Literature DB >> 15247383

Novel biosynthetic pathway of castasterone from cholesterol in tomato.

Tae-Wuk Kim1, Soo Chul Chang, June Seung Lee, Suguru Takatsuto, Takao Yokota, Seong-Ki Kim.   

Abstract

Endogenous brassinosteroids (BRs) in tomato (Lycopersicon esculentum) seedlings are known to be composed of C27- and C28-BRs. The biosynthetic pathways of C27-BRs were examined using a cell-free enzyme solution prepared from tomato seedlings that yielded the biosynthetic sequences cholesterol --> cholestanol and 6-deoxo-28-norteasterone <--> 6-deoxo-28-nor-3-dehydroteasterone <--> 6-deoxo-28-nortyphasterol --> 6-deoxo-28-norcastasterone --> 28-norcastasterone (28-norCS). Arabidopsis CYP85A1 that was heterologously expressed in yeast mediated the conversion of 6-deoxo-28-norCS to 28-norCS. The same reaction was catalyzed by an enzyme solution from wild-type tomato but not by an extract derived from a tomato dwarf mutant with a defect in CYP85. Furthermore, exogenously applied 28-norCS restored the abnormal growth of the dwarf mutant. These findings indicate that the C-6 oxidation of 6-deoxo-28-norCS to 28-norCS in tomato seedlings is catalyzed by CYP85, just as in the conversion of 6-deoxoCS to CS. Additionally, the cell-free solution also catalyzed the C-24 methylation of 28-norCS to CS in the presence of NADPH and S-adenosylmethionine (SAM), a reaction that was clearly retarded in the absence of NADPH and SAM. Thus it seems that C27-BRs, in addition to C28-BRs, are important in the production of more active C28-BRs and CS, where a SAM-dependent sterol methyltransferase appears to biosynthetically connect C27-BRs to C28-BRs. Moreover, the tomato cell-free solution converted CS to 26-norCS and [2H6]CS to [2H3]28-norCS, suggesting that C-28 demethylation is an artifact due to an isotope effect. Although previous feeding experiments employing [2H6]CS suggested that 28-norCS was synthesized from CS in certain plant species, this is not supported in planta. Altogether, this study demonstrated for the first time, to our knowledge, that 28-norCS is not synthesized from CS but from cholesterol. In addition, CS and [2H6]CS were not converted into BL and [2H6]BL, respectively, confirming an earlier finding that the active BR in tomato seedlings is not BL but CS. In conclusion, the biosynthesis of 28-norBRs appears to play a physiologically important role in maintaining homeostatic levels of CS in tomato seedlings.

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Year:  2004        PMID: 15247383      PMCID: PMC519043          DOI: 10.1104/pp.104.043588

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  41 in total

1.  A putative role for the tomato genes DUMPY and CURL-3 in brassinosteroid biosynthesis and response.

Authors:  C V Koka; R E Cerny; R G Gardner; T Noguchi; S Fujioka; S Takatsuto; S Yoshida; S D Clouse
Journal:  Plant Physiol       Date:  2000-01       Impact factor: 8.340

2.  Improved method for high efficiency transformation of intact yeast cells.

Authors:  D Gietz; A St Jean; R A Woods; R H Schiestl
Journal:  Nucleic Acids Res       Date:  1992-03-25       Impact factor: 16.971

3.  Arabidopsis det2 is defective in the conversion of (24R)-24-methylcholest-4-En-3-one to (24R)-24-methyl-5alpha-cholestan-3-one in brassinosteroid biosynthesis.

Authors:  T Noguchi; S Fujioka; S Takatsuto; A Sakurai; S Yoshida; J Li; J Chory
Journal:  Plant Physiol       Date:  1999-07       Impact factor: 8.340

4.  The ratio of campesterol to sitosterol that modulates growth in Arabidopsis is controlled by STEROL METHYLTRANSFERASE 2;1.

Authors:  A Schaeffer; R Bronner; P Benveniste; H Schaller
Journal:  Plant J       Date:  2001-03       Impact factor: 6.417

5.  Cloning, yeast expression, and characterization of the coupling of two distantly related Arabidopsis thaliana NADPH-cytochrome P450 reductases with P450 CYP73A5.

Authors:  P Urban; C Mignotte; M Kazmaier; F Delorme; D Pompon
Journal:  J Biol Chem       Date:  1997-08-01       Impact factor: 5.157

6.  Brassinolide and [26, 28-2H6]brassinolide are differently demethylated by loss of C-26 and C-28, respectively, in Marchantia polymorpha.

