Abstract
The Chlamydomonas reinhardtii mutant FUD50 has a deletion in the atpB gene of the chloroplast ATP synthase [Woessner, J. P., Masson, A., Harris, E. H., Bennoun, P., Gillham, N. W., and Boynton, J. E. (1984) Plant Mol. Biol. 3, 177-190]. We have isolated a suppressed strain (FUD50su) that can grow under phototrophic conditions, although it still showed no synthesis of the beta subunit of coupling factor 1. Thylakoid membranes of the FUD50su strain were similar to those of the original FUD50 strain, in that they both lacked all the subunits making up the chloroplast ATP synthase complex. We show that photosynthesis in FUD50su is sensitive to inhibitors such as antimycin, specific for mitochondrial electron transport. This observation indicates that photosynthesis in the FUD50su strain is achieved through an unusual interaction between mitochondria and chloroplast. Exportation of light-induced reduced compounds from the chloroplast to the mitochondria elicits ATP formation in the latter, and ATP is subsequently imported to the chloroplast. The activation of such an ATP shuttle coupled to an NADPH shuttle would thus provide the reducing power and the free energy needed for carbon assimilation in a chloroplast that lacks chloroplast ATP synthase.
Full text
PDF




Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bennoun P. Evidence for a respiratory chain in the chloroplast. Proc Natl Acad Sci U S A. 1982 Jul;79(14):4352–4356. doi: 10.1073/pnas.79.14.4352. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chua N. H., Bennoun P. Thylakoid membrane polypeptides of Chlamydomonas reinhardtii: wild-type and mutant strains deficient in photosystem II reaction center. Proc Natl Acad Sci U S A. 1975 Jun;72(6):2175–2179. doi: 10.1073/pnas.72.6.2175. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chua N. H., Gillham N. W. The sites of synthesis of the principal thylakoid membrane polypeptides in Chlamydomonas reinhardtii. J Cell Biol. 1977 Aug;74(2):441–452. doi: 10.1083/jcb.74.2.441. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ikuma H., Bonner W. D. Properties of Higher Plant Mitochondria. I. Isolation and Some Characteristics of Tightly-coupled Mitochondria from Dark-grown Mung Bean Hypocotyls. Plant Physiol. 1967 Jan;42(1):67–75. doi: 10.1104/pp.42.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Joliot P., Delosme R. Flash-induced 519 nm absorption change in green algae. Biochim Biophys Acta. 1974 Aug 23;357(2):267–284. doi: 10.1016/0005-2728(74)90066-8. [DOI] [PubMed] [Google Scholar]
- Junge W., Rumberg B., Schröder H. The necessity of an electric potential difference and its use for photophosphorylation in short flash groups. Eur J Biochem. 1970 Jul;14(3):575–581. doi: 10.1111/j.1432-1033.1970.tb00326.x. [DOI] [PubMed] [Google Scholar]
- Junge W., Witt H. T. On the ion transport system of photosynthesis--investigations on a molecular level. Z Naturforsch B. 1968 Feb;23(2):244–254. doi: 10.1515/znb-1968-0222. [DOI] [PubMed] [Google Scholar]
- Kelly G. J., Gibbs M. A mechanism for the indirect transfer of photosynthetically reduced nicotinamide adenine dinucleotide phosphate from chloroplasts to the cytoplasm. Plant Physiol. 1973 Dec;52(6):674–676. doi: 10.1104/pp.52.6.674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klingenberg M. The ADP-ATP translocation in mitochondria, a membrane potential controlled transport. J Membr Biol. 1980 Sep 30;56(2):97–105. doi: 10.1007/BF01875961. [DOI] [PubMed] [Google Scholar]
- Levine R. P. Genetic dissection of photosynthesis. Science. 1968 Nov 15;162(3855):768–771. doi: 10.1126/science.162.3855.768. [DOI] [PubMed] [Google Scholar]
- Mitchell P. Chemiosmotic coupling in oxidative and photosynthetic phosphorylation. Biol Rev Camb Philos Soc. 1966 Aug;41(3):445–502. doi: 10.1111/j.1469-185x.1966.tb01501.x. [DOI] [PubMed] [Google Scholar]
- Nelson N., Nelson H., Schatz G. Biosynthesis and assembly of the proton-translocating adenosine triphosphatase complex from chloroplasts. Proc Natl Acad Sci U S A. 1980 Mar;77(3):1361–1364. doi: 10.1073/pnas.77.3.1361. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Piccioni R. G., Bennoun P., Chua N. H. A nuclear mutant of Chlamydomonas reinhardtii defective in photosynthetic photophosphorylation. Characterization of the algal coupling factor ATPase. Eur J Biochem. 1981 Jun;117(1):93–102. doi: 10.1111/j.1432-1033.1981.tb06307.x. [DOI] [PubMed] [Google Scholar]
- Pick U., Racker E. Purification and reconstitution of the N,N'-dicyclohexylcarbodiimide-sensitive ATPase complex from spinach chloroplasts. J Biol Chem. 1979 Apr 25;254(8):2793–2799. [PubMed] [Google Scholar]
- Robinson S. P., Wiskich J. T. Pyrophosphate inhibition of carbon dioxide fixation in isolated pea chloroplasts by uptake in exchange for endogenous adenine nucleotides. Plant Physiol. 1977 Mar;59(3):422–427. doi: 10.1104/pp.59.3.422. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rumberg B., Siggel U. Quantitative Zusammenhänge zwischen Chlorophyll-b-Reaktion, Elektronentransport und Phosphorylierung bei der Photosynthese. Z Naturforsch B. 1968 Feb;23(2):239–244. [PubMed] [Google Scholar]
- Salerno J. C., Harmon H. J., Blum H., Leigh J. S., Ohnishi T. A transmembrane quinone pair in the succinate dehydrogenase--cytochrome b region. FEBS Lett. 1977 Oct 15;82(2):179–182. doi: 10.1016/0014-5793(77)80579-6. [DOI] [PubMed] [Google Scholar]
- Slater E. C. The mechanism of action of the respiratory inhibitor, antimycin. Biochim Biophys Acta. 1973 Dec 7;301(2):129–154. doi: 10.1016/0304-4173(73)90002-5. [DOI] [PubMed] [Google Scholar]
- Thierbach G., Reichenbach H. Myxothiazol, a new inhibitor of the cytochrome b-c1 segment of th respiratory chain. Biochim Biophys Acta. 1981 Dec 14;638(2):282–289. doi: 10.1016/0005-2728(81)90238-3. [DOI] [PubMed] [Google Scholar]
- Vignais P. V. Molecular and physiological aspects of adenine nucleotide transport in mitochondria. Biochim Biophys Acta. 1976 Apr 30;456(1):1–38. doi: 10.1016/0304-4173(76)90007-0. [DOI] [PubMed] [Google Scholar]
- Woessner J. P., Gillham N. W., Boynton J. E. The sequence of the chloroplast atpB gene and its flanking regions in Chlamydomonas reinhardtii. Gene. 1986;44(1):17–28. doi: 10.1016/0378-1119(86)90038-7. [DOI] [PubMed] [Google Scholar]

