Citation: Yan Yaru, Qi Bowen, Mo Ting, Wang Xiaohui, Wang Juan, Shi Shepo, Liu Xiao, Tu Pengfei. Research Progress of Rhamnosyltransferase[J]. Chinese Journal of Organic Chemistry, ;2018, 38(9): 2281-2295. doi: 10.6023/cjoc201806004 shu

Research Progress of Rhamnosyltransferase

Modern Research Center for Traditional Chinese Medicine, School of Chinese Meteria Medica, Beijing University of Chinese Medicine, Beijing 100029

Corresponding author: Shi Shepo, shishepo@163.com Liu Xiao, fcliuxiao@163.com Tu Pengfei, pengfeitu@163.com
Received Date: 1 June 2018
Revised Date: 10 August 2018
Available Online: 14 September 2018
Fund Project: Project supported by the National Natural Science Foundation of China (No. 81402809) and the Foundation from Beijing University of Chinese Medicine (No. 2018-JYB-XJQ006)the National Natural Science Foundation of China 81402809the Foundation from Beijing University of Chinese Medicine 2018-JYB-XJQ006

Figures(12)

Rhamnosylation is an important type of glycosylation reaction which is widely involved in organic synthesis and structural modification of natural products. In vivo, rhamnosylation is catalyzed by rhamnosyltransferase that transferred the active rhamnosyl donors to the specific sugar acceptors. A larger number of rhamnosyltransferases have been identified in natural and they often played key roles in the biosynthesis of diverse natural products as well as maintaining the cell structure and physiological functions of biological organisms. Besides, enzymatic rhamnosylation has been an effective complementary method to chemical catalysis in the field of organic glycosylation modifications due to its high catalysis efficiency and specificity, mild reaction conditions as well as environment friendship and so on. In this article, research progresses of rhamnosyltransferase are reviewed based on their enzymatic functions, three dimensional structure investigations, rhamnosyl donors' synthesis, enzymatic catalysis promiscuities, and biochemical catalysis applications. Finally, the future development and application of them are also prospected.
- rhamnosyltransferase,
- biosynthesis,
- enzyme catalysis,
- biocatalysis
1. [1]
  Weymouth-Wilson, A. C. Nat. Prod. Rep. 1997, 14, 99. doi: 10.1039/np9971400099
2. [2]
  Aksamit-Stachurska, A.; Korobczak-Sosna, A.; Kulma, A.; Szopa, J. BMC Biotechnol. 2008, 8, 25.
3. [3]
  Wang, J.; Hou, B. K. Plant Physiol. Commun. 2008, 44, 997(in Chinese).
4. [4]
  Jin, Y.; Wu, X. R.; Chen, Y. J. J. China Pharm. Univ. 2017, 48, 529(in Chinese). doi: 10.11665/j.issn.1000-5048.20170504
5. [5]
  Wu, X. M.; Xu, T. T.; Chu, J. L.; He, B. F. Chin. J. Nat. Med. 2010, 8, 389(in Chinese).
6. [6]
  Hayder, N.; Bouhlel, I.; Skandrani, I.; Kadri, M.; Steiman, R.; Guiraud, P.; Mariotte, A. M.; Ghedira, K.; Dijoux-Franca, M. G.; Chekir-Ghedira, L. Toxicol. In Vitro 2008, 22, 567.
7. [7]
  An, J.; Zuo, G. Y.; Hao, X. Y.; Wang, G. C.; Li, Z. S. Phyto-medicine 2011, 18, 990.
8. [8]
  Choi, H. J.; Kim, J. H.; Lee, C. H.; Ahn, Y. J.; Song, J. H.; Baek, S. H.; Kwon, D. H. Antiviral Res. 2009, 81, 77.
9. [9]
  Choi, H. J.; Song, J. H.; Park, K. S.; Kwon, D. H. Eur. J. Pharm. Sci. 2009, 37, 329. doi: 10.1016/j.ejps.2009.03.002
10. [10]
  Rodríguez, P.; González-Mujica, F.; Bermúdez, J.; Hasegawa, M. Fitoterapia 2010, 81, 1220.
11. [11]
  Diantini, A.; Subarnas, A.; Lestari, K.; Halimah, E.; Susilawati, Y.; Supriyatna.; Julaeha, E.; Achmad, T. H.; Suradji, E. W.; Yamazaki, C.; Kobayashi, K.; Koyama, H.; Abdulah, R. Oncol. Lett. 2012, 3, 1069.
