Nomenclature Abstract for Methylobacterium rhodesianum Green et al. 1988 emend. Kato et al. 2008.

2003 ◽  
Author(s):  
Charles Thomas Parker ◽  
Dorothea Taylor ◽  
George M Garrity
1995 ◽  
Vol 39 (1) ◽  
pp. 9-20 ◽  
Author(s):  
Jörg-uwe Ackermann ◽  
Susann Müller ◽  
Andreas Lösche ◽  
Thomas Bley ◽  
wolfgang Babel

1994 ◽  
Vol 161 (3) ◽  
pp. 277-280
Author(s):  
Gisela Mothes ◽  
Wolfgang Babel

1995 ◽  
Vol 41 (13) ◽  
pp. 55-59 ◽  
Author(s):  
Uta Breuer ◽  
Jörg-Uwe Ackermann ◽  
Wolfgang Babel

The pink-pigmented facultatively methylotrophic bacterium Methylobacterium rhodesianum MB 126 is able to grow on methanol as the sole source of carbon and energy. Under certain conditions, e.g., limitation of ammonium, phosphate, or oxygen, carbon from methanol is channeled into poly(3-hydroxybutyric acid) (PHB) whereas other polymers or metabolites are hardly overproduced. A mutant of this strain, which we isolated after chemical mutagenesis, is impaired in its ability to synthesize PHB. Under the conditions mentioned above, the mutant still accumulated PHB, but in the absence of ammonium it simultaneously synthesized PHB and a considerable amount of an exopolysaccharide. This phenomenon was surprising insofar as the wild type did not produce exopolysaccharide in such amounts. An attempt was made to elucidate and discuss the possible reasons for these findings.Key words: methylotrophy, serine pathway bacteria, PHB, exopolysaccharides.


1994 ◽  
Vol 161 (3) ◽  
pp. 277-280
Author(s):  
Gisela Mothes ◽  
Wolfgang Babel

2010 ◽  
Vol 76 (16) ◽  
pp. 5585-5591 ◽  
Author(s):  
Tina Hölscher ◽  
Uta Breuer ◽  
Lorenz Adrian ◽  
Hauke Harms ◽  
Thomas Maskow

ABSTRACT In this study, a methylotrophic bacterium, Methylobacterium rhodesianum MB 126, was used for the production of the chiral compound (R)-3-hydroxybutyrate (R-3HB) from methanol. R-3HB is formed during intracellular degradation of the storage polymer (R)-3-polyhydroxybutyrate (PHB). Since the monomer R-3HB does not accumulate under natural conditions, M. rhodesianum was genetically modified. The gene (hbd) encoding the R-3HB-degrading enzyme, R-3HB dehydrogenase, was inactivated in M. rhodesianum. The resulting hbd mutant still exhibited low growth rates on R-3HB as the sole source of carbon and energy, indicating the presence of alternative pathways for R-3HB utilization. Therefore, transposon mutagenesis was carried out with the hbd mutant, and a double mutant unable to grow on R-3HB was obtained. This mutant was shown to be defective in lipoic acid synthase (LipA), resulting in an incomplete citric acid cycle. Using the hbd lipA mutant, we produced 3.2 to 3.5 mM R-3HB in batch and 27 mM (2,800 mg liter−1) in fed-batch cultures. This was achieved by sequences of cultivation conditions initially favoring growth, then PHB accumulation, and finally PHB degradation.


1995 ◽  
Vol 41 (13) ◽  
pp. 124-130 ◽  
Author(s):  
C. G. Föllner ◽  
W. Babel ◽  
A. Steinbüchel

The poly(3-hydroxybutyric acid) (PHB) granules from eight methylotrophic bacteria that use the serine pathway were isolated in a sucrose gradient (1–2 M); these bacteria included members of the genus Methylobacterium, Mycoplana rubra, and PHB-leaky mutants of Methylobacterium rhodesianum. As shown by sodium dodecyl sulfate – polyacrylamide gel electrophoresis, the granules from all investigated methylotrophic strains revealed two major bands representing small proteins. An efficient purification procedure for these two low molecular weight proteins associated with the PHB granules was developed by solubilization of the proteins with Triton X-114 and affinity chromatography on Procion Blue-H-ERD.Key words: poly(3-hydroxybutyric acid), granule-associated proteins, methylotrophic bacteria.


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