Grimmia homodictyon Dixon

Abstract

We examined photosynthetic responses of two dominant pleurocarpous mosses, Actinothuidium hookeri (Mitt.) Broth. and Hylocomium splendens (Hedw.) Schimp. to low-level nitrogen (N) addition. The study was conducted in an old-growth fir forest on the eastern Tibetan Plateau. The added N, 1 g N/m², was mainly absorbed by the new-growth. The concentrations of chlorophyll a and b both increased 8 days after N addition. The quantum yield of Photosystem II (Φ_PSII) also increased. However, no significant changes were found in terms of gas exchange parameters. The mass-based CO₂ assimilation rate, chlorophyll a content, and chlorophyll a/b ratio (which is related to antenna size of the photosystem), of H. splendens were all higher than those of A. hookeri. Shoot mass per area (SMA) of H. splendens was lower than that of A. hookeri. We conclude that the photosynthetic rate was less sensitive to low-level N addition than chlorophyll contents and chlorophyll fluorescence parameters, suggesting other limiting factors in the photosynthetic process. Additionally, the faster growing H. splendens has a higher photosynthetic capacity than A. hookeri, allocating fewer resources to structural tissue.     

Evolutionary Changes in Chlorophyllide a Oxygenase (CAO) Structure Contribute to the Acquisition of a New Light-harvesting Complex in Micromonas

Chlorophyll b is found in photosynthetic prokaryotes and primary and secondary endosymbionts, although their light-harvesting systems are quite different. Chlorophyll b is synthesized from chlorophyll a by chlorophyllide a oxygenase (CAO), which is a Rieske-mononuclear iron oxygenase. Comparison of the amino acid sequences of CAO among photosynthetic organisms elucidated changes in the domain structures of CAO during evolution. However, the evolutionary relationship between the light-harvesting system and the domain structure of CAO remains unclear. To elucidate this relationship, we investigated the CAO structure and the pigment composition of chlorophyll-protein complexes in the prasinophyte Micromonas. The Micromonas CAO is composed of two genes, MpCAO1 and MpCAO2, that possess Rieske and mononuclear iron-binding motifs, respectively. Only when both genes were introduced into the chlorophyll b-less Arabidopsis mutant (ch1-1) was chlorophyll b accumulated, indicating that cooperation between the two subunits is required to synthesize chlorophyll b. Although Micromonas has a characteristic light-harvesting system in which chlorophyll b is incorporated into the core antennas of reaction centers, chlorophyll b was also incorporated into the core antennas of reaction centers of the Arabidopsis transformants that contained the two Micromonas CAO proteins. Based on these results, we discuss the evolutionary relationship between the structures of CAO and light-harvesting systems.     

四种重楼属植物光合作用特征

Species of Paris (Trilliaceae) have often been used as medicinal plants. Because of excessive exploitation,in this regard the wild resource of Paris is almost exhausted. Some species of Paris were transplanted for use in photosynthesis research and for conservation purposes. In the present study, light and CO2 photosynthetic response curves were investigated in four Paris taxa: P.polyphylla var. yunnanensis and var. alba, P.mairei, and P.marmorata. Our results showed that P.marmorata had the highest maximum photosynthetic rate (Pmax; 8.6μmol·m-2·s-1), light saturation point (LSP; 827μmol·m-2·s-1), maximum electron transport rate (Jmax; 39.9mol·m-2·s-1), a relatively high maximum carboxylation rate (Vcmax; 28.9μmol·m-2·s-1) and carbon dioxide saturation point (Cisat; 726μmol·mol-1), but a lower light compensation point (LCP; 6.23μmol·m-2·s-1) and the lowest carbon dioxide compensation point (Г*; 20.7μmol·mol-1). This suggests that P.marmorata is well adapted to light and CO2; however it has a low ability to acclimate to environmental stress as indicated by low water use efficiency (WUE) in high light conditions. P.polyphylla var. yunnanensis had the highest light compensation point (LCP; 10.1μmol·m-2·s-1), carbon dioxide compensation point (Г*; 35.3μmol·mol-1), carbon dioxide saturation point (Cisat; 727μmol·mol-1), relatively high maximum photosynthetic rate (Pmax; 7.5μmol·m-2·s-1) and light saturation point (LSP; 728μmol·m-2·s-1), maximum light saturated electron transfer rate (Jmax; 37.7μmol·m-2·s-1), suggesting that it is suitable for conditions of higher light and CO2 concentration. This taxon can adapt to adverse conditions, as suggested by high WUE under increased CO2 concentration. In contrast, P.polyphylla var. alba exhibited a relatively lower apparent quantum yield (AQY; 0.037μmol·mol-1) and poorer growth performance than the other taxa. We suggest from our results that different light and water conditions are suitable for the growth of the different taxa. Photosynthesis assimilation efficiency and production can be increased by raising humidity for P.polyphylla var. yunnanensis and P.marmorata. To protect plants of P.polyphylla var. alba from strong sunshine, they should be shaded from March to mid June.     