12. [12]
  Sharoar, M. G.; Thapa, A.; Shahnawaz, M.; Ramasamy, V. S.; Woo, E. R.; Shin, S. Y.; Park, I. S. J. Biomed. Sci. 2012, 19, 104.
13. [13]
  Holler, J. G.; Christensen, S. B.; Slotved, H. C.; Rasmussen, H. B.; Gúzman, A.; Olsen, C. E.; Petersen, B.; Mølgaard, P. J. An-timicrob. Chemother. 2012, 67, 1138.
14. [14]
  Yin, R.; Han, K.; Heller, W.; Albert, A.; Dobrev, P. I.; Zažímalová, E.; Schäffner, A. R. New Phytol. 2014, 201, 466. doi: 10.1111/nph.12558
15. [15]
  Bols, M.; Binderup, L.; Hansen, J.; Rasmussen, P. J. Med. Chem. 1992, 35, 2768.
16. [16]
  Thibodeaux, C. J.; Melançon, C. E.; Liu, H. W. Angew. Chem., Int. Ed. 2008, 47, 9814.
17. [17]
  Kamiya, S.; Esaki, S.; Hama, M. Agric. Biol. Chem. 1967, 31, 397.
18. [18]
  Nishio, T.; Miyake, Y.; Tsujii, H.; Hakamata, W.; Kadokura, K.; Oku, T. Biosci., Biotechnol., Biochem. 1996, 60, 2038. doi: 10.1271/bbb.60.2038
19. [19]
  Cantarel, B. L.; Coutinho, P. M.; Rancurel, C.; Bernard, T.; Lombard, V.; Henrissat, B. Nucleic Acids Res. 2009, 37, 233.
20. [20]
  Guo, S.; Luo, H. M.; Song, J. Y.; Sun, C.; Chen, S. L. World. Sci. Technol. (Modern. Tradit. Chin. Med. Materia. Medica) 2012, 14, 2126(in Chinese).
21. [21]
  Yonekura-Sakakibara, K.; Tohge, T.; Niida, R.; Saito, K. J. Biol. Chem. 2007, 282, 14932.
22. [22]
  Luzhetskyy, A.; Méndez, C.; Salas, J. A.; Bechthold, A. Curr. Top. Med. Chem. 2008, 8, 680. doi: 10.2174/156802608784221514
23. [23]
  Yang, J.; Hoffmeister, D.; Liu, L.; Fu, X.; Thorson, J. S. Bioorg. Med. Chem. 2004, 12, 1577.
24. [24]
  Kren, V.; Martínková, L. Curr. Med. Chem. 2001, 8, 1303. doi: 10.2174/0929867013372193
25. [25]
  Jones, P.; Messner, B.; Nakajima, J.; Schäffner, A. R.; Saito, K. J. Biol. Chem. 2003, 278, 43910.
26. [26]
  Rojas Rodas, F.; Rodriguez, T. O.; Murai, Y.; Iwashina, T.; Sugawara, S.; Suzuki, M.; Nakabayashi, R.; Yonekura-Sakakibara, K.; Saito, K.; Kitajima, J.; Toda, K.; Takahashi, R. Plant Mol. Biol. 2014, 84, 287.
27. [27]
  McMullen, M. D.; Kross, H.; Snook, M. E.; Cortés-Cruz, M.; Houchins, K. E.; Musket, T. A.; Coe, E. H. Jr. J. Hered. 2004, 95, 225. doi: 10.1093/jhered/esh042
28. [28]
  Casas, M. I.; Falcone-Ferreyra, M. L.; Jiang, N.; Mejía-Guerra, M. K.; Rodríguez, E.; Wilson, T.; Engelmeier, J.; Casati, P.; Grotewold, E. Plant Cell 2016, 28, 1297. doi: 10.1105/tpc.16.00003
29. [29]
  Feng, K.; Chen, R.; Xie, K.; Chen, D.; Guo, B.; Liu, X.; Liu, J.; Zhang, M.; Dai, J. Org. Biomol. Chem. 2018, 16, 452. doi: 10.1039/C7OB02763J
30. [30]
  Frydman, A.; Weisshaus, O.; Bar-Peled, M.; Huhman, D. V.; Sumner, L. W.; Marin, F. R.; Lewinsohn, E.; Fluhr, R.; Gressel, J.; Eyal, Y. Plant J. 2004, 40, 88.
