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D C Brune

Publications and source records attributed to D C Brune.

26 records · Page 2Linked to original sources

Antenna organization in green photosynthetic bacteria. 2. Excitation transfer in detached and membrane-bound chlorosomes from Chloroflexus aurantiacus.

The photosynthetic antenna of Chloroflexus aurantiacus includes bacteriochlorophyll (BChl) C740 and BChl a792, both of which occur in chlorosomes, and B808-866 (containing BChl a808 and BChl a866), which is membrane-located (subscripts refer to near-infrared absorption maxima in vivo). BChl a792 is thought to mediate excitation transfer from BChl c740 to BChl a808. Lifetimes of fluorescence from BChl c740 and BChl a792 were measured in isolated and membrane-bound chlorosomes in order to study energy transfer from these pigments. In both preparations, the lifetime of BChl c740 fluorescence was at or below the instrumental limit of temporal resolution (about 30-50 ps), implying extremely fast excitation transfer from this pigment. Attempts to disrupt excitation transfer from BChl c740, either by conversion of part of this pigment to a monomeric form absorbing at 671 nm or by partial destruction of BChl a792 by oxidation with K3Fe(CN)6, had no discernible effects on the lifetime of BChl c740 fluorescence. Most (usually greater than 90%) of the fluorescence from BChl a792 decayed with a lifetime of 93 +/- 21 ps in membrane-attached chlorosomes and 155 +/- 22 ps in isolated chlorosomes at room temperature. Assuming that the only difference between these preparations is the occurrence of excitation transfer from BChl a792 to B808-866, a 41% efficiency was calculated for this process. This value is lower than the 60% efficiency of excitation transfer from BChl c740 to B808-866 determined by comparison of fluorescence excitation and absorption spectra of membranes with attached chlorosomes and compares even less favorably with the 100% efficiency of excitation transfer found in whole cells by the same method.(ABSTRACT TRUNCATED AT 250 WORDS)

Bacteria↗

Inhibition of photosynthetic sulfide oxidation by organic cations.

Photosynthetic sulfide oxidation by the purple sulfur bacterium Chromatium vinosum is strongly inhibited by the organic cations benzyl viologen ( BV2 +) and tetraphenylphosphonium (TPP+) at micromolar concentrations. Both are much more inhibitory at pH 8 than at pH 7. Inhibition probably results from uptake of benzyl viologen and tetraphenylphosphonium in response to an electrical potential gradient across the plasma membrane which increases in magnitude with increasing pH. Although both compounds appear to have the same mode of action, the biochemical mechanism of their inhibition remains to be determined.

Benzyl Viologen↗

Primary charge separation in bacterial photosynthesis: oxidized chlorophylls and reduced pheophytin.

Bacteriopheophytin, the magnesium-free base of bacteriochlorophyll, undergoes reversible one-electron reduction in organic solvents to yield an anionic free radical with characteristic optical and electron spin resonance spectra. The reduction potential of bacteriopheophytin, E1/2 approximately --0.55 V against a normal hydrogen electrode, compared to E1/2 approximately --0.85 V for bacteriochlorophyll, renders it a likely electron acceptor in the primary charge separation of photosynthesis. Comparison of these data with picosecond optical changes recently observed upon pulsed laser excitation of bacterial reaction centers leads us to propose that bacteriopheophytin is indeed a transient electron acceptor and that the primary charge separation of bacterial photosynthesis occurs between the bacteriochlorophyll complex P870 and bacteriopheophytin to yield the radicals of the oxidized chlorophyll dimer cation and reduced pheophytin anion.

Bacteriochlorophylls↗