1960
DOI: 10.1016/0006-3002(60)90045-7
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The chlorophylls of green bacteria

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1964
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Cited by 175 publications
(71 citation statements)
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“…Heme-positive cytochrome c-550.5 is found in both zones, in discrete concentration peaks. The spectra of the brownish zone in fig.2 show that only a small amount of BChl c (or bacteriopheophytin [25]) and about 0.25 cytochrome c-550.5 per cytochrome b-562 are present (assuming E = 20 mM_' *cm-' at the a-peaks). Redox titrations, performed at pH 6.2 as in [26], COOMASSIE HEME kD I 6%…”
Section: Resultsmentioning
confidence: 99%
“…Heme-positive cytochrome c-550.5 is found in both zones, in discrete concentration peaks. The spectra of the brownish zone in fig.2 show that only a small amount of BChl c (or bacteriopheophytin [25]) and about 0.25 cytochrome c-550.5 per cytochrome b-562 are present (assuming E = 20 mM_' *cm-' at the a-peaks). Redox titrations, performed at pH 6.2 as in [26], COOMASSIE HEME kD I 6%…”
Section: Resultsmentioning
confidence: 99%
“…If compound 2 is 2-devinyl-2-hydroxyethylphaeophorbid a, dehydration of the hydroxylated (Stanier & Smith, 1960) Amax. side chain should yield phaeophorbid a.…”
Section: Resultsmentioning
confidence: 99%
“…One of the pigments (compound 2 of Jones, 1963 b), which was isolated from the inhibited cells and medium, corresponds very closely in spectroscopic properties with the magnesium-free derivative of Chlorobium chlorophyll (650), the photosynthetic pigment of certain bacteria (Stanier & Smith, 1960). Compound 2 differs from Chlorobium phaeophorbid (650) in that it gives a positive reaction in the Molisch phase test for the presence of an isocyclic ring substituted with a carboxylic group, a reaction given by chlorophyll a, bacteriochlorophyll and the magnesium-free derivatives of these compounds (phaeophytins).…”
mentioning
confidence: 95%
“…To remove traces of ascorbate, the pellet was washed with 500 ml Na 2 HPO 4 /NaH 2 PO 4 (20 mM, pH 7.0) and stored at 280 uC until the measurements were performed. Elemental sulfur, BChl c and BChl d were extracted by resuspending the cell pellet in methanol, and the concentrations were determined spectrophotometrically in the supernatant at 265, 669 and 659 nm, respectively, using absorption coefficients of 23.9 l g 21 cm 21 (Stal et al, 1984), 86 l g 21 cm 21 and 82.3 l g 21 cm 21 (Stanier & Smith, 1960). The A 265 was corrected for pigment contribution by subtracting 40 % of the A 669 and A 659 , respectively (this percentage was empirically determined with sulfur globule-free wild-type cells).…”
Section: Methodsmentioning
confidence: 99%