High absorption but very low bioavailability of oral resveratrol in humans Drug Metab. Dispos. 32 1377 1382 10.1124/dmd.104.000885 15333514 

  12. 12 Yu C Shin YG Chow A Li Y Kosmeder JW Lee YS 2002 Human, rat, and mouse metabolism of resveratrol Pharm. Res. 19 1907 1914 10.1023/A:1021414129280 12523673 

  13. 13 Wenzel E Somoza V 2005 Metabolism and bioavailability of trans -resveratrol Mol. Nutr. Food Res. 49 472 481 10.1002/mnfr.200500010 15779070 

  14. 14 Orsini F Verotta L Klimo K Gerhäuser C 2016 Synthesis of resveratrol derivatives and in vitro screening for potential cancer chemopreventive activities Arch. Pharm. Chem. Life Sci. 349 414 427 10.1002/ardp.201600022 27159630 

  15. 15 Liu Q Kim C Jo YH Kim SB Hwang BY Lee MK 2015 Synthesis and biological evaluation of resveratrol derivatives as melanogenesis inhibitors Molecules 20 16933 16945 10.3390/molecules200916933 26393543 

  16. 16 Cho HK Kim HH Seo DH Jung JH Park JH Baek NI 2011 Biosynthesis of (+) − catechin glycosides using recombinant amylosucrase from Deinococcus geothermalis DSM 11300 Enzyme Microb. Technol. 49 246 253 10.1016/j.enzmictec.2011.05.007 22112416 

  17. 17 Moon KO Park H Joo M Ha KT Baek NI Park CS 2017 Glycosylation enhances the physicochemical properties of caffeic acid phenethyl ester J. Microbiol. Biotechnol. 27 1916 1924 10.4014/jmb.1706.06017 28870007 

  18. 18 Park S Moon K Park CS Jung DH Cha J 2018 Synthesis of aesculetin and aesculin glycosides using engineered Escherichia coli expressing Neisseria polysaccharea amylosucrase J. Microbiol. Biotechnol. 28 566 570 10.4014/jmb.1711.11055 29724082 

  19. 19 Kim KH Park YD Park H Moon KO Ha KT Baek NI 2014 Synthesis and biological evaluation of a novel baicalein glycoside as an anti-inflammatory agent Eur. J. Pharmacol. 744 147 156 10.1016/j.ejphar.2014.10.013 25446915 

  20. 20 Kometani T Nishimura T Nakae T Takii H Okada S 1996 Synthesis of neohesperidin glycosides and naringin glycosides by cyclodextrin glucano-transferase from an Alkalophilic Bacillus species Biosci. Biotechnol. Biochem. 60 645 649 10.1271/bbb.60.645 8829532 

  21. 21 Jung JH Seo DH Ha SJ Song MC Cha J Yoo SH 2009 Enzymatic synthesis of salicin glycosides through transglycosylation catalyzed by amylosucrases from Deinococcus geothermalis and Neisseria polysaccharea Carbohydr. Res. 344 1612 1619 10.1016/j.carres.2009.04.019 19482267 

  22. 22 Park H Kim J Choi KH Hwang S Yang SJ Baek NI 2012 Enzymatic synthesis of piceid glucosides using maltosyltransferase from Caldicellulosiruptor bescii DSM 6725 J. Agric. Food Chem. 60 8183 8189 10.1021/jf302127a 22823185 

  23. 23 Regev-Shoshani G Shoseyov O Bilkis I Kerem Z 2003 Glycosylation of resveratrol protects it from enzymic oxidation Biochem. J. 374 157 163 10.1042/bj20030141 12697026 

  24. 24 Moon K Cha J 2020 Enhancement of antioxidant and antibacterial activities of Salvia miltiorrhiza roots fermented with Aspergillus oryzae Foods 9 34 10.3390/foods9010034 31906298 

  25. 25 Park HJ Lee EH Jung HY Kang IK Cho YJ 2020 Effects of phenolics from Oplismenus undulatifolius in α-MSH-stimulated B16F10 melanoma cells J. Appl. Biol. Chem. 63 89 93 10.3839/jabc.2020.012 

  26. 26 Marier JF Vachon P Gritsas A Zhang J Moreau JP Ducharme MP 2002 Metabolism and disposition of resveratrol in rats: extent of absorption, glucuronidation, and enterohepatic recirculation evidenced by a linked-rat model J. Pharmacol. Exp. Ther. 302 369 373 10.1124/jpet.102.033340 12065739 

  27. 27 Remsberg CM Yáñez JA Ohgami Y Vega‐Villa KR Rimando AM Davies NM 2008 Pharmacometrics of pterostilbene: preclinical pharmacokinetics and metabolism, anticancer, antiinflammatory, antioxidant and analgesic activity Phytother. Res. 22 169 179 10.1002/ptr.2277 17726731 

  28. 28 Thaipong K Boonprakob U Crosby K Cisneros-Zevallos L Byrne DH 2006 Comparison of ABTS, DPPH, FRAP, and ORAC assays for estimating antioxidant activity from guava fruit extracts J. Food Compos. Anal. 19 669 675 10.1016/j.jfca.2006.01.003 