Authors:  T W Kim; S C Chang; J Choo; T Watanabe; S Takatsuto; T Yokota; J S Lee; S Y Kim; S K Kim
Journal:  Plant Cell Physiol       Date:  2000-10       Impact factor: 4.927

7.  The LKA gene is a BRASSINOSTEROID INSENSITIVE 1 homolog of pea.

Authors:  Takahito Nomura; Gerard J Bishop; Tsuyoshi Kaneta; James B Reid; Joanne Chory; Takao Yokota
Journal:  Plant J       Date:  2003-11       Impact factor: 6.417

8.  A rice brassinosteroid-deficient mutant, ebisu dwarf (d2), is caused by a loss of function of a new member of cytochrome P450.

Authors:  Zhi Hong; Miyako Ueguchi-Tanaka; Kazuto Umemura; Sakurako Uozu; Shozo Fujioka; Suguru Takatsuto; Shigeo Yoshida; Motoyuki Ashikari; Hidemi Kitano; Makoto Matsuoka
Journal:  Plant Cell       Date:  2003-11-13       Impact factor: 11.277

9.  A dwarf mutant strain of Pharbitis nil, Uzukobito (kobito), has defective brassinosteroid biosynthesis.

Authors:  Yoshihito Suzuki; Kazuyuki Saso; Shozo Fujioka; Shigeo Yoshida; Eiji Nitasaka; Shinji Nagata; Hiromichi Nagasawa; Suguru Takatsuto; Isomaro Yamaguchi
Journal:  Plant J       Date:  2003-11       Impact factor: 6.417

10.  BRI1/BAK1, a receptor kinase pair mediating brassinosteroid signaling.

Authors:  Kyoung Hee Nam; Jianming Li
Journal:  Cell       Date:  2002-07-26       Impact factor: 41.582

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  7 in total

1.  Arabidopsis CYP85A2, a cytochrome P450, mediates the Baeyer-Villiger oxidation of castasterone to brassinolide in brassinosteroid biosynthesis.

Authors:  Tae-Wuk Kim; Jung-Yun Hwang; Young-Soo Kim; Se-Hwan Joo; Soo Chul Chang; June Seung Lee; Suguru Takatsuto; Seong-Ki Kim
Journal:  Plant Cell       Date:  2005-07-15       Impact factor: 11.277

Review 2.  Isoprenoid-derived plant signaling molecules: biosynthesis and biological importance.

Authors:  Danuše Tarkowská; Miroslav Strnad
Journal:  Planta       Date:  2018-03-12       Impact factor: 4.116

3.  Biosynthesis of a cholesterol-derived brassinosteroid, 28-norcastasterone, in Arabidopsis thaliana.

Authors:  Se-Hwan Joo; Tae-Wuk Kim; Seung-Hyun Son; Woo Sung Lee; Takao Yokota; Seong-Ki Kim
Journal:  J Exp Bot       Date:  2011-12-13       Impact factor: 6.992

4.  Drought-tolerant and drought-sensitive genotypes of maize (Zea mays L.) differ in contents of endogenous brassinosteroids and their drought-induced changes.

Authors:  Lenka Tůmová; Danuše Tarkowská; Kateřina Řehořová; Hana Marková; Marie Kočová; Olga Rothová; Petr Čečetka; Dana Holá
Journal:  PLoS One       Date:  2018-05-24       Impact factor: 3.240

5.  Function and molecular regulation of DWARF1 as a C-24 reductase in brassinosteroid biosynthesis in Arabidopsis.

Authors:  Ji Hyun Youn; Tae-Woo Kim; Se-Hwan Joo; Seung-Hyun Son; Jeehee Roh; Sunyoung Kim; Tae-Wuk Kim; Seong-Ki Kim
Journal:  J Exp Bot       Date:  2018-04-09       Impact factor: 6.992

6.  Seed-Specific Expression of Arabidopsis AtCYP85A2 Produces Biologically Active Brassinosteroids Such as Castasterone and Brassinolide to Improve Grain Yield and Quality in Seeds of Brachypodium Distachyon.

Authors:  Jeehee Roh; Jinyoung Moon; Ye Eun Lee; Chan Ho Park; Seong-Ki Kim
Journal:  Front Plant Sci       Date:  2021-04-01       Impact factor: 5.753

7.  Gene regulation network analyses of pistil development in papaya.

Authors:  Zhenyang Liao; Fei Dong; Juan Liu; Lele Xu; Amy Marshall-Colon; Ray Ming
Journal:  BMC Genomics       Date:  2022-01-05       Impact factor: 3.969

  7 in total

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