2007
DOI: 10.1007/s00253-007-1132-4
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Membrane-bound l- and d-lactate dehydrogenase activities of a newly isolated Pseudomonas stutzeri strain

Abstract: Pseudomonas stutzeri SDM was newly isolated from soil, and two stereospecific NAD-independent lactate dehydrogenase (iLDH) activities were detected in membrane of the cells cultured in a medium containing DL-lactate as the sole carbon source. Neither enzyme activities was constitutive, but both of them might be induced by either enantiomer of lactate. P. stutzeri SDM preferred to utilize lactate to growth, when both L-lactate and glucose were available, and the consumption of glucose was observed only after la… Show more

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Cited by 49 publications
(52 citation statements)
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“…Unlike the situation in E. coli and C. glutamicum, D-iLDH and L-iLDH are induced coordinately in these Pseudomonas strains (12,21,22). Neither of the enzymes is constitutively expressed, and either enantiomer of lactate can induce the expression of both enzymes (12,21,22). These results indicate that the iLDH regulatory mechanism in Pseudomonas strains may be different from the wellstudied mechanism in E. coli and C. glutamicum.…”
contrasting
confidence: 41%
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“…Unlike the situation in E. coli and C. glutamicum, D-iLDH and L-iLDH are induced coordinately in these Pseudomonas strains (12,21,22). Neither of the enzymes is constitutively expressed, and either enantiomer of lactate can induce the expression of both enzymes (12,21,22). These results indicate that the iLDH regulatory mechanism in Pseudomonas strains may be different from the wellstudied mechanism in E. coli and C. glutamicum.…”
contrasting
confidence: 41%
“…Unlike the situation in E. coli and C. glutamicum, D-iLDH and L-iLDH are induced coordinately in these Pseudomonas strains (12,21,22). Neither of the enzymes is constitutively expressed, and either enantiomer of lactate can induce the expression of both enzymes (12,21,22).…”
mentioning
confidence: 94%
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