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  • 1
    ISSN: 1432-2048
    Keywords: C3, C4 plants (H-isotope composition) ; Deuterium ; Hydrogen-isotope composition ; Leaf (H-isotope composition)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The natural abundance hydrogen-isotope composition of leaf water ( $$\delta _{\text{D}}^{{\text{H}}_{\text{2}} {\text{O}}} $$ ) and leaf organic matter (δ D org ) was measured in leaves of C3 and C4 dicotyledons and monocotyledons. The $$\delta _{\text{D}}^{{\text{H}}_{\text{2}} {\text{O}}} $$ value of leaf water showed a marked diurnal variation, greatest enrichment being observed about midday. However, this variation was greater in the more slowly transpiring C4 plants than in C3 plants under comparable environmental conditions. A model based on analogies with a constant feed pan of evaporating water was developed and the difference between C3 and C4 plants expressed in terms of either differences in kinetic enrichment or different leaf morphology. Microclimatic and morphological features of the leaves which may be associated with this factor are discussed. There was no daily excursion in the δ D org value in leaves of either C3 or C4 plants. When δ D org values were referenced to the mean $$\delta _{\text{D}}^{{\text{H}}_{\text{2}} {\text{O}}} $$ values during the period of active photosynthesis, the discrimination against deuterium during photosynthetic metabolism (ΔD) was greater in C3 plants (-117 to -121‰) than in C4 plants (-86 to -109‰). These results show that the different water use “strategies” of C3 and C4 plants are responsible for the measured difference in deuterium-isotope composition of leaf water. However, it is unlikely that these physical processes account fully for the differences in hydrogen-isotope composition of the products of C3 and C4 photosynthetic metabolism.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-5079
    Keywords: chlorophyll fluorescence ; herbicide binding ; photoinhibition ; photosynthesis ; photosystem II ; temperature
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The time courses of some Photosystem II (PS II) parameters have been monitored during in-vivo and in-vitro photoinhibition of spinach chloroplasts, at room temperature and at 10 °C or 0 °C. Exposing leaf discs of low-light grown spinach at 25 °C to high light led to photoinhibition of chloroplasts in-vivo as manifested by a parallel decrease in the number of functional PS II centres, the variable chlorophyll fluorescence at 77K (F v /F m ), and the number of atrazine-binding sites. When the photoinhibitory treatment was given at 10 °C, the former two parameters declined in parallel but the loss of atrazine-binding sites occurred more slowly and to a lesser extent. During in-vitro photoinhibition of chloroplast thylakoids at 25 °C, the loss of functional PS II centres proceeded slightly more rapidly than the loss of atrazine-binding sites, and this difference in rate was further increased when the thylakoids were photoinhibited at 0 °C. During the recovery phase of leaf discs (up to 9 h) the increases in F v /F m preceded that of the number of functional PS II centres, while only a further decline in the number of atrazine-binding sites was observed. The recovery of variable chlorophyll fluorescence and the concentration of functional PS II centres occurred more rapidly at 25 °C than at 10 °C. These results suggest that the photoinhibition of PS II function is a relatively temperature-independent early photochemical event, whereas the changes in the concentration of herbicide-binding sites appear to be a more complex biochemical process which can occur with a delayed time course.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-5028
    Keywords: chloroplast protein synthesis ; D1 ; LSU ; photoinhibition ; translational regulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Transfer of Chlamydomonas reinhardtii cells grown photoautotrophically in low light to higher light intensities has a dramatic transient effect on the differential expression of the two major chloroplast encoded photosynthetic proteins. Synthesis of the D1 protein of Photosystem II increases more than 10-fold during the first six hours in high light (HL), whereas synthesis of the large subunit (LSU) of Rubisco drops dramatically within 15 min and only gradually resumes at about 6 h. Synthesis of the chloroplast-encoded ATP synthaseβ subunit, the nuclear-encoded Rubisco small subunit and the nuclear-encoded β-tubulin is not noticeably affected. Up regulation of psbA mRNA translation accounts for a substantial fraction of the increased D1 synthesis, since accumulation of psbA mRNA increases 4.2- and 6.3-fold less than D1 synthesis at 6 and 18 h in HL. Down-regulation of LSU synthesis is not correlated with a reduction in the steady-state level of the rbcL transcript. Primer extension mapping of the 5' ends of the rbcL mRNAs reveals transcripts with start points located at -93 and -186 relative to the first translated ATG. Transfer of low light (LL)-grown cells to HL temporarily decreases the ratio of the -93 to -186 transcripts, but this ratio normalizes after 6 h in HL, coincident with the recovery in the synthesis of LSU. These several distinct effects of temporary light stress were correlated with a rapid, sustained increase in the reduction state of QA, a transient decline in photosynthetic efficiency, a less rapid drop in total chlorophyll content and a delay in cell division.
    Type of Medium: Electronic Resource
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