GA3和Spd对杜鹃开花期光合特性和抗氧化系统的影响

为探讨GA_3和Spd对杜鹃(Rhododendron simsii)开花花期和开花品质的影响,研究了外源GA_3和Spd对杜鹃开花期光合特性和抗氧化系统的变化。结果表明,外源GA_3对花期有显著的提前作用,Spd对花期有明显的延迟作用,但两者均使花期延长、花径增大且成花率提高。GA_3和Spd处理提高了花期叶片的光合色素含量和净光合速率(Pn)、气孔导度(Gs)和胞间CO_2浓度(Ci);GA_3处理提高了叶片的蒸腾速率(Tr),而Spd使叶片的Tr下降,两者均有效缓解了末花期叶绿素含量的下降。GA_3和Spd处理显著降低了花瓣MDA含量,提高了抗氧化酶SOD、POD和CAT活性,并减缓了末花期SOD的下降,有效延缓了衰老进程,延长花期。以1 600 mg L~(–1) GA_3和0.10 mmol L~(-1) Spd处理效果较好,能有效提高杜鹃花的观赏品质。     

Contribution of NDH-dependent cyclic electron transport around photosystem I to the generation of proton motive force in the weak mutant allele of pgr5

In angiosperms, cyclic electron transport (CET) around photosystem I (PSI) consists of two pathways, depending on PGR5/PGRL1 proteins and the chloroplast NDH complex. In single mutants defective in chloroplast NDH, photosynthetic electron transport is only slightly affected at low light intensity, but in double mutants impaired in both CET pathways photosynthesis and plant growth are severely affected. The question is whether this strong mutant phenotype observed in double mutants can be simply explained by the additive effect of defects in both CET pathways. In this study, we used the weak mutant allele of pgr5-2 for the background of double mutants to avoid possible problems caused by the secondary effects due to the strong mutant phenotype. In two double mutants, crr2-2 pgr5-2 and ndhs-1 pgr5-2, the plant growth was unaffected and linear electron transport was only slightly affected. However, NPQ induction was more severely impaired in the double mutants than in the pgr5-2 single mutant. A similar trend was observed in the size of the proton motive force. Despite the slight reduction in photosystem II parameters, PSI parameters were severely affected in the pgr5-2 single mutant, the phenotype that was further enhanced by adding the NDH defects. Despite the lack of ?pH-dependent regulation at the cytochrome b₆f complex (donor-side regulation of PSI), the plastoquinone pool was more reduced in the double mutants than in the pgr5-2 single mutants. This phenotype suggests that both PGR5/PGRL1- and NDH-dependent CET contribute to supply sufficient acceptors from PSI by balancing the ATP/NADPH production ratio.     

Calphostin C induces tyrosine dephosphorylation/inactivation of protein kinase Fa/GSK-3α in a pathway independent of tumor promoter phorbol ester-mediated down-regulation of protein kinase C

