Isolation and Characterization of a Mutant Defective in the Production of Methanol Dehydrogenase from a New Restricted Facultative Methanol‐Oxidizing Bacterium

A new restricted facultative methanol‐oxidizing bacterium Methylobacillus sp. strain SK1 (DSM 8269) was subjected to insertion mutagenesis studies with the transposon Tn5 to generate mutants deficient in the production of methanol dehydrogenase (MDH).The transposon was conjugally transferred into the methylotroph by using the triparental mating procedure. The mutants induced by Tn5 were selected directly from a plate containing succinate by using the allyl alcohol selection procedure. The transposition of Tn5 to the bacterium showed a moderate transposition frequency (10‐5‐10‐6).Southern hybridization analysis confirmed that the transposon Tn5 was inserted into the chromosomal DNA of the mutants. In addition, the mutants had no RNA transcripts produced from the mdh gene, as judged by Northern blot analysis. The mutants could neither grow on methanol nor produce MDH protein, as determined by Western blotanalysis with anti‐MDH antibody. These results suggest that Tn5 mutagenesis maybe a useful tool for the molecular analysis of a facultative methanol‐oxidizing bacterium.

[1]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[2]  J. Murrell,et al.  The methanol dehydrogenase structural gene mxaF and its use as a functional gene probe for methanotrophs and methylotrophs , 1997, Applied and environmental microbiology.

[3]  M. Lidstrom,et al.  Methanol oxidation mutants in Methylobacterium extorquens AM1: identification of new genetic complementation groups. , 1995, Microbiology.

[4]  J. Leigh,et al.  Genetics in methanogens: transposon insertion mutagenesis of a Methanococcus maripaludis nifH gene , 1995, Journal of bacteriology.

[5]  M. Lidstrom,et al.  Isolation, phenotypic characterization, and complementation analysis of mutants of Methylobacterium extorquens AM1 unable to synthesize pyrroloquinoline quinone and sequences of pqqD, pqqG, and pqqC , 1994, Journal of bacteriology.

[6]  R. Aubin,et al.  Simplified high throughput protocol for northern hybridization. , 1993, Nucleic acids research.

[7]  Young Tae Ro,et al.  Methanol Dehydrogenase of an Obligate Methanolotroph, Methylobacillus sp. Strain SK1 , 1991, Molecules and Cells.

[8]  N. Govorukhina,et al.  Methylomicrobium: a new genus of facultative methylotrophic bacteria , 1989 .

[9]  H. Towbin,et al.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[10]  D. Helinski,et al.  Replication of an origin-containing derivative of plasmid RK2 dependent on a plasmid function provided in trans. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[11]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[12]  C. Anthony,et al.  The microbial oxidation of methanol. The alcohol dehydrogenase of Pseudomonas sp. M27. , 1965, The Biochemical journal.

[13]  J. Marmur A procedure for the isolation of deoxyribonucleic acid from micro-organisms , 1961 .

[14]  H. Cheong,et al.  Transposon Tn5 Mutagenesis in Acetobacter sp. HA , 1994 .

[15]  K. Schleifer,et al.  The aerobic methylotrophic bacteria. , 1992 .

[16]  Kim,et al.  A Methylobacillus Isolate Growing Only on Methanol , 1991 .

[17]  M. Lidstrom,et al.  Methylotrophs: genetics and commercial applications. , 1990, Annual review of microbiology.

[18]  C. Anthony Bacterial oxidation of methane and methanol. , 1986, Advances in microbial physiology.