Uptake of methylamine and methanol by Pseudomonas sp. strain AM1
- 1 June 1983
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 154 (3) , 1168-1173
- https://doi.org/10.1128/jb.154.3.1168-1173.1983
Abstract
The uptake of methylamine and of methanol by the facultative methylotroph Pseudomonas sp. strain AM1 was investigated. It was found that this organism possesses two uptake systems for methylamine. One of these operates when methylamine is the sole source of carbon, nitrogen, and energy. It has a Km of 1.33 X 10(-4) M and a Vmax of 67 nmol/min per mg of cells (dry weight). The other system, found when methylamine is the sole nitrogen source only, has a Km of 1.2 X 10(-5) M and a Vmax of 8.9 nmol/min per mg of cells (dry weight). Both uptake systems were severely inhibited by azide, cyanide, carbonyl cyanide-m-chlorophenyl hydrazone, and N-ethylmaleimide, but only the high-affinity system was inhibited by ammonium ions with a Ki of 7.7 mM. Both systems were susceptible to osmotic shock treatment, competitively inhibited by ethylamine, and unaffected by most amino acids. Methanol uptake showed a Km of 4.8 microM and a Vmax of 60.6 nmol/min per mg of cells (dry weight) and was not inhibited by osmotic shock treatment. Azide, cyanide, and N-ethylmaleimide curtailed uptake, but carbonyl cyanide-m-chlorophenyl hydrazone merely reduced the rate of uptake. A methanol dehydrogenase mutant, M15A, was unable to take up methanol. It is proposed that methanol diffuses into the cell where it is rapidly oxidized by methanol dehydrogenase.This publication has 21 references indexed in Scilit:
- A periplasmic location for methanol dehydrogenase from : Implications for proton pumping by cytochrome aa3Biochemical and Biophysical Research Communications, 1981
- The dye-linked alcohol dehydrogenase of Rhodopseudomonas acidophila. Comparison with dye-linked methanol dehydrogenasesBiochemical Journal, 1978
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976
- Methylamine metabolism in a pseudomonas speciesArchives of Biochemistry and Biophysics, 1972
- Microbial metabolism of C1 and C2 compounds. The involvement of glycollate in the metabolism of ethanol and of acetate by Pseudomonas AM1Biochemical Journal, 1972
- An N-methyl glutamate dehydrogenase from Pseudomonas M.AArchives of Biochemistry and Biophysics, 1971
- Purification and properties of an amine dehydrogenase from Pseudomonas AM1 and its role in growth on methylamineBiochemical Journal, 1968
- Microbial growth on C1 compounds. 3. Distribution of radioactivity in metabolites of methanol-grown Pseudomonas AM1 after incubation with [14C]methanol and [14C]bicarbonateBiochemical Journal, 1962
- Microbial growth on C1 compounds. 1. Isolation and characterization of Pseudomonas AM 1Biochemical Journal, 1961