Abstract
Bundle sheath and mesophyll chloroplasts from Zea mays showed comparable rates of O2 evolution, which amounted to about half of the rate observed in spinach (Spinacia oleracea) chloroplasts.
Ratios of 4.5, 4.6, and 6.2 Mn2+ atoms per 400 chlorophylls were observed in mesophyll, bundle sheath, and spinach chloroplasts, respectively. These ratios roughly correspond to the observed O2 evolution rates.
Rates of electron transport from water to methylviologen (photosystem I and II) in both types of corn chloroplasts were about one-third that in spinach. Compared to spinach, transport rates from reduced diaminodurene to methylviologen (photosystem I) were about one-third and greater than one-half in mesophyll and bundle sheath material, respectively.
In both types of corn chloroplasts, electron flow from photosystem II to P700 was abnormal. This observation, together with the low rates of all activities, suggests that damage occurred during isolation. Such damage may limit the quantitative significance of observations made with these materials (including the following data).
Measurements of flash yields of O2 evolution or O2 uptake showed that the size of the photosynthetic unit was the same in photosystems I and II and in all three types of chloroplasts (about 400 chlorophylls per equivalent).
Similarity of the photochemical cross-section of the two photosystems in the three preparations was also found in optical experiments: that is the half-times of the fluorescence rise in the presence of 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU) (photosystem II) and of the photooxidation of P700 (photosystem I).
The ratio of P700 to chlorophyll appeared to be about 2-fold higher in bundle sheath chloroplasts than in the other materials (1/200 versus 1/400).
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Selected References
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- Andersen K. S., Bain J. M., Bishop D. G., Smillie R. M. Photosystem II Activity in Agranal Bundle Sheath Chloroplasts from Zea mays. Plant Physiol. 1972 Apr;49(4):461–466. doi: 10.1104/pp.49.4.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Anderson J. M., Boardman N. K., Spencer D. Phosphorylation by intact bundle sheath chloroplasts from maize. Biochim Biophys Acta. 1971 Aug 6;245(1):253–258. doi: 10.1016/0005-2728(71)90032-6. [DOI] [PubMed] [Google Scholar]
- Anderson J. M., Woo K. C., Boardman N. K. Photochemical systems in mesophyll and bundle sheath chloroplasts of C 4 plants. Biochim Biophys Acta. 1971 Sep 7;245(2):398–408. doi: 10.1016/0005-2728(71)90158-7. [DOI] [PubMed] [Google Scholar]
- Arnon D. I. COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS. Plant Physiol. 1949 Jan;24(1):1–15. doi: 10.1104/pp.24.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bazzaz M. B., Govindjee Photochemical properties of mesophyll and bundle sheath chloroplasts of maize. Plant Physiol. 1973 Sep;52(3):257–262. doi: 10.1104/pp.52.3.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bishop D. G. Lamellar structure and composition of chloroplasts in relation to photosynthetic electron transfer. Photochem Photobiol. 1974 Sep;20(3):281–299. doi: 10.1111/j.1751-1097.1974.tb06579.x. [DOI] [PubMed] [Google Scholar]
- Cheniae G. M., Martin I. F. Photoreaction of manganese catalyst in photosynthetic oxygen evolution. Plant Physiol. 1969 Mar;44(3):351–360. doi: 10.1104/pp.44.3.351. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Doschek W. W., Kok B. Photon trapping in photosystem II of photosynthesis. The fluorescence rise curve in the presence of 3-(3,4-dichlorophenyl)-1,1-dimetnhylurea. Biophys J. 1972 Jul;12(7):832–838. doi: 10.1016/s0006-3495(72)86126-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hardt H., Kok B. Plastocyanin as the possible site of photosynthetic electron transport inhibition by glutaraldehyde. Plant Physiol. 1977 Aug;60(2):225–229. doi: 10.1104/pp.60.2.225. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hiyama T., Ke B. Difference spectra and extinction coefficients of P 700 . Biochim Biophys Acta. 1972 Apr 20;267(1):160–171. doi: 10.1016/0005-2728(72)90147-8. [DOI] [PubMed] [Google Scholar]
- Malkin S., Kok B. Fluorescence induction studies in isolated chloroplasts. I. Number of components involved in the reaction and quantum yields. Biochim Biophys Acta. 1966 Nov 8;126(3):413–432. doi: 10.1016/0926-6585(66)90001-x. [DOI] [PubMed] [Google Scholar]
- Marsho T. V., Kok B. Interaction between electron transport components in chloroplasts. Biochim Biophys Acta. 1970 Dec 8;223(2):240–250. doi: 10.1016/0005-2728(70)90181-7. [DOI] [PubMed] [Google Scholar]
- Mayne B. C. Spectral, Physical, and Electron Transport Activities in the Photosynthetic Apparatus of Mesophyll Cells and Bundle Sheath Cells of Digitaria sanguinalis (L.) Scop. Plant Physiol. 1971 May;47(5):600–605. doi: 10.1104/pp.47.5.600. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Myers J., Graham J. R. Photosynthetic Unit Size during the Synchronous Life Cycle of Scenedesmus. Plant Physiol. 1975 Apr;55(4):686–688. doi: 10.1104/pp.55.4.686. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Radmer R., Kok B. A kinetic analysis of the oxidizing and reducing sides of the O2-evolving system of photosynthesis. Biochim Biophys Acta. 1973 Jul 26;314(1):28–41. doi: 10.1016/0005-2728(73)90061-3. [DOI] [PubMed] [Google Scholar]
- Schwartz M. N-tetramethyl-rho-phenylenediamine as a catalyst of photophosphorylation. Biochim Biophys Acta. 1966 Feb 7;112(2):204–212. doi: 10.1016/0926-6585(66)90321-9. [DOI] [PubMed] [Google Scholar]
- Woo K. C., Anderson J. M., Boardman N. K., Downton W. J., Osmond C. B., Thorne S. W. Deficient Photosystem II in Agranal Bundle Sheath Chloroplasts of C(4) Plants. Proc Natl Acad Sci U S A. 1970 Sep;67(1):18–25. doi: 10.1073/pnas.67.1.18. [DOI] [PMC free article] [PubMed] [Google Scholar]
