Cross Index | Phototrophic Anoxygenic Bacteria |
SuperSet | Prokaryote, Eubacteria, |
Compare | |
Contrast | Oxygenic Phototrophic Bacteria Archaea |
Subset | Purple Bacteria
Green Bacteria
Anaerobic chemotropic Erythrobacter longus, |
Morphology | Anoxygenic Phototrophic Bacteria |
CELLULAR |
Staining | Gram-negative |
Morphology | Cells are spherical or ovoid or are of short or long rods or spirals of various width; |
Motility | are motile by polar, subpolar or peritrichous flagella or are nonmotile |
Specialized structures | None of the described
species contains gas vacuoles. Internal photosynthetic
membranes are continuous with the cytoplasmic membrane
and consist of fingerlike intrusions, vesicles or
lamellae polysaccharides, poly-B-hydroxybutyric acid and polyphosphate have been found |
Division | and divide by binary fission or show polar growth and budding |
COLONIAL |
Solid surface |
Liquid | Colour of cell suspensions is green, yellowish-green, yellowish-brown, brown, brown-red, red or purple-violet. |
Growth Parameters | Anoxygenic Phototrophic Bacteria |
PHYSIOLOGICAL |
Tropism | Under anaerobic conditions in the light, all species grow as photoheterotrophs with various organic substrates or as photoautotrophs with either molecular hydrogen or, in some species, sulfide, thiosulfate or elemental sulfur as electron donor and CO2 as sole carbon source (growth factors are required in most cases). Under microaerobic to aerobic conditions in the dark, many representatives can grow as chemoheterotrophs, and some grow as chemoautotrophs. |
Oxygen | In most species, the
formation of pigments and of the internal membrane
systems are repressed under aerobic conditions but become
derepressed at oxygen tensions below a certain level. Some species may metabolize anaerobically in the dark with sugars and either nitrate, DMSO or trimethylamine-N-oxide as electron sink or, though poorly, with metabolic intermediates as electron acceptors. Some representatives are very sensitive to oxygen; others grow equally well under aerobic conditions in the dark at the full oxygen tension of air and under anaerobic conditions in the light. |
pH | |
Temperature | |
Requirements | One or more vitamins
are generally required as growth factors; most commonly
required are biotin, thiamine, niacin and p-aminobenzoic
acid. These compounds are rarely needed by species of the
Chromatiaceae and Ectothiorhodospiraceae, which may
require vitamin B12 as sole growth factor. Growth of most
species is enhanced by small amounts of yeast extract,
and some species have a complex nutrient requirement. Ammonia, dinitrogen and several organic nitrogen compounds are generally used as nitrogen source, nitrate is also used by some strains The majority of the species are able to assimilate sulfate as sole sulfur source; only a few species depend on the presence of reduced sulfur compounds as sulfur source. Sulfide is inhibitory for many species already at low concentrations; some, however, exhibit a remarkable tolerance towards this compound |
Products | |
Enzymes | |
Unique features | Photosynthetic pigments are located in the cytoplasmic membrane and the internal membrane systems and are bacteriochlorophyll a or b (esterified with phytol or geranylgeraniol) and various types of carotenoids.. |
ENVIRONMENTAL |
Habitat | Members of this group are widely distributed in nature and found not only in fresh-water, marine and hypersaline environments but also in moist soils and paddy fields. They live preferably in aquatic habitats with significant amounts of soluble organic matter and low oxygen tension, but they rarely form coloured blooms, which are characteristically formed by representative of other families of anoxygenic phototrophic bacteria |
Lifestyle | |
Pathogenicity |
Distribution |
Genome | Anoxygenic Phototrophic Bacteria |
G+C Mol % | 52.0-73.2 (Bd and Tm). |
Reference | Anoxygenic Phototrophic Bacteria |
The Prokaryotes | p |
Bergey's Systematatic | p |
Bergey's Determinative | p 353-376 |
References |