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Multiforn of γ-Glutamyltransfemse in Higher Plants and Cysteine Recycle

Research Project

Project/Area Number 14560052
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Plant nutrition/Soil science
Research InstitutionKyoto University

Principal Investigator

SEKIYA Jiro  KYOTO UNIVERSITY, Graduate School of Agriculture, Professor, 農学研究科, 教授 (10035123)

Co-Investigator(Kenkyū-buntansha) KOIZUMI Yukio  KYOTO UNIVERSITY, Graduate School of Agriculture, Instructor, 農学研究科, 助手 (40293914)
Project Period (FY) 2002 – 2003
Project Status Completed (Fiscal Year 2003)
Budget Amount *help
¥3,600,000 (Direct Cost: ¥3,600,000)
Fiscal Year 2003: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2002: ¥2,200,000 (Direct Cost: ¥2,200,000)
Keywordsγ-glutamyltransferase / mdish / bound γ-glutamyltransferase / soluble γ-glutamyltransferase / transgenic tobacco / multiform / glutathione catabolism / グルタミル基転移酵素 / 可溶性γ-GT / 細胞壁結合性γ-GT
Research Abstract

1 Occurrence of two forms of radish γ-glutamyltransferases (GGT; EC.2.3.2.2), soluble and cell wall bound ones, were demonstrated in many plants including radish (Raphanus sativus).
2 We cloned three cDNAs (rsggt1, AB098475; rsggt2, AB102676;rsggt3, unregistered) predicted to encode radish soluble GGTs, sequenced them and analyzed their properties. These cDNA seems to encode a heterodimeric type of GGTs homologous to mammalians GGTs.
3 These three genes were transcribed by organ and tissue specific manner: rsggt1 was expressed characteristically in immature seeds and cotyledons; rsggt2 in cotyledons, leaves and roots; and rsggt 3 in leaves, roots and immature seeds.
4 We transformed tobacco plants with rsggt1 and rsggt2. Transformed tobacco plants grew normally. They developed higher level of GGT activity, although wild type tobacco plants exhibited a very low GGT activity. Expressed GGT activity was found in the bound fraction, although cDNA used encoded soluble radish GGT. To understand this discrepancy remains to be solved in future.
5 We purified bound GGTs from radish cotyledons. The bound GGT was a monomeric enzyme unlike soluble GGTs. cDNA was presumed to be highly homologous to Arabidopsis cDNA (AK118068) encoding putative β-1,3-glucanase. Tobacco plants transformed with putative β-1,3-glucanase cDNA exhibited elevated level of GGT activity, but not β-1,3-glucanase.
6 We measured thiol compounds in apoplastic space of leaves of transgenic and wild type tobacco plants. Decreased level of glutathione (GSH) and elevated level of cysteinylglycine, a product of GGT reaction, were found in transgenic plants. These findings suggest that cell wall bound GGTs participate in GSH catabolism in apoplastic space.

Report

(3 results)
  • 2003 Annual Research Report   Final Research Report Summary
  • 2002 Annual Research Report

URL: 

Published: 2002-04-01   Modified: 2016-04-21  

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