Methanolacinia paynteri |
Morphology | Methanolacinia paynteri |
CELLULAR |
Staining | Gram negative |
Morphology | short irregular rods (0.6 um diameter x 1.5-2.5 um long) |
Motility | non motile or very weakly motile, flagella may be present |
Specialized structures | no endospores |
Division |
COLONIAL |
Solid surface |
Liquid |
Growth Parameters | Methanolacinia paynteri |
PHYSIOLOGICAL |
Tropism | |
Oxygen | Very strictly anaerobic |
pH | optimum pH 6.6-7.2 |
Temperature | optimum 40 oC |
Requires | ammmonia may serve as the sole nitrogen source and sulfide may serve as the sulfur source. Acetate is required |
Produces | energy metabolism is by reduction of CO2 to methane with H2 or secondary alcohols as the electron donor. Acetate, formate, methylalmines, methanol and methanol + H2 are not catabolized |
Enzymes | |
Unique features | Cells do not contain
muramic acid. Lipids are predominantly isoprenoid
hydrocarbons ether-linked to glycerol. Cells contain
coenzyme M and coenzyme F420 susceptible to lysis by detergent |
ENVIRONMENTAL |
Habitat | marine sediments |
Lifestyle | |
Pathogenicity |
Distribution |
Genome | Methanolacinia paynteri |
G+C Mol % |
Reference | Methanolacinia paynteri |
First Citation | Zellner et al 1989 J. Gen. Appl Microbiol 35:
185-202 Zellner et al 1990 IJSB 40: 470-471 |
The Prokaryotes | p |
Bergey's Determinative | p 722 |
References |