Abstract:The succinoxidase system of Aspergillzrs niger differs from that of avian and mammalian tissues in its greater lability during preparation and storage but is similar in its sensitivity to malonate, cyanide, azide, and B.A.L., its association with cell particles, and its single pH optimum a t pH 7.3. T h e system is not inhibited by arsenite in concentrations up to 0.01 M.
MethodsAspergillus niger, N.R.C. 233, was grown in 200 ml. lots of a medium containing 3% malt extract, 0.5Yo yeast extract, and ly0 glucose… Show more
“…It was essentially that used by Martin (1954) and consisted of 1 yo glucose, 8% malt extract, and 0.5% yeast extract dispensed in 100 ml. volumes in 500 ml.…”
Section: Cultures On Jluid Media Glucose Malt-extract Yeast Medium ( mentioning
SUMMARYAconitase and NAD-and NADP-linked isocitric dehydrogenases were examined in two strains of Aspergillus niger. The mutant strain 72-44 produced higher yields of citric acid on the culture medium used than did the parent strain 7 2 4 . After growth for 22 hr on a medium in which citric acid did not accumulate, the amounts of each enzyme in the parent strain were approximately the same as those in the mutant strain. The enzymes were also found, though in lower amounts, throughout the incubation period of 8 days in both strains grown on a medium in which citric acid accumulated. A 20-fold increase in the concentration of iron in this medium doubled the activity of aconitase in extracts from the mutant strain, though citric acid accumulation was only decreased by 25 %. The addition of monofluoroacetate to the culture medium was toxic to the mould and did not stimulate citric acid yields. It is suggested that during the incubation, some recycling of citric acid may take place. The difference in citric acid yields from the parent and mutant strains was not accounted for on the basis of the degrees of aconitase or isocitric dehydrogenase activity.
“…It was essentially that used by Martin (1954) and consisted of 1 yo glucose, 8% malt extract, and 0.5% yeast extract dispensed in 100 ml. volumes in 500 ml.…”
Section: Cultures On Jluid Media Glucose Malt-extract Yeast Medium ( mentioning
SUMMARYAconitase and NAD-and NADP-linked isocitric dehydrogenases were examined in two strains of Aspergillus niger. The mutant strain 72-44 produced higher yields of citric acid on the culture medium used than did the parent strain 7 2 4 . After growth for 22 hr on a medium in which citric acid did not accumulate, the amounts of each enzyme in the parent strain were approximately the same as those in the mutant strain. The enzymes were also found, though in lower amounts, throughout the incubation period of 8 days in both strains grown on a medium in which citric acid accumulated. A 20-fold increase in the concentration of iron in this medium doubled the activity of aconitase in extracts from the mutant strain, though citric acid accumulation was only decreased by 25 %. The addition of monofluoroacetate to the culture medium was toxic to the mould and did not stimulate citric acid yields. It is suggested that during the incubation, some recycling of citric acid may take place. The difference in citric acid yields from the parent and mutant strains was not accounted for on the basis of the degrees of aconitase or isocitric dehydrogenase activity.
“…It has been shown that the TCA cycle is operative during the growth of cultures of A. niger (Ramakrishnan, 1954;Ramakrishnan and Martin, 1954;Yeoman, i960). Martin (1954) detected a conventional succinoxidase system in this fungus. The conclusion that such a system is operating in the cellular oxidation of sugars and other normal metabolites in this fungus was strengthened by the detection in Experiments C and D of labelled cyclic acids after feeding mycelia with radioactive malonate.…”
SUMMARYThe effects of malonate on the gaseous exchange and acid metabolism of mycelial suspensions of Aspergillus tiiger have been studied.Malonate penetrated into the cells of the fungus but did not exert its normal effect as a competitive inhibitor in the TCA cycle, even at high external concentrations. On the contrary it stimulated oxidative catabohsm. Some of the malonate which penetrated was consumed by the fungus and it is inferred that the remainder was stored within the mycelium away from malonate sensitive centres in the cytoplasm.Experiments performed with [2-i'*C] malonate have shown that part of the malonate molecule may be utilized in the synthesis of larger structural molecules of the mycelium. Possible pathways of malonate metabolism are discussed in the light of work carried out with other organisms.
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