31. [31]
  Bar-Peled, M.; Lewinsohn, E.; Fluhr, R.; Gressel, J. J. Biol. Chem. 1991, 266, 20953.
32. [32]
  Frydman, A.; Liberman, R.; Huhman, D. V.; Carmeli-Weissberg, M.; Sapir-Mir, M.; Ophir, R.; Sumner, L.; Eyal, Y. Plant J. 2013, 73, 166.
33. [33]
  Liu, X. G.; Lin, C.; Ma, X. D.; Tan, Y.; Wang, J. Z.; Zeng, M. Front. Plant Sci. 2018, 9, 166.
34. [34]
  Welch, C. R.; Wu, Q.; Simon, J. E. Curr. Anal. Chem. 2008, 4, 75.
35. [35]
  Brugliera, F.; Holton, T. A.; Stevenson, T. W.; Farcy, E.; Lu, C. Y.; Cornish, E. C. Plant J. 1994, 5, 81. doi: 10.1046/j.1365-313X.1994.5010081.x
36. [36]
  Li, X. J.; Lai, B.; Zhao, J. T.; Qin, Y. H.; He, J. M.; Huang, X. M.; Wang, H.C.; Hu, G. B. Mol. Breed. 2016, 36, 93. doi: 10.1007/s11032-016-0518-3
37. [37]
  Li, P.; Li, Y. J.; Zhang, F. J.; Zhang, G. Z.; Jiang, X. Y.; Yu, H. M.; Hou, B. K. Plant J. 2017, 89, 85. doi: 10.1111/tpj.2017.89.issue-1
38. [38]
  Hsu, Y. H.; Tagami, T.; Matsunaga, K.; Okuyama, M.; Suzuki, T.; Noda, N.; Suzuki, M.; Shimura, H. Plant J. 2017, 89, 325. doi: 10.1111/tpj.13387
39. [39]
  McCue, K. F.; Allen, P. V.; Shepherd, L. V.; Blake, A.; Maccree, M. M.; Rockhold, D. R.; Novy, R. G.; Stewart, D.; Davies, H. V.; Belknap, W. R. Phytochemistry 2007, 68, 327.
40. [40]
  Uehara, Y.; Tamura, S.; Maki, Y.; Yagyu, K.; Mizoguchi, T.; Tamiaki, H.; Imai, T.; Ishii, T.; Ohashi, T.; Fujiyama, K.; Ishimizu, T. Biochem. Biophys. Res. Commun. 2017, 486, 130. doi: 10.1016/j.bbrc.2017.03.012
41. [41]
  Luzhetskyy, A.; Mayer, A.; Hoffmann, J.; Pelzer, S.; Holzenkämper, M.; Schmitt, B.; Wohlert, S. E.; Vente, A.; Bechthold, A. ChemBio-Chem 2007, 8, 599. doi: 10.1002/(ISSN)1439-7633
42. [42]
  Minotti, G.; Menna, P.; Salvatorelli, E.; Cairo, G.; Gianni, L. Pharmacol. Rev. 2004, 56, 185.
43. [43]
  Sianidis, G.; Wohlert, S. E.; Pozidis, C.; Karamanou, S.; Lu-zhetskyy, A.; Vente, A.; Economou, A. J. Biotechnol. 2006, 125, 425.
44. [44]
  Gullón, S.; Olano, C.; Abdelfattah, M. S.; Braña, A. F.; Rohr, J.; Méndez, C.; Salas, J. A. Appl. Environ. Microbiol. 2006, 72, 4172.
45. [45]
  Decker, H.; Rohr, J.; Motamedi, H.; Zähner, H.; Hutchinson, C. R. Gene 1995, 166, 121.
46. [46]
  Blanco, G.; Patallo, E. P.; Braña, A. F.; Trefzer, A.; Bechthold, A.; Rohr, J.; Méndez, C.; Salas, J. A. Chem. Biol. 2001, 8, 253. doi: 10.1016/S1074-5521(01)00010-2
47. [47]
  Doumith, M.; Legrand, R.; Lang, C.; Salas, J. A.; Raynal, M. C. Mol. Microbiol. 1999, 34, 1039.
48. [48]
  Zhang, Q. J. Chin. J. Clin. Rational Drug Use 2013, 6, 177(in Chinese).
49. [49]
  Zhang, C.; Griffith, B. R.; Fu, Q.; Albermann, C.; Fu, X.; Lee, I. K.; Li, L.; Thorson, J. S. Science 2006, 313, 1291. doi: 10.1126/science.1130028
50. [50]
  Chen, Y. L.; Chen, Y. H.; Lin, Y. C.; Tsai, K. C.; Chiu, H. T. J. Biol. Chem. 2009, 284, 7352.
51. [51]
  Ikeda, H.; Nonomiya, T.; Usami, M.; Ohta, T.; Omura, S. Proc. Natl. Acad. Sci. U. S. A. 1999, 96, 9509. doi: 10.1073/pnas.96.17.9509
52. [52]
  Ikeda, H.; Ishikawa, J.; Hanamoto, A.; Shinose, M.; Kikuchi, H.; Shiba, T. Nat. Biotechnol. 2003, 21, 526.
53. [53]
  Wu, Q.; Wu, J. B.; Li, Y. Chin. J. Antibiot. 1999, 24, 401.
54. [54]
  Wang, L. Y.; Li, S. T.; Li, Y. FEMS Microbiol. Lett. 2003, 220, 21. doi: 10.1016/S0378-1097(03)00044-2
55. [55]
  Li, X.; Wang, L.; Bai, L.; Yao, C.; Zhang, Y.; Zhang, R.; Li, Y. J. Appl. Microbiol. 2010, 108, 1544. doi: 10.1111/jam.2010.108.issue-5
56. [56]
  Wu, H.; Wang, W.; Han, S. Y. Microbiology (Beijing, China) 2007, 34, 148(in Chinese). doi: 10.3969/j.issn.0253-2654.2007.01.035
57. [57]
  Ochsner, U. A.; Fiechter, A.; Reiser, J. J. Biol. Chem. 1994, 269, 19787.
58. [58]
  Rahim, R.; Ochsner, U. A.; Olvera, C.; Graninger, M.; Messner, P.; Lam, J. S.; Soberón-Chávez, G. Mol. Microbiol. 2001, 40, 708.
59. [59]
  Lang, S.; Wullbrandt, D. Appl. Microbiol. Biotechnol. 1999, 51, 22.
60. [60]
  Grzegorzewicz, A. E.; Ma, Y.; Jones, V.; Crick, D.; Liav, A.; McNeil, M. R. Microbiology 2008, 154, 3724.
61. [61]
  Mills, J. A.; Motichka, K.; Jucker, M.; Wu, H. P.; Uhlik, B. C.; Stern, R. J.; Scherman, M. S.; Vissa, V. D.; Pan, F.; Kundu, M.; Ma, Y. F.; McNeil, M. J. Biol. Chem. 2004, 279, 43540.
62. [62]
  Harrus, D.; Kellokumpu, S.; Glumoff, T. Cell Mol. Life. Sci. 2018, 75, 833.
63. [63]
  Steiner, K.; Hagelueken, G.; Messner, P.; Schäffer, C.; Naismith, J. H. J. Mol. Biol. 2010, 397, 436. doi: 10.1016/j.jmb.2010.01.035
64. [64]
  Isiorho, E. A.; Liu, H. W.; Keatinge-Clay, A. T. Biochemistry 2012, 51, 1213.
65. [65]
  Waldron, C.; Matsushima, P.; Rosteck, P. R. Jr.; Broughton, M. C.; Turner, J.; Madduri, K.; Crawford, K. P.; Merlo, D. J.; Baltz, R. H. Chem. Biol. 2001, 8, 487.
66. [66]
  Zhao, Y.; Thorson, J. S. J. Org. Chem. 1998, 63, 7568. doi: 10.1021/jo981265n
67. [67]
  Sun, Q.; Li, X. J.; Sun, J.; Gong, S. S.; Liu, G.; Liu, G. D. Tetrahedron 2014, 70, 294. doi: 10.1016/j.tet.2013.11.059
68. [68]
  Marumo, K.; Lindqvist, L.; Verma, N.; Weintraub, A.; Reeves, P. R.; Lindberg, A. A. FEBS J. 1992, 204, 539.
69. [69]
  Schnaitman, C. A.; Klena, J. D. Microbiol. Rev. 1993, 57, 655.
70. [70]
  Stein, A.; Kula, M. R.; Elling, L. Glycoconjugate J. 1998, 15, 139. doi: 10.1023/A:1006912121278
71. [71]
  Graninger, M.; Nidetzky, B.; Heinrichs, D. E.; Whitfield, C.; Messner, P. J. Biol. Chem. 1999, 274, 25069.
