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Encapsulation-Induced Stress Helps Saccharomyces cerevisiae Resist Convertible Lignocellulose Derived Inhibitors
University of Borås, School of Engineering. (Biotechnology)
University of Borås, School of Engineering. (Biotechnology)ORCID iD: 0000-0003-4887-2433
2012 (English)In: International Journal of Molecular Sciences, ISSN 1661-6596, E-ISSN 1422-0067, Vol. 13, no 9, p. 11881-11894Article in journal (Refereed) Published
Sustainable development
The content falls within the scope of Sustainable Development
Abstract [en]

The ability of macroencapsulated Saccharomyces cerevisiae CBS8066 to withstand readily and not readily in situ convertible lignocellulose-derived inhibitors was investigated in anaerobic batch cultivations. It was shown that encapsulation increased the tolerance against readily convertible furan aldehyde inhibitors and to dilute acid spruce hydrolysate, but not to organic acid inhibitors that cannot be metabolized anaerobically. Gene expression analysis showed that the protective effect arising from the encapsulation is evident also on the transcriptome level, as the expression of the stress-related genes YAP1, ATR1 and FLR1 was induced upon encapsulation. The transcript levels were increased due to encapsulation already in the medium without added inhibitors, indicating that the cells sensed low stress level arising from the encapsulation itself. We present a model, where the stress response is induced by nutrient limitation, that this helps the cells to cope with the increased stress added by a toxic medium, and that superficial cells in the capsules degrade convertible inhibitors, alleviating the inhibition for the cells deeper in the capsule.

Place, publisher, year, edition, pages
MDPI , 2012. Vol. 13, no 9, p. 11881-11894
Keywords [en]
lignocellulosic hydrolysate, ethanol, furfural, HMF (5-hydroxymethyl furfural), carboxylic acids, encapsulation, Saccharomyces cerevisiae, biofuel, inhibitors, q-PCR, Resource Recovery
National Category
Other Industrial Biotechnology
Research subject
Resource Recovery
Identifiers
URN: urn:nbn:se:hb:diva-1319DOI: 10.3390/ijms130911881ISI: 000309272700075PubMedID: 23109889Local ID: 2320/11425OAI: oai:DiVA.org:hb-1319DiVA, id: diva2:869343
Available from: 2015-11-13 Created: 2015-11-13 Last updated: 2022-02-10

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Westman, Johan O.Taherzadeh, Mohammad J

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