The signal transduction mechanism of protein kinase FA /GSK-3α by tyrosine phosphorylation in A431 cells was investigated using calphostin C as an inhibitor for protein kinase C (PKC). Kinase Fa /GSK-3α could be tyrosine-dephosphorylated and inactivated to ∼ 10% of control in a concentration-dependent manner by 0.1–10 μM calphostin C (IC₅₀, ∼ 1 μM), as demonstrated by immunoprecipitation of kinase Fa /GSK-3α from cell extracts, followed by phosphoamino acid analysis and by immunodetection in an antikinase Fa /GSK-3α immunoprecipitate kinase assay. In sharp contrast, down-regulation of PKC by 0.05 μM calphostin C (IC₅₀, ∼ 0.05 μM for inhibiting PKC in cells) or by tumor promoter phorbol ester TPA was found to have stimulatory effect on the cellular activity of kinase Fa /GSK-3α, when processed under identical conditions. Furthermore, TPA-mediated down-regulation of PKC was found to have no effect on calphostin C-mediated tyrosine dephosphorylation/inactivation of kinase Fa /GSK-3α. Taken together, the results provide initial evidence that the PKC inhibitor calphostin C may induce tyrosine dephosphorylation/inactivation of kinase Fa /GSK-3α in a pathway independent of TPA-mediated down-regulation of PKC, representing a new mode of signal transduction for the regulation of this multisubstrate/multifunctional protein kinase by calphostin C in cells. Since kinase Fa /GSK-3α is a possible carcinoma dedifferentiation/progression-promoting factor, the results further suggest calphostin C as a potential anticancer drug involved in blocking carcinoma dedifferentiation/progression, possibly via inactivation of protein kinase FA /GSK-3α in tumor cells. © 1996 Wiley-Liss, Inc.     

珍珠芦荟失绿突变体‘MT-1’的农艺性状、解剖结构、光合特性和代谢组特征分析

为阐明珍珠芦荟叶色突变的变异机制, 以珍珠芦荟(Aristaloe aristata)叶色失绿突变体‘MT-1’及其叶色正常种质‘WT-18’为试材,对其表型特征、叶片超微结构、光合色素含量、叶绿素荧光参数、差异代谢产物等方面进行了对比研究。结果表明, 与‘WT-18’相比,突变体‘MT-1’从幼叶开始呈现出黄化条斑现象,且株型变小、生长缓慢;气孔数量少且小,形状由长方形变成正方形;叶绿体数量及内部片层数量变少、体积也明显变小;光合色素(叶绿素a、叶绿素b和类胡萝卜素)含量和叶绿素荧光动力参数(F_o、F_m、F_v/F_m、ФPSⅡ、qP、qN和ETR)均显著降低。‘MT-1’和‘WT-18’的代谢产物差异明显,KEGG代谢通路分析表明,大多数差异代谢物富集到氨基酸代谢、糖代谢、脂类代谢、核酸代谢、次级代谢产物生物合成等途径。因此,叶绿体相关基因的改变可能是发生叶色失绿突变的重要原因。     

重庆地区几种常见单叶与复叶树种叶内生物量分配及异速生长分析

以6种复叶和7种单叶树种为材料,对叶内光合结构和支撑结构的生物量分配及异速生长关系在单叶和复叶树种中的变化规律进行研究.结果显示:单叶树种支撑结构的生物量投资比例显著大于复叶.单叶树种的支撑结构质量比与叶大小(叶面积和总叶干重)无明显的相关性,其光合结构与支撑结构呈等速生长关系;复叶树种的支撑结构质量比随叶大小的增加而...     

Subtype-specific regulation of the expression and function of muscarinic acetylcholine receptors in embryonic chicken retinal cells

We examined the effect of long-term agonist exposure on muscarinic acetylcholine receptor expression and function in embryonic chicken retinal cells. Long-term carbachol exposure induced a time- and concentration-dependent decrease in M2, M3 and M4 muscarinic receptor numbers. Kinetic analyses revealed a first-order process with similar rate constants for all three subtypes. Both the maximal decrease and the agonist potency for regulation of M3 were significantly higher than those for M2 and M4. Upon agonist removal, M2 and M4 numbers returned to control values, but M3 recovery after 24 h was no higher than 40%. Agonist treatment did not alter the levels of receptor mRNAs. Receptor inactivation with a covalent alkylating antagonist demonstrated that the partial M3 protein recovery was not due to a decreased intrinsic basal rate of synthesis, suggesting that it is induced by agonist treatment. Prolonged carbachol exposure induced concomitant decreases in muscarinic-mediated inhibition of cyclic AMP accumulation which were completely reversed after agonist removal. Sustained receptor activation also promoted significant decreases in muscarinic receptor-stimulated phosphoinositide turnover, which were only partially reversed after agonist removal. These data demonstrate subtype-specific regulation of the expression and function of muscarinic receptors in the retina.