Publication:
Metabolic networks and bioenergetics of Aurantiochytrium sp. B-072 during storage lipid formation

dc.contributor.authorMontri Chaisawangen_US
dc.contributor.authorCornelis Verduynen_US
dc.contributor.authorSomchai Chauvatcharinen_US
dc.contributor.authorManop Suphantharikaen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-11T04:52:43Z
dc.date.available2018-06-11T04:52:43Z
dc.date.issued2012-07-01en_US
dc.description.abstractBaffled shake flask cultivation of Aurantiochytrium sp. B-072 was carried out at in a glucose-monosodium glutamate mineral medium at different C/N-ratios (30-165) with glucose fixed at 90 g/L. With increasing C/N-ratio, a modest increase in lipid content (60 to 73 % w/w) was observed whereas fat-free biomass decreased but overall biomass showed little variation. FA-profiles were not affected to a large extent by C/N-ratio and absolute docosahexaenoic (DHA)-levels fell in narrow range (5-6 g/L). However at C/N > 64 a rapid decrease in lipid synthetic rate and/or incomplete glucose utilization occurred. Glucose and FAfluxes based on fat-free biomass peaked at a C/N ratio of 56. This condition was chosen for calculation of the redox balance (NAD(P)H) and energy (ATP) requirement and to estimate the in vivo P/O ratio during the main period of fatty acid biosynthesis. Several models with different routes for NADPH, acetyl-CoA formation and re-oxidation of OAA formed via ATP-citrate lyase were considered as these influence the redox- and energy balance. As an example, using a commonly shown scheme whereby NADPH is supplied by a cytosolic "transhydrogenase cycle" (pyruvate-OAA-malate-pyruvate) and OAA formed by ATP-citrate lyase is recycled via import into the mitochondria as malate, the calculated NADPH-requirement amounted to 5.5 with an ATP-demand of 10.5 mmol/(g fat-free biomass x h) and an in vivo P/O-ratio (not including non-growth associated maintenance) of 1.6. The lowest ATP requirement is found when acetyl-CoA would be transported directly from the mitochondria to the cytosol by carnitine acetyltransferase. Assay of some enzymes critical for NADPH supply indicates that activity of glucose-6-phosphate dehydrogenase, the first enzyme in the HMP pathway, is far insufficient for the required NADPH-flux and malic enzyme must be a major source. Activity of the latter (ca. 300 mU/mg protein) far exceeds that in oleaginous fungi and yeast.en_US
dc.identifier.citationBrazilian Journal of Microbiology. Vol.43, No.3 (2012), 1192-1205en_US
dc.identifier.doi10.1590/S1517-83822012000300047en_US
dc.identifier.issn16784405en_US
dc.identifier.issn15178382en_US
dc.identifier.other2-s2.0-84870660066en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/14296
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870660066&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titleMetabolic networks and bioenergetics of Aurantiochytrium sp. B-072 during storage lipid formationen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870660066&origin=inwarden_US

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