dc.contributor.author | Vamvakaki, A-N | en |
dc.contributor.author | Kandarakis, I | en |
dc.contributor.author | Kaminarides, S | en |
dc.contributor.author | Komaitis, M | en |
dc.contributor.author | Papanikolaou, S | en |
dc.date.accessioned | 2014-06-06T06:50:06Z | |
dc.date.available | 2014-06-06T06:50:06Z | |
dc.date.issued | 2010 | en |
dc.identifier.issn | 16180240 | en |
dc.identifier.uri | http://dx.doi.org/10.1002/elsc.201000063 | en |
dc.identifier.uri | http://62.217.125.90/xmlui/handle/123456789/4962 | |
dc.subject | γ-linolenic acid | en |
dc.subject | Biomass | en |
dc.subject | Single-cell oil | en |
dc.subject | Whey | en |
dc.subject | Zygomycetes | en |
dc.subject.other | Ammonium Sulfate | en |
dc.subject.other | Biomass productions | en |
dc.subject.other | C/N ratio | en |
dc.subject.other | Cheese whey | en |
dc.subject.other | Elegans | en |
dc.subject.other | Fatty acid composition | en |
dc.subject.other | GLA production | en |
dc.subject.other | Linolenic acids | en |
dc.subject.other | Microbial lipids | en |
dc.subject.other | Molar ratio | en |
dc.subject.other | Mortierella | en |
dc.subject.other | Neutral lipid | en |
dc.subject.other | Single-cell oil | en |
dc.subject.other | Total lipids | en |
dc.subject.other | Whey | en |
dc.subject.other | Zygomycetes | en |
dc.subject.other | Acids | en |
dc.subject.other | Ammonium compounds | en |
dc.subject.other | Biomass | en |
dc.subject.other | Cell culture | en |
dc.subject.other | Fatty acids | en |
dc.subject.other | Fungi | en |
dc.subject.other | Phospholipids | en |
dc.subject.other | Sugars | en |
dc.subject.other | Ecology | en |
dc.subject.other | ammonium sulfate | en |
dc.subject.other | gamma linolenic acid | en |
dc.subject.other | lactose | en |
dc.subject.other | lipid | en |
dc.subject.other | protein | en |
dc.subject.other | biomass | en |
dc.subject.other | cultivation | en |
dc.subject.other | fatty acid | en |
dc.subject.other | fermentation | en |
dc.subject.other | fungus | en |
dc.subject.other | growth rate | en |
dc.subject.other | phospholipid | en |
dc.subject.other | protein | en |
dc.subject.other | substrate | en |
dc.subject.other | article | en |
dc.subject.other | bacterial growth | en |
dc.subject.other | bacterium culture | en |
dc.subject.other | biomass production | en |
dc.subject.other | cheese | en |
dc.subject.other | fatty acid analysis | en |
dc.subject.other | lipid analysis | en |
dc.subject.other | mortierella isabellina | en |
dc.subject.other | Mucor | en |
dc.subject.other | nonhuman | en |
dc.subject.other | Thamnidium elegans | en |
dc.subject.other | whey | en |
dc.subject.other | Zygomycetes | en |
dc.subject.other | Fungi | en |
dc.subject.other | Mucor | en |
dc.subject.other | Thamnidium elegans | en |
dc.subject.other | Umbelopsis isabellina | en |
dc.subject.other | Zygomycetes | en |
dc.title | Cheese whey as a renewable substrate for microbial lipid and biomass production by Zygomycetes | en |
heal.type | journalArticle | en |
heal.identifier.primary | 10.1002/elsc.201000063 | en |
heal.publicationDate | 2010 | en |
heal.abstract | Three Zygomycetes, Mortierella isabellina, Thamnidium elegans and Mucor sp., were tested for their ability of producing biomass and lipid-containing γ-linolenic acid (GLA) during their cultivation on cheese whey. M. isabellina consumed all of the available lactose and a significant amount of the available protein. On the contrary, the two other fungi seemed incapable of consuming lactose after protein exhaustion. In the second series of experiments, for M. isabellina a supplementary quantity of lactose was added into the medium in order to increase the C/N ratio and hence to increase the production of fat. In the case of T. elegans and Mucor sp., a supplementary quantity of ammonium sulfate was added in order to favor the consumption of lactose and the production of biomass. Indeed, enhancement of lipid production was observed for M. isabellina and biomass production for T. elegans and Mucor sp.. Fatty acid analysis of the microbial lipid showed a composition that presented non-negligible changes in relation with the age of the culture and the C/N molar ratio of the medium. Further analysis of the fat showed that the quantity of neutral lipids was the more abundant. The fatty acid composition of neutral lipids resembled to that of total lipids. Phospholipids were the more unsaturated fraction for Mucor sp. and M. isabellina. GLA was synthesized in all trials but its concentration presented differences related with the utilized strains and the fermentation time. Growth of M. isabellina on lactose-supplemented whey resulted in a maximum GLA production of 301 mg/L. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA. | en |
heal.journalName | Engineering in Life Sciences | en |
dc.identifier.issue | 4 | en |
dc.identifier.volume | 10 | en |
dc.identifier.doi | 10.1002/elsc.201000063 | en |
dc.identifier.spage | 348 | en |
dc.identifier.epage | 360 | en |
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