M. Kitajima

Bio: M. Kitajima is an academic researcher from University of California, San Diego. The author has contributed to research in topics: Photosystem I & P700. The author has an hindex of 5, co-authored 6 publications receiving 1523 citations.

Microencapsulation of Chloroplast Particles

Abstract: Chloroplast and photosystem I particles were encapsulated in small spheres (about 20 mum diameter) with an artificial membrane built up by cross-linking amino groups of protamine with toluenediisocyanate. The artificial membrane was permeable to small substrate and product molecules but not to soluble proteins. Photosystem I activity was retained by the encapsulated chloroplast particles. Washed photosystem I particles were encapsulated with the soluble proteins, ferredoxin, and ferredoxin-NADP oxidoreductase, and the microcapsules photoreduced NADP using ascorbate plus dichlorophenolindophenol as the electron donor. The photosystem I particles were also encapsulated with hydrogenase from Chromatium and a very low rate of photoevolution of hydrogen was obtained. The results show that chloroplast membrane fragments can be encapsulated with soluble proteins that couple transfer reactions to the primary photochemical apparatus.

Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins.

Abstract: Photon yields of oxygen evolution at saturating CO2 were determined for 44 species of vascular plants, representing widely diverse taxa, habitats, life forms and growth conditions. The photonyield values on the basis of absorbed light (φa) were remarkably constant among plants possessing the same pathway of photosynthetic CO2 fixation, provided the plants had not been subjected to environmental stress. The mean φa value ±SE for 37 C3 species was 0.106±0.001 O2·photon-1. The five C4 species exhibited lower photon yields and greater variation than the C3 species (φa=0.0692±0.004). The φa values for the two Crassulaceanacid-metabolism species were similar to those of C3 species. Leaf chlorophyll content had little influence on φa over the range found in normal, healthy leaves. Chlorophyll fluorescence characteristics at 77 K were determined for the same leaves as used for the photon-yield measurements. Considerable variation in fluorescence emission both at 692 nm and at 734 nm, was found 1) among the different species; 2) between the upper and lower surfaces of the same leaves; and 3) between sun and shade leaves of the same species. By contrast, the ratio of variable to maximum fluorescence emission at 692 nm (Fv/FM, 692) remained remarkably constant (The mean value for the C3 species was 0.832±0.004). High-light treatments of shade leaves resulted in a reduction in both φa and the Fv/FM, 692 ratio. The extent of the reductions increased with time of exposure to bright light. A linear relationship was obtained when φa was plotted against Fv/FM, 692. The results show that determinations of the photon yield of O2 evolution and the Fv/FM, 692 ratio can serve as excellent quantitative measures of photoinhibition of overall photosynthetic energy-conversion system and of photochemistry of photosystem II, respectively. This is especially valuable in field work where it is often impossible to obtain appropriate controls.

The use of chlorophyll fluorescence nomenclature in plant stress physiology.

Abstract: During recent years there has been remarkable progress in the understanding and practical use of chlorophyll fluorescence in plant science. This 'renaissance' of chlorophyll fluorescence was induced by the urgent need of applied research (like plant stress physiology, ecophysiology, phytopathology etc.) for quantitative, non-invasive, rapid methods to assess photosynthesis in intact leaves. Recent developments of suitable instrumentation and methodology have substantially increased these possibilities. Actually, a vast amount of knowledge on chlorophyll fluorescence had already accumulated over more than 50 years, since the discovery of the Kautsky effect in 1931 (Kautsky and Hirsch 1931) (for reviews, see e.g., Lavorel and Etienne 1977, Briantais et al. 1986, Renger and Schreiber 1986). On the one hand this knowledge was mechanistic, resulting from biophysically oriented basic research. On the other hand it was phenomenological, originating from applied plant physiological research. Until recently the phenomenology of whole leaf chlorophyll fluorescence appeared far too complex to find serious attention of biophysicists. Thus, for a long time, there was a gap between applied and basic research in chlorophyll fluorescence. Developments in instrumentation (Ogren and Baker 1985, Schreiber 1986, Schreiber et al. 1986) and methodology (Bradbury and Baker 1981, Krause et al. 1982, Quick and Horton 1984, Dietz et al. 1985, Demmig et al. 1987, Weis and Berry 1987, Bilger et al. 1989, Genty et al. 1989) has succeeded in closing this gap and bringing these two disciplines into sufficiently close contact and in mutually stimulating interaction. Consequently the present "renaissance" of chlorophyll fluorescence may be the product of a fruitful dynamic interaction between three different research disciplines, i.e., basic and applied research linked to new developments in instrumentation and methodology (see scheme in Fig. 1). As a result, measuring chlorophyll fluorescence has become a very attractive means of obtaining rapid, semiquantitative information on photosynthesis, used by an increasing number of researchers not only in the laboratory but also in the field. The wide range of possible applications is reflected by the broad spectrum of contributions to this issue of Photosynthesis Research. The progress made in chlorophyll fluorescence instrumentation and methodology has also induced new developments in the adjacent fields of absorbance spectroscopy (e.g., Klughammer et al. or Harbinson et al. in this issue), photoacoustic spectroscopy (e.g., Canaani, Dau and Hansen, Kolbowski et al. or Snel et al. in this issue) and chlorophyll luminescence (delayed fluorescence) (Bilger and Schreiber in this issue). These new developments are expected to play a role in

Regulation of light harvesting in green plants

Abstract: When plants are exposed to light intensities in excess of those that can be utilized in photosynthetic electron transport, nonphotochemical dissipation of excitation energy is induced as a mechanism for photoprotection of photosystem II. The features of this process are reviewed, particularly with respect to the molecular mechanisms involved. It is shown how the dynamic properties of the proteins and pigments of the chlorophyll a/b light-harvesting complexes of photosystem II first enable the level of excitation energy to be sensed via the thylakoid proton gradient and subsequently allow excess energy to be dissipated as heat by formation of a nonphotochemical quencher. The nature of this quencher is discussed, together with a consideration of how the variation in capacity for energy dissipation depends on specific features of the composition of the light-harvesting system. Finally, the prospects for future progress in understanding the regulation of light harvesting are assessed.