chlorophyll-a and pyridine

Mitochondrial dihydrolipoyl dehydrogenase (mtLPD; L-protein) is an integral component of several multienzyme systems involved in the tricarboxylic acid (TCA) cycle, photorespiration, and the degradation of branched-chain α-ketoacids. The majority of the mtLPD present in photosynthesizing tissue is used for glycine decarboxylase (GDC), necessary for the high-flux photorespiratory glycine-into-serine conversion. We previously suggested that GDC activity could be a signal in a regulatory network that adjusts carbon flux through the Calvin-Benson cycle in response to photorespiration. Here, we show that elevated GDC L-protein activity significantly alters several diagnostic parameters of cellular metabolism and leaf gas exchange in Arabidopsis thaliana. Overexpressor lines displayed markedly decreased steady state contents of TCA cycle and photorespiratory intermediates as well as elevated NAD(P)(+)-to-NAD(P)H ratios. Additionally, increased rates of CO2 assimilation, photorespiration, and plant growth were observed. Intriguingly, however, day respiration rates remained unaffected. By contrast, respiration was enhanced in the first half of the dark phase but depressed in the second. We also observed enhanced sucrose biosynthesis in the light in combination with a lower diel magnitude of starch accumulation and breakdown. These data thus substantiate our prior hypothesis that facilitating flux through the photorespiratory pathway stimulates photosynthetic CO2 assimilation in the Calvin-Benson cycle. They furthermore suggest that this regulation is, at least in part, dependent on increased light-capture/use efficiency.

Topics: Arabidopsis; Biomass; Carbon Isotopes; Cell Respiration; Chlorophyll; Citric Acid Cycle; Dihydrolipoamide Dehydrogenase; Gases; Light; Metabolome; Mitochondria; NADP; Nucleotides; Phenotype; Photosynthesis; Plant Leaves; Plants, Genetically Modified; Pyridines; Ribulose-Bisphosphate Carboxylase; Solubility; Starch; Sulfides

Self-assembled structures formed from a pyridine-appended zinc chlorophyll derivative are reported. While the zinc complex forms cyclic oligomers in chloroform solution, as indicated by (1)H NMR studies (including diffusion-ordered spectroscopy), vapor pressure osmometry, and cold-spray ionization mass spectrometry, it forms double-stranded helical coordination polymers in the solid state, as revealed by single-crystal X-ray analysis.

Topics: Chlorophyll; Coordination Complexes; Models, Molecular; Molecular Structure; Pyridines; Zinc

The mechanism of acetate-assisted transmetalation of tetrapyrroles was investigated in a model system consisting of chlorophyll a and copper(II) acetate in organic solvents by using a spectroscopic and kinetic approach. Surprisingly, acetate ions bind to the central Mg in chlorophyll much more strongly than do acetonitrile, methanol and even pyridine, one of the best ligands in chlorophyllic systems. This exceptionally strong non-symmetrical axial ligation of the central Mg by acetate causes its out-of-plane displacement and deformation of the tetrapyrrole ring, thus facilitating the interaction with an incoming CuII complex. This mechanism is controlled by a keto-enol tautomerism of the chlorophyll isocyclic ring. Additionally, depending on solvent, acetate activates the incoming metal ions. These new insights allow to suggest a mechanism for the acetate method of metal exchange in tetrapyrrolic macrocycles, which resembles biological insertion of metal ions into porphyrins. It also provides a guideline for the design of more efficient methods for the metalation of porphyrins and related macrocycles.

Topics: Acetates; Chlorophyll; Copper; Ethanol; Isomerism; Kinetics; Magnesium; Metals; Nitrogen; Pyridines; Quaternary Ammonium Compounds; Solvents; Spectrophotometry; Tetrapyrroles; Titrimetry