  29. 29 Jun SY Park KM Choi KW Jang MK Kang HY Lee SH 2008 Inhibitory effects of arbutin-β-glycosides synthesized from enzymatic transglycosylation for melanogenesis Biotechnol. Lett. 30 743 748 10.1007/s10529-007-9605-1 18040603 

  30. 30 Lee TH Seo JO Baek SH Kim SY 2014 Inhibitory effects of resveratrol on melanin synthesis in ultraviolet B-induced pigmentation in Guinea pig skin Biomol. Ther. 22 35 40 10.4062/biomolther.2013.081 24596619 

  31. 31 Yoon HS Hyun CG Lee NH Park SS Shin DB 2016 Comparative depigmentation effects of resveratrol and its two methyl analogues in α-melanocyte stimulating hormone-triggered B16/F10 murine melanoma cells Prev. Nutr. Food Sci. 21 155 10.3746/pnf.2016.21.2.155 27390733 

  32. 32 Kim JK Park KT Lee HS Kim M Lim YH 2012 Evaluation of the inhibition of mushroom tyrosinase and cellular tyrosinase activities of oxyresveratrol: comparison with mulberroside A J. Enzyme Inhib. Med. Chem. 27 495 503 10.3109/14756366.2011.598866 21827364 

  33. 33 Satooka H Kubo I 2012 Resveratrol as a k cat type inhibitor for tyrosinase: potentiated melanogenesis inhibitor Bioorg. Med. Chem. 20 1090 1099 10.1016/j.bmc.2011.11.030 22189272 

  34. 34 Jeong ET Jin MH Kim MS Chang YH Park SG 2010 Inhibition of melanogenesis by piceid isolated from Polygonum cuspidatum Arch. Pharm. Res. 33 1331 1338 10.1007/s12272-010-0906-x 20945131 

  35. 35 Ozaki S Imai H Iwakiri T Sato T Shimoda K Nakayama T 2012 Regioselective glucosidation of trans-resveratrol in Escherichia coli expressing glucosyltransferase from Phytolacca americana Biotechnol. Lett. 34 475 481 10.1007/s10529-011-0784-4 22048846 

  36. 36 Stivala LA Savio M Carafoli F Perucca P Bianchi L Maga G 2001 Specific structural determinants are responsible for the antioxidant activity and the cell cycle effects of resveratrol J. Biol. Chem. 276 22586 22594 10.1074/jbc.M101846200 11316812 

  37. 37 Waffo Teguo P Fauconneau B Deffieux G Huguet F Vercauteren J Mérillon J-M 1998 Isolation, identification, and antioxidant activity of three stilbene glucosides newly extracted from Vitis vinifera cell cultures J. Nat. Prod. 61 655 657 10.1021/np9704819 9599270 

  38. 38 Fang JG Lu M Chen ZH Zhu HH Li Y Yang L 2002 Antioxidant effects of resveratrol and its analogues against the free‐radical‐induced peroxidation of linoleic acid in micelles Chem. Eur. J. 8 4191 4198 10.1002/1521-3765(20020916)8:18<4191::AID-CHEM4191>3.0.CO;2-S 12298009 

  39. 39 Henríquez C López-Alarcón C Lutz MGM Speisky H 2011 Time-dependence of ferric reducing antioxidant power (FRAP) index in Chilean apples and berries Arch. Latinoam. Nutr. 61 323 332 22696902 

  40. 40 Ohguchi K Tanaka T Kido T Baba K Iinuma M Matsumoto K 2003 Effects of hydroxystilbene derivatives on tyrosinase activity Biochem. Biophys. Res. Commun. 307 861 863 10.1016/S0006-291X(03)01284-1 12878190 

  41. 41 Lee HS Lee BW Kim MR Jun JG 2010 Syntheses of resveratrol and its hydroxylated derivatives as radical scavenger and tyrosinase inhibitor Bull. Korean Chem. Soc. 31 971 975 10.5012/bkcs.2010.31.04.971 

  42. 42 Funayama M Arakawa H Yamamoto R Nishino T Shin T Murao S 1995 Effects of α-and β-arbutin on activity of tyrosinases from mushroom and mouse melanoma Biosci. Biotechnol. Biochem. 59 143 144 10.1271/bbb.59.143 7765966 

  43. 43 Yamada M Tanabe F Arai N Mitsuzumi H Miwa Y Kubota M 2006 Bioavailability of glucosyl hesperidin in rats Biosci. Biotechnol. Biochem. 70 1386 1394 10.1271/bbb.50657 16794318 

  44. 44 Jiang JR Yuan S Ding JF Zhu SC Xu HD Chen T 2008 Conversion of puerarin into its 7- O -glycoside derivatives by Microbacterium oxydans (CGMCC 1788) to improve its water solubility and pharmacokinetic properties Appl. Microbiol. Biotechnol. 81 647 657 10.1007/s00253-008-1683-z 18795283 

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