a Department of Microbiology, University of Massachusetts, Amherst, Massachusetts 01002
ABSTRACT
Klebsiella aerogenes strain W70 has an inducible pathway for the degradation of D-arabitol which is comparable to the one found in Aerobacter aerogenes strain PRL-R3. The pathway is also similar to the pathway of ribitol catabolism in that it is composed of a pentitol dehydrogenase, D-arabitol dehydrogenase (ADH), and a pentulokinase, D-xylulokinase (DXK). These two enzymes are coordinately controlled and induced in response to D-arabitol, the apparent inducer of synthesis of these enzymes. We obtained mutants which lacked a functional D-xylose pathway and were constitutive for the ribitol catabolic pathway. These mutants were able to grow on the unusual pentitol, xylitol, only if they contained the functional DXK of the D-arabitol pathway. This provided us with a specific selection technique for DXK+ transductants. As in A. aerogenes, mutants constitutive for ADH were able to use this enzyme to convert the hexitol D-mannitol to D-fructose. With mutants blocked in the normal D-mannitol catabolic pathway, growth on D-mannitol became a test for ADH constitutivity. Growth of such mutants on xylitol, D-arabitol, and D-mannitol was utilized to classify transductants in mapping, by transductional analysis, the loci involved in D-arabitol utilization. Three-point crosses gave the order dalK-dalD-dalC, where dalK is the DXK structural gene, dalD is the ADH structural gene, and dalC is a regulatory site controlling synthesis of both enzymes.
1 Present address: Department of Microbiology and Public Health, Michigan State University, East Lansing, Mich. 48823.
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
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| Mol. Cell. Biol. | J. Virol. | Microbiol. Mol. Biol. Rev. |
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