Acaryochloris marina is a unique photosynthetic prokaryote containing chlorophyll(Chl)-d as a major photoactive pigment (over 95%). The molecular structure of Chl-d is proposed as the 3-formyl analog of Chl-a. However, the stereochemistry of Chl-d at the 13(2)-, 17- and 18-positions has not yet been established unambiguously. In the first part of this paper, we describe the determination of their stereochemistries to be 13(2)-(R)-, 17-(S)- and 18-(S)-configurations by using 1H-1H NOE correlations in 1H-NMR and circular dichroism spectra as well as chemical modification of Chl-a to produce stereochemically defined Chl derivatives. In the second part of the paper, we report a facile synthesis of a self-aggregative Chl by modifying isolated Chl-d. Since Chl-d was characterized by its reactive 3-formyl group, the formyl group was reduced with t-BuNH2BH3 to afford the desirable Chl, 3-deformyl-3-hydroxymethyl-pyrochlorophyll-d (3(1)-OH-pyroChl-d). The synthetic 3(1)-OH-pyroChl-d molecules spontaneously self-organized to form well-ordered aggregates in a non-polar organic solvent. The self-aggregates are a good model of major light-harvesting antenna systems of green photosynthetic bacteria, chlorosomes, in terms of the following three findings. (1) Both the red-shifted electronic absorption band above 750 nm and its induced reverse S-shape CD signal around 750 nm were observed in 0.5% (v/v) THF-cyclohexane. (2) The stretching mode of the 13-carbonyl group was downshifted by about 35 cm(-1) from the wavenumber of its free carbonyl. (3) The self-aggregates were quite stable on titration of pyridine to the suspension, in comparison with those of natural chlorosomal bacteriochlorophyll-d possessing the 3-(1-hydroxyethyl) group.

Topics: Bacteriochlorophylls; Chlorobi; Chlorophyll; Chromatography, High Pressure Liquid; Cyanobacteria; Molecular Conformation; Pyridines; Sensitivity and Specificity; Spectrum Analysis; Stereoisomerism; Titrimetry

A monolithic C18-bonded silica rod column (Merck Chromolith) was applied to the separation of mixtures of chlorophylls a and b and their derivatives originated by hydrolysis of the phytyl ester linkage (chlorophyllides), loss of the central Mg atom (pheophytins), or both processes (pheophorbides). Mobile phases containing two different ion-pair reagents, ammonium acetate and buffered pyridine, were tested. Both eluents achieved the resolution of the eight pigments in less than 5 min. The method based on the pyridine-containing mobile phase was applied to the separation of chlorophylls and their green coloured degradation products in senescing leaves of deciduous trees, green fruits and a marine microalga.

Topics: Chlorophyll; Chlorophyll A; Esters; Metals; Phytic Acid; Pyridines; Silicon Dioxide

By dynamic changes in protein structure and function, the photosynthetic membranes of plants are able to regulate the partitioning of absorbed light energy between utilization in photosynthesis and photoprotective non-radiative dissipation of the excess energy. This process is controlled by features of the intact membrane, the transmembrane pH gradient, the organization of the photosystem II antenna proteins and the reversible binding of a specific carotenoid, zeaxanthin. Resonance Raman spectroscopy has been applied for the first time to wild type and mutant Arabidopsis leaves and to intact thylakoid membranes to investigate the nature of the absorption changes obligatorily associated with the energy dissipation process. The observed changes in the carotenoid Resonance Raman spectrum proved that zeaxanthin was involved and indicated a dramatic change in zeaxanthin environment that specifically alters the pigment configuration and red-shifts the absorption spectrum. This activation of zeaxanthin is a key event in the regulation of light harvesting.

Topics: Arabidopsis; beta Carotene; Chlorophyll; Chloroplasts; Hydrogen-Ion Concentration; Light; Lipids; Micelles; Photosynthesis; Protein Conformation; Pyridines; Spectrum Analysis, Raman; Time Factors; Xanthophylls; Zeaxanthins

Zinc chlorins were prepared from chlorophyll-a. Visible spectra in benzene showed that synthetic zinc chlorins complexed with pyridine as an axial ligand to form the monopyridine adducts. The equilibrium constants for the complexation were dependent upon the chlorin structure: substitution of electron-withdrawing groups at the peripheral position enhanced the coordinated ability of the central zinc. 1H NMR spectra in benzene-d6 also indicated that single pyridine coordinated to the central zinc. Comparison of the equilibrium constant in a zinc chlorin with those of the corresponding zinc bacteriochlorin (7,8-dihydrochlorin) and porphyrin (17,18-dedihydrochlorin) led to an increase in the saturation and flexibility of the tetrapyrrole pi-plane ligands making the central zinc more axial-ligated. All the zinc tetrapyrroles in benzene complexed with pyridine to form 5-coordinated (1:1) complexes, not 6-coordinated bisadducts. The observed equilibrium constants were consistent with the energy changes of the complexation calculated from molecular modeling.

Topics: Chlorophyll; Chlorophyll A; Drug Design; Indicators and Reagents; Ligands; Magnetic Resonance Spectroscopy; Molecular Structure; Organometallic Compounds; Pyridines; Pyrroles; Spectrophotometry; Structure-Activity Relationship; Tetrapyrroles; Zinc

Topics: Chlorophyll; Coenzymes; Light; NAD; Pyridines; Solutions