Literature DB >> 16663261

Cell Walls of Phaseolus vulgaris Leaves Contain the Azocoll-Digesting Proteinase.

W van der Wilden1, J H Segers, M J Chrispeels.   

Abstract

The leaves of Phaseolus vulgaris L. cv Greensleeves contain an endopeptidase with a pH optimum of 9.0 and an isoelectric point between 10.0 and 10.5. This endopeptidase is the only abundant Azocoll-digesting proteinase in the leaves. The activity of this enzyme is highest in immature leaves and declines as the leaf matures and senesces. Enzymically isolated protoplasts contain very little of this proteinase. The proteinase can be recovered readily from the extracellular fluid obtained by gentle centrifugation of leaf strips vacuum-infiltrated with a buffered solution. These experiments indicate that the Azocoll digesting proteinase is located in the periplasmic space and/or the cell wall.

Entities:  

Year:  1983        PMID: 16663261      PMCID: PMC1066509          DOI: 10.1104/pp.73.3.576

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


  4 in total

1.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

2.  Purification and characterization of vicilin peptidohydrolase, the major endopeptidase in the cotyledons of mung-bean seedlings.

Authors:  B Baumgartner; M J Chrispeels
Journal:  Eur J Biochem       Date:  1977-07-15

3.  Hemoglobin-digesting Acid Proteinases in Soybean Leaves: CHARACTERISTICS AND CHANGES DURING LEAF MATURATION AND SENESCENCE.

Authors:  L V Ragster; M J Chrispeels
Journal:  Plant Physiol       Date:  1981-01       Impact factor: 8.340

4.  Azocoll-digesting Proteinases in Soybean Leaves: Characteristics and Changes during Leaf Maturation and Senescence.

Authors:  L V Ragster; M J Chrispeels
Journal:  Plant Physiol       Date:  1979-11       Impact factor: 8.340

  4 in total
  11 in total

1.  Purification and Developmental Analysis of a Metalloendoproteinase from the Leaves of Glycine max.

Authors:  J S Graham; J Xiong; J W Gillikin
Journal:  Plant Physiol       Date:  1991-10       Impact factor: 8.340

2.  Degradation of tobacco pathogenesis-related proteins : evidence for conserved mechanisms of degradation of pathogenesis-related proteins in plants.

Authors:  I Rodrigo; P Vera; L C Van Loon; V Conejero
Journal:  Plant Physiol       Date:  1991-02       Impact factor: 8.340

3.  Proteins in intercellular washing fluid from noninoculated and rust-affected leaves of wheat and barley.

Authors:  D W Holden; R Rohringer
Journal:  Plant Physiol       Date:  1985-08       Impact factor: 8.340

4.  Subcellular Localization of Proteases in Developing Leaves of Oats (Avena sativa L.).

Authors:  H C van der Valk; L C van Loon
Journal:  Plant Physiol       Date:  1988-06       Impact factor: 8.340

5.  Apparent Inhibition of beta-Fructosidase Secretion by Tunicamycin May Be Explained by Breakdown of the Unglycosylated Protein during Secretion.

Authors:  L Faye; M J Chrispeels
Journal:  Plant Physiol       Date:  1989-03       Impact factor: 8.340

6.  Pathogenesis-related proteins of tomato : p-69 as an alkaline endoproteinase.

Authors:  P Vera; V Conejero
Journal:  Plant Physiol       Date:  1988-05       Impact factor: 8.340

7.  Proteolytic processing of class IV chitinase in the compatible interaction of bean roots with Fusarium solani.

Authors:  J Lange; U Mohr; A Wiemken; T Boller; R Vögeli-Lange
Journal:  Plant Physiol       Date:  1996-08       Impact factor: 8.340

8.  Differential expression profiles of growth-related genes in the elongation zone of maize primary roots.

Authors:  Michal Bassani; Peter M Neumann; Shimon Gepstein
Journal:  Plant Mol Biol       Date:  2004-10       Impact factor: 4.076

9.  Purification and Developmental Analysis of an Extracellular Proteinase from Young Leaves of Soybean.

Authors:  J. Huangpu; J. S. Graham
Journal:  Plant Physiol       Date:  1995-07       Impact factor: 8.340

10.  Nucellain, a barley homolog of the dicot vacuolar-processing protease, is localized in nucellar cell walls.

Authors:  C Linnestad; D N Doan; R C Brown; B E Lemmon; D J Meyer; R Jung; O A Olsen
Journal:  Plant Physiol       Date:  1998-12       Impact factor: 8.340

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