Pleotropic mutants from Alcaligenes eutrophus defective in the metabolism of hydrogen,nitrate, urea,and fumarate |
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Authors: | D. Römermann M. Lohmeyer C. G. Friedrich B. Friedrich |
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Affiliation: | (1) Institut für Pflanzenphysiologie Zellbiologie und Mikrobiologie der Freien Universität Berlin, Königin-Luise-Strasse 12-16, D-1000 Berlin 33;(2) Institut für Mikrobiologie der Universität Göttingen, Grisebachstrasse 8, D-3400 Göttingen, Federal Republic of Germany;(3) Fachbereich Chemie und Biotechnik, Technische Fachhochschule Berlin, Luxemburger Strasse 10, D-1000 Berlin 65 |
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Abstract: | Chromosomal mutants of Alcaligenes eutrophus unable to grow with molecular hydrogen as the energy source also failed to grow with nitrate as the terminal electron acceptor or as a nitrogen source. The mutants (Hno–) (i) formed neither soluble nor particulate hydrogenase antigens, (ii) expressed only about 50% the wild type level of ribulosebisphosphate carboxylase activity, and (iii) transported nickel, an essential constituent of active hydrogenase, at a significantly lower rate than wild type cells. Moreover, the mutants grew very slowly with urea as nitrogen source and did not express urease. Growth on formamide was also affected and formamidase activity was induced to only a very low level. Growth of the Hno– mutants on succinate, glutamate, fumarate, and malate was significantly slower than wild type, and a reduced rate of succinate incorporation into the mutant cells was demonstrated. The highly pleiotropic phenotype of Hno– mutants is indicative of a chromosomal gene with a considerable physiological importance. It affected the expression of both chromosomal and megaplasmid encoded systems of energy, carbon, and nitrogen metabolism. Thus, the hno mutation restricts the metabolic versatility but does not affect the basic metabolic functions of the organism. |
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Keywords: | Pleiotropic mutants Alcaligenes eutrophus Hydrogenase Ribulosebisphosphate carboxylase Transport Urease Formamidase |
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