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PMID: 3780721 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Energy dependence of protein translocation into chloroplasts.

European journal of biochemistry ·Vol. 160 ·No. 3 ·1986-11-03 ·Pages 563-70

Flügge UI, Hinz G

Abstract

The translocation of in vitro synthesized precursor proteins into intact spinach chloroplasts was investigated with respect to its energy requirement. It was demonstrated that MgATP itself, and not a transmembrane electrochemical gradient across the envelope membrane, promotes protein import. By manipulating the external and the stromal level of MgATP, we provided evidence that MgATP energized the protein import not within the chloroplast but at the outside of the envelope membrane. It is postulated that an MgATP-dependent phosphorylation/dephosphorylation cycle at the outer membrane face was involved in the course of protein translocation into the chloroplast.

MeSH Terms
Adenosine Triphosphate/metabolism Carbonyl Cyanide m-Chlorophenyl Hydrazone/pharmacology Cations, Divalent Chloroplasts/drug effects,metabolism Darkness Energy Metabolism Kinetics Light Methionine/metabolism Plant Proteins/biosynthesis,metabolism Plants/metabolism
Chemicals
Cations, Divalent Plant Proteins Carbonyl Cyanide m-Chlorophenyl Hydrazone Adenosine Triphosphate Methionine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Flügge U I
Hinz G
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1986-11-03
Pages
563-70
Language
English
Region
England
NLM ID
0107600
Subset
IM
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