Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/58798
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dc.contributor.authorSchaller, Andreaen
dc.contributor.authorConnors, Natalie Ken
dc.contributor.authorDimitrijev Dwyer, Mirjanaen
dