Identification and characterization of an Ipomoea nil glucosyltransferase which metabolizes some phytohormones

Biochemical and Biophysical Research Communications

Volumn 361, Issue 4, 2007, Pages 980-986

  Suzuki, Hiroyuki ^a   Hayase, Hiroki ^a   Nakayama, Akira ^b   Yamaguchi, Isomaro ^b   Asami, Tadao ^a   Nakajima, Masatoshi ^a  

^a UNIVERSITY OF TOKYO   (Japan)

^b MAEBASHI INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

Glucosyltransferase; Glycosylation; Ipomoea nil; Metabolism; Phytohormone

Indexed keywords

2 TRANS ABSCISIC ACID; ABSCISIC ACID; CARBON 14; CARBOXYL GROUP; GLUCOSYLTRANSFERASE; INDOLEACETIC ACID; INGTASE1; JASMONIC ACID; PHYTOHORMONE; SALICYLIC ACID; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; ENZYME ACTIVITY; GAS CHROMATOGRAPHY; IPOMOEA NIL; MASS SPECTROMETRY; NONHUMAN; POLARIZATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; THIN LAYER CHROMATOGRAPHY;

BASE SEQUENCE; CLONING, MOLECULAR; GLUCOSYLTRANSFERASES; IPOMOEA NIL; MOLECULAR SEQUENCE DATA; PLANT GROWTH REGULATORS; PLANT PROTEINS; SEQUENCE ALIGNMENT; SUBSTRATE SPECIFICITY; URIDINE DIPHOSPHATE GLUCOSE;

IPOMOEA; IPOMOEA NIL;

EID: 34547882437     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.07.147     Document Type: Article

References (36)

1. Weymouth-Wilson A.C. The role of carbohydrates in biologically active natural products. Nat. Prod. Rep. 14 (1997) 99-110
2. Koeller K.M., and Wong C.H. Complex carbohydrate synthesis tools for glycobiologists: enzyme-based approach and programmable one-pot strategies. Glycobiology 10 (2000) 1157-1169
3. Harborne J.B., and Baxter H. Flavone O-glycosides, flavonol O-glycosides and C-glycosylflavones,;;. In: Harborne J.B., and Baxter H. (Eds). The Handbook of Natural Flavonoids vol. 1 (1999), John Wiley & Sons Inc, Chichester, UK 297-549
4. Chen X., Zhu Q., and Jia Z. Pregnane glycoside, lignan glycosides, triterpene glycosyl ester and flavonoid glycosides from Rubus amabilis. Planta. Med. 67 (2001) 270-273
5. Miyakoshi M., Ida Y., Isoda S., and Shoji J. 3 alpha-hydroxy-oleanane-type triterpene glycosyl esters from leaves of Acanthopanax spinosus. Phytochemistry 34 (1993) 1599-1602
6. Kazamierz K., and Jeff S. Phytohormone conjugates: nature and function. Crit. Rev. Plant Sci. 14 (1995) 283-298
7. Lehmann H., and Schuette H.R. Purification and characterization of an abscisic acid glycosylating enzyme from cell suspension cultures of Macleaya microcarpa. Z. Pflanzenphysiology 96 (1980) 277-280
8. Bray E.A., and Zeevaart J.A.D. The compartmentation of abscisic acid and beta-d-glucopyranosyl abscisate in mesophyll cells. Plant Physiol. 79 (1985) 719-722
9. Lehmann H., and Glund K. Abscisic acid metabolism: vacuolar/extravacuolar distribution of metabolites. Planta 168 (1986) 559-562
10. Milborrow B.V. The stability of conjugated abscisic acid during wilting. J. Exp. Bot. 29 (1978) 1059-1066
11. Johnson J.D., and Ferrell W.K. The relationship of abscisic acid metabolism to stomatal conductance in douglas fir during water stress. Physiol. Plant 55 (1982) 431-437
12. Cohen J.D., and Bandurski R.S. The bound auxins: protection of indole-3-acetic acid from peroxidase catalysed oxidation. Planta 139 (1978) 203-208
13. Cohen J.D., and Bandurski R.S. Chemistry and physiology of the bound auxins. Annu. Rev. Plant Physiol. 33 (1982) 403-730
14. Yokota T., Murofushi N., Takahashi N., and Tamura S. Gibberellins in immature seeds of Pharbitis nil Part III. Isolation and structure of gibberellin glucosides. Agric. Biol. Chem. 35 (1971) 573-582
15. Rood S.B., Pharis R.P., and Koshioka M. Reversible conjugation of gibberellin in situ in maize. Plant Physiol. 73 (1983) 340-346
16. Letham D.S., and Palni L.M.S. The biosynthesis and metabolism of cytokinins. Annu. Rev. Plant Physiol. 34 (1983) 163-197
17. Jones R.J., and Schreiber B.M.N. Role and function of cytokinin oxidase in plants. Plant Growth Regul. 23 (1997) 123-134
18. Brzobohaty B., Moore I., Kristoffersen P., Bako L., Campos N., Schell J., and Palme K. Release of active cytokinin by a β glucosidase localized to the maize root meristem. Science 262 (1993) 1051-1054
19. Fujioka S., and Yokota T. Biosynthesis and metabolism of brassinosteroids. Annu. Rev. Plant Biol. 54 (2003) 137-164
20. Campbell J.A., Davies G.J., Bulone V., and Henrissat B. A classification of nucleotide-diphospho-sugar glycosyltransferases based on amino acid sequence similarities. Biochem. J. 326 (1997) 929-939
21. Szerszen J.B., Szczyglowski K., and Bandurski R.S. iaglu, a gene from Zea mays involved in conjugation of growth hormone indole-3-acetic acid. Science 265 (1994) 1699-1701
22. Jackson R.G., Lim E.K., Li Y., Kowalczyk M., Sandberg G., Hoggett J., Ashford D.A., and Bowles D.J. Identification and biochemical characterization of an Arabidopsis indole-3-acetic acid glucosyltransferases. J. Biol. Chem. 276 (2001) 4350-4356
23. Xu Z.J., Nakajima M., Suzuki Y., and Yamaguchi I. Cloning and characterization of the abscisic acid-specific glucosyltransferase gene from adzuki bean seedlings. Plant Physiol. 129 (2002) 1285-1295
24. Priest D.M., Jackson R.G., Ashford D.A., Abrams S.R., and Bowles D.J. The use of abscisic acid analogues to analyse the substrate selectivity of UGT71B6, a UDP-glycosyltransferase of Arabidopsis thaliana. FEBS Lett. 579 (2005) 4454-4458
25. Martin R.C., Mok M.C., and Mok D.W.S. Isolation of a cytokinin gene, ZOG1, encoding zeatin O-glucosyltransferase from Phaseolus lunatus. Proc. Natl. Acad. Sci. USA 96 (1999) 284-289
26. Martin R.C., Mok M.C., Habben J.E., and Mok D.W.S. A maize cytokinin gene encoding an O-glucosyltransferase specific to cis-zeatin. Proc. Natl. Acad. Sci. USA 98 (2001) 5922-5926
27. Hou B., Lim E.K., Higgins G.S., and Bowles D.J. N-glucosylation of cytokinin by glycosyltransferases of Arabidopsis thaliana. J. Biol. Chem. 279 (2004) 47822-47832
28. Poppenberger B., Fujioka S., Soeno K., George G.L., Vaistij F.E., Hiranuma S., Seto H., Takatsuto S., Adam G., Yoshida S., and Bowles D.J. The UGT73C5 of Arabidopsis thaliana glucosylates brassinosteroids. Proc. Natl. Acad. Sci. USA 102 (2005) 15253-15258
29. Logemann J., Schell J., and Willmitzer L. Improved method for the isolation of RNA from plant tissues. Anal. Biochem. 163 (1982) 16-20
30. Ross J., Li Y., Lim E.K., and Bowles D.J. Higher plant glycosyltransferases. Genome Biol. 2 (2001) 3004.1-3004.6
31. Laurence F.T., Baltz R., Chong J., Kauffmann S., Fritig B., and Saindrenan P. Two tobacco genes induced by infection, elicitor and salicylic acid encode glucosyltransferases acting on phenylpropanoids and benzoic acid derivatives, including salicylic acid. FEBS Lett. 437 (1998) 319-323
32. Hui S., Xianzhi H., Lahoucine A., Jack W.B., Richard A.D., and Xiaoqiang W. Crystal structures of a multifunctional triterpene/flavonoid glycosyltransferase from Medicago truncatula. Plant Cell 17 (2005) 3141-3154
33. Kubo A., Arai Y., Nagashima S., and Yoshikawa T. Alteration of sugar donor specificities of plant glycosyltransferases by a single point mutation. Arch. Biochem. Biophys. 429 (2004) 198-203
34. Schmidt J., and Schneider G. Capillary gas chromatography/mass spectrometry of permethylated gibberellin glucosides. Biomed. Environ. Mass Spectrom. 17 (1988) 7-13
35. Coleman J.O.D., BlakeKalff M.M.A., and Davies T.G.E. Detoxification of xenobiotics by plants: chemical modification and vacuolar compartmentation. Trends Plant Sci. 2 (1997) 144-151
36. Pedras M.S.C., Zaharia I.L., Gai Y., Zhou Y., and Ward D.E. In planta sequential hydroxylation and glycosylation of a fungal phytotoxin: avoiding cell death and overcoming the fungal invader. Proc. Natl. Acad. Sci. USA 98 (2001) 747-752