Literature DB >> 12226251

N4-Hexanoylspermidine, a New Polyamine-Related Compound That Accumulates during Ovary and Petal Senescence in Pea.

M. A. Perez-Amador1, J. Carbonell, J. L. Navarro, T. Moritz, M. H. Beale, M. J. Lewis, P. Hedden.   

Abstract

A previously unknown polyamine conjugate that accumulates in senescing ovaries of pea (Pisum sativum L.) was shown by mass spectrometry, nuclear magnetic resonance, and chemical synthesis to be N4-hexanoylspermidine (hexanoyl-spd) This structure was indicated by analysis of the dansylated polyamine using fast atom bombardment mass spectrometry, following purification by high-performance liquid chromatography. Furthermore, acid hydrolysis of the compound yielded spermidine and hexanoic acid. 1H-nuclear magnetic resonance suggested that spermidine was substituted at N4 in the conjugate. Hexanoyl-spd was synthesized, and its didansyl derivative was shown to have an identical mass spectrum and high-performance liquid chromatography retention time as the derivatized natural compound. Further confirmation of its structure was obtained by comparison of the synthetic and natural polyamines as trifluoroacetyl derivatives using gas chromatography-mass spectrometry. This new polyamine conjugate is present in pea ovaries at low levels at anthesis and its concentration remains low in developing seeded fruit or in parthenocarpic fruit that have been induced by application of growth regulators to emasculated flowers or by topping the plant. Conjugate levels are also low in parthenocarpic fruit induced naturally in the slender (la crys) mutant. However, levels of hexanoyl-spd increase progressively in senescing petals and ovaries, beginning at anthesis or 2 d later, respectively.

Entities:  

Year:  1996        PMID: 12226251      PMCID: PMC160904          DOI: 10.1104/pp.110.4.1177

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


  6 in total

1.  Electron capture gas-liquid chromatography of short chain acids as their 2,2,2-trichloroethyl esters.

Authors:  C C Alley; J B Brooks; G Choudhary
Journal:  Anal Chem       Date:  1976-02       Impact factor: 6.986

Review 2.  Functions of polyamine acetylation.

Authors:  N Seiler
Journal:  Can J Physiol Pharmacol       Date:  1987-10       Impact factor: 2.273

3.  Polyamines and Flower Development in the Male Sterile Stamenless-2 Mutant of Tomato (Lycopersicon esculentum Mill.) : I. Level of Polyamines and Their Biosynthesis in Normal and Mutant Flowers.

Authors:  R Rastogi; V K Sawhney
Journal:  Plant Physiol       Date:  1990-06       Impact factor: 8.340

Review 4.  Polyamines in plant physiology.

Authors:  A W Galston; R K Sawhney
Journal:  Plant Physiol       Date:  1990-10       Impact factor: 8.340

5.  Arginine Decarboxylase and Putrescine Oxidase in Ovaries of Pisum sativum L. (Changes during Ovary Senescence and Early Stages of Fruit Development).

Authors:  M. A. Perez-Amador; J. Carbonell
Journal:  Plant Physiol       Date:  1995-03       Impact factor: 8.340

6.  Tumor inhibitors. 43. Solapalmitine and solapalmitenine, two novel alkaloid tumor inhibitors from Solanum tripartitium.

Authors:  S M Kupchan; A P Davies; S J Barboutis; H K Schnoes; A L Burlingame
Journal:  J Org Chem       Date:  1969-12       Impact factor: 4.354

  6 in total
  1 in total

1.  Arginase, Arginine Decarboxylase, Ornithine Decarboxylase, and Polyamines in Tomato Ovaries (Changes in Unpollinated Ovaries and Parthenocarpic Fruits Induced by Auxin or Gibberellin).

Authors:  D. Alabadi; M. S. Aguero; M. A. Perez-Amador; J. Carbonell
Journal:  Plant Physiol       Date:  1996-11       Impact factor: 8.340

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.