72. [72]
  Usadel, B.; Kuschinsky, A. M.; Rosso, M. G.; Eckermann, N.; Pauly, M. Plant Physiol. 2004, 134, 286. doi: 10.1104/pp.103.034314
73. [73]
  Oka, T.; Nemoto, T.; Jigami, Y. J. Biol. Chem. 2007, 282, 5389. doi: 10.1074/jbc.M610196200
74. [74]
  Kim, B. G.; Jung, W. D.; Ahn, J. H. J. Plant Biol. 2013, 56, 7. doi: 10.1007/s12374-012-0333-2
75. [75]
  Yin, S.; Liu, M.; Kong, J. Q. Plant Physiol. Biochem. 2016, 109, 536. doi: 10.1016/j.plaphy.2016.10.029
76. [76]
  Martinez, V.; Ingwers, M.; Smith, J.; Glushka, J.; Yang, T.; Bar-Peled, M. J. Biol. Chem. 2012, 287, 879.
77. [77]
  Gantt, R. W.; Peltier-Pain, P.; Cournoyer, W. J.; Thorson, J. S. Nat. Chem. Biol. 2011, 7, 685. doi: 10.1038/nchembio.638
78. [78]
  Erijman, A.; Aizner, Y.; Shifman, J. M. Biochemistry. 2011, 50, 602.
79. [79]
  Franco, O. L. FEBS Lett. 2011, 585, 995.
80. [80]
  Mo, T.; Liu, X.; Liu, Y. Y.; Wang, X. H.; Zhang, L.; Wang, J.; Zhang, Z. X.; Shi, S. P.; Tu, P. F. RSC Adv. 2016, 6, 84616. doi: 10.1039/C6RA16251G
81. [81]
  Parajuli, P.; Pandey, R. P.; Trang, N. T. H.; Oh, T. J.; Sohng, J. K. Carbohydr. Res. 2015, 418, 13. doi: 10.1016/j.carres.2015.09.010
82. [82]
  Parajuli, P.; Pandey R. P.; Darsandhari, S.; Yong, I. P.; Sohng, J. K. J. Carbohydr. Chem. 2016, 35, 367.
83. [83]
  Ohashi, T.; Hasegawa, Y.; Misaki, R.; Fujiyama, K. Appl. Microbiol. Biotechnol. 2016, 100, 687.
84. [84]
  Pandey, R. P.; Parajuli, P.; Gurung, R. B.; Sohng, J. K. Enzyme Microb. Tech. 2016, 91, 26.
85. [85]
  Yoshikuni, Y.; Ferrin, T. E.; Keasling, J. D. Nature 2006, 440, 1078.
86. [86]
  Kim, B. G.; Kim, H. J.; Ahn, J. H. J. Agric. Food Chem. 2012, 60, 11143. doi: 10.1021/jf302123c
87. [87]
  Yang, S. M.; Han, S. H.; Kim, B. G.; Ahn, J. H. J. Ind. Microbiol. Biotechnol. 2014, 41, 1311.
88. [88]
  Roepke, J.; Bozzo, G. G. ChemBioChem 2013, 14, 2418. doi: 10.1002/cbic.v14.18
89. [89]
  Kim, H. J.; Kim, B. G.; Ahn, J. H. Appl. Microbiol. Biotechnol. 2013, 97, 5275.
90. [90]
  Thuan, N. H.; Malla, S.; Trung, N. T.; Dhakal, D.; Pokhrel, A. R.; Chu, L. L.; Sohng, J. K. World J. Microbiol. Biotechnol. 2017, 33, 36. doi: 10.1007/s11274-017-2208-7
91. [91]
  Parajuli, P.; Pandey, R. P.; Trang, N. T.; Chaudhary, A. K.; Sohng, J. K. Microb. Cell Fact. 2015, 14, 76.
92. [92]
  Frydman, A. Weisshaus, O.; Huhman, D. V.; Sumner, L. W.; Bar-Peled, M.; Lewinsohn, E.; Fluhr, R.; Gressel, J.; Eyal, Y. J. Agric. Food Chem. 2005, 53, 9708.
93. [93]
  Gong, Z. J.; Peng, Y. F.; Zhang, Y. T.; Song, G. T.; Chen, W. J. Jia, S. R.; Wang, Q. H. Chin. J. Biotechnol. 2015, 31, 1050(in Chinese)
94. [94]
  Du, J.; Zhang, A.; Hao, J.; Wang, J. Biotechnol. Lett. 2017, 39, 1041.
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沈阳化工大学材料科学与工程学院沈阳 110142