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Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins

Purified chloroplasts from spinach and pea leaves were subfractionated into envelope, thylakoid, and stroma fractions and were analyzed for calmodulin-binding proteins using a 125I-calmodulin gel overlay assay. Calmodulin binding was primarily associated with a major polypeptide (Mr 33,000) in the e...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1983
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112670/
https://www.ncbi.nlm.nih.gov/pubmed/6313700
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collection PubMed
description Purified chloroplasts from spinach and pea leaves were subfractionated into envelope, thylakoid, and stroma fractions and were analyzed for calmodulin-binding proteins using a 125I-calmodulin gel overlay assay. Calmodulin binding was primarily associated with a major polypeptide (Mr 33,000) in the envelope membrane fraction. In contrast, major calmodulin-binding proteins were not detected in the thylakoid or stroma fractions. Our results provide the first evidence of calmodulin- binding proteins in the chloroplast envelope, and raise the possibility that calmodulin may contribute to the regulation of chloroplast function through its interaction with calmodulin-binding proteins in the chloroplast envelope. In addition, our results combined with those of other investigators support the proposal that subcellular organelles may be a primary site of calmodulin action.
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spelling pubmed-21126702008-05-01 Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins J Cell Biol Articles Purified chloroplasts from spinach and pea leaves were subfractionated into envelope, thylakoid, and stroma fractions and were analyzed for calmodulin-binding proteins using a 125I-calmodulin gel overlay assay. Calmodulin binding was primarily associated with a major polypeptide (Mr 33,000) in the envelope membrane fraction. In contrast, major calmodulin-binding proteins were not detected in the thylakoid or stroma fractions. Our results provide the first evidence of calmodulin- binding proteins in the chloroplast envelope, and raise the possibility that calmodulin may contribute to the regulation of chloroplast function through its interaction with calmodulin-binding proteins in the chloroplast envelope. In addition, our results combined with those of other investigators support the proposal that subcellular organelles may be a primary site of calmodulin action. The Rockefeller University Press 1983-11-01 /pmc/articles/PMC2112670/ /pubmed/6313700 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins
title Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins
title_full Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins
title_fullStr Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins
title_full_unstemmed Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins
title_short Analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins
title_sort analysis of suborganellar fractions from spinach and pea chloroplasts for calmodulin-binding proteins
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112670/
https://www.ncbi.nlm.nih.gov/pubmed/6313700