Tricarboxylic acid and glyoxylate cycle enzyme activities in Thiobacillus versutus, an isocitrate lyase negative organism View Full Text


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Article Info

DATE

1986-07

AUTHORS

Pieternel A. M. Claassen, Gerard J. J. Kortstee, Johannes P. van Dijken, Wim Harder

ABSTRACT

An analysis was made of the specific enzyme activities of the TCA and glyoxylate cycle in Thiobacillus versutus cells grown in a thiosulphate- or acetate-limited chemostat. Activities of all enzymes of the TCA cycle were detected, irrespective of the growth substrate and they were invariably lower in the thiosulphate-grown cells. Of the glyoxylate cycle enzymes, isocitrate lyase was absent but malate synthase activity was increased from 15 nmol·min-1·mg-1 protein in thiosulphate-grown cells to 58 nmol·min-1·mg-1 protein in acetate-grown cells. Suspensions of cells grown on thiosulphate were able to oxidize acetate, although the rate was 3 times lower than that observed with acetate-grown cells. The respiration of acetate was completely inhibited by 10 mM fluoroacetate or 5 mM arsenite. Partially purified citrate synthase from both thiosulphate- and acetate-grown cells was completely inhibited by 0.5 mM NADH and was insensitive to inhibition by 1 mM 2-oxoglutarate or 1 mM ATP. The specific enzyme activities of the TCA and glyoxylate cycle in T. versutus were compared with those of Pseudomonas fluorescens, an isocitrate lyase positive organism, after growth in a chemostat limited by acetate, glutarate, succinate or glutamate. The response of the various enzyme activities to a change in substrate was similar in both organisms, with the exception of isocitrate lyase. More... »

PAGES

148-152

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00446772

DOI

http://dx.doi.org/10.1007/bf00446772

DIMENSIONS

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