Biomedical subjects

S. Rodermel

Publications and source records attributed to S. Rodermel.

3 recordsLinked to original sources

PubMed1997

Elevated CO2 Effects during Leaf Ontogeny (A New Perspective on Acclimation).

For many plants growth in elevated CO2 leads to reduced rates of photosynthesis. To examine the role that leaf ontogeny plays in the acclimation response, we monitored photosynthesis and some related parameters at short intervals throughout the ontogenetic development of tobacco (Nicotiana tabacum L.) leaves under ambient (350 [mu]L L-1)- and high (950 [mu]L L-1)-CO2 conditions. The pattern of photosynthetic rate over time was similar between the two treatments and consistent with the expected pattern for a typical dicot leaf. However, the photosynthesis pattern in high-CO2-grown tobacco was shifted temporally to an earlier maximum and subsequent senescent decline. Ribulose-1,5-biphosphate carboxylase/oxygenase activity appeared to be the main factor regulating photosynthetic rates in both treatments. Therefore, we propose a new model for interpreting the acclimation response. Lowered photosynthetic rates observed during acclimation appear to be the result of a shift in the timing of the normal photosynthetic stages of leaf ontogeny to an earlier onset of the natural decline in photosynthetic rates associated with senescence.

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PubMed1997

Source Strength Regulates an Early Phase Transition of Tobacco Shoot Morphogenesis.

We have taken advantage of specific reductions in the ribulose-1,5-bisphosphate carboxylase/oxygenase concentration in rbcS antisense mutants of tobacco (Nicotiana tabacum L.) to assess the contribution of source strength (carbohydrate production) to the control of shoot development. Wild-type and antisense plants undergo distinct phases of shoot development that can be distinguished from one another on the basis of differences in stem elongation rates, internode distances, plastochron indices, leaf sizes, and leaf morphologies. An early phase of shoot morphogenesis is markedly prolonged in the antisense plants, and an increased number of leaves emerge during this phase in the mutants. This delay is specific, inasmuch as the duration and expression of traits characteristic of later phases of shoot development proceed normally. In addition to altered shoot developmental patterns, the antisense mutants have enhanced shoot/root ratios and markedly increased leaf longevities. It is likely that these are adaptations that enhance photosynthetic rates. Consistent with this proposal, the total leaf areas and dry weights of the mutant and wild type are similar at flowering. Collectively, our results indicate that source strength regulates the duration of an early phase of tobacco shoot development and the transition to a later phase. We suggest that this phase change may occur in response to the attainment of a threshold source strength, which is delayed in the mutant plants.

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PubMed1996

Lhcb Transcription Is Coordinated with Cell Size and Chlorophyll Accumulation (Studies on Fluorescence-Activated, Cell-Sorter-Purified Single Cells from Wild-Type and immutans Arabidopsis thaliana).

To study the mechanisms that integrate pigment and chlorophyll a/b-binding apoprotein biosynthesis during light-harvesting complex II assembly, we have examined [beta]-glucuronidase (GUS) enzyme activities, chlorophyll contents, and cell sizes in fluorescence-activated, cell-sorting-separated single cells from transgenic Arabidopsis thaliana wild-type and immutans variegation mutant plants that express an Lhcb (photosystem II chlorophyll a/b-binding polypeptide gene)/GUS promoter fusion. We found that GUS activities are positively correlated with chlorophyll content and cell size in green cells from the control and immutans plants, indicating that Lhcb gene transcription is coordinated with cell size in this species. Compared with the control plants, however, chlorophyll production is enhanced in the green cells of immutans; this may represent part of a strategy to maximize photosynthesis in the green sectors to compensate for a lack of photosynthesis in the white sectors of the mutant. Lhcb transcription is significantly higher in pure-white cells of the transgenic immutans plants than in pure-white cells from norflurazon-treated, photooxidized A. thaliana leaves. This suggests that immutans partially uncouples Lhcb transcription from its normal dependence on chlorophyll accumulation and chloroplast development. We conclude that immutans may play a role in regulating Lhcb transcription, and may be a key component in the signal transduction pathways that control chloroplast biogenesis.

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