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PMID: 5938657 Published · ppublish English Journal Article

Synthesis and possible character of a high-energy intermediate in bacterial photophosphorylation.

The Biochemical journal ·Vol. 98 ·No. 1 ·1966-01-00 ·Pages 321-9

Horio T, Nishikawa K, Yamashita J

Abstract

1. In photophosphorylation with chromatophores from Rhodospirillum rubrum, evidence is presented for the synthesis of activated precursors of ATP in the energy-conversion system coupled to photosynthetic electron transport. 2. A significant amount of ATP is synthesized when a reaction mixture containing chromatophores and ADP is illuminated and then incubated with P(i) in the dark. ATP is not synthesized to an appreciable extent, either when a reaction mixture containing chromatophores and P(i) is illuminated and then incubated with ADP in the dark, or when one containing chromatophores alone is illuminated and then incubated with ADP and P(i) in the dark. The amount of ATP thus synthesized is influenced markedly by concentrations of ADP. 3. The chromatophores illuminated with ADP, if allowed to stand in the dark at 30 degrees , gradually lose the ability to form ATP with P(i) in the dark. No loss of the ability occurs when the chromatophores illuminated with ADP are allowed to stand in the dark at 13 degrees or in a frozen state. 4. Mg(2+) is absolutely required for chromatophores to form ATP in the dark after illumination in the presence of ADP, and for the chromatophores to achieve ATP formation with P(i) in the dark. 5. Antimycin A, 2-heptyl-4-hydroxyquinoline N-oxide and o-phenanthroline strongly inhibit the light-dependent acquisition of the ability to form ATP with P(i) in the dark, but not the consequent ATP formation with P(i) in the dark. Arsenate, 2,4-dinitrophenol, quinacrine hydrochloride, quinine hydrochloride and pyrophosphate inhibit the former or the latter, or both. Oligomycin inhibits the former somewhat more than the latter. 6. From these findings it is suggested that a high-energy intermediate is formed in photosynthetic ATP formation, and that its formation is dependent on ADP but not P(i).

MeSH Terms
Adenine Nucleotides/metabolism Adenosine Triphosphate/biosynthesis Antimycin A/pharmacology Ascorbic Acid/pharmacology Bacterial Chromatophores/metabolism Hydrogen-Ion Concentration In Vitro Techniques Light Magnesium/metabolism Oligomycins/pharmacology Phenanthrolines/pharmacology Phenazines/pharmacology Quinolines/pharmacology Rhodospirillum/metabolism
Chemicals
Adenine Nucleotides Oligomycins Phenanthrolines Phenazines Quinolines Antimycin A Adenosine Triphosphate Magnesium Ascorbic Acid
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Horio T
Nishikawa K
Yamashita J
References (16)
16 references, click to expand
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1966-01-00
Pages
321-9
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1264834
Subset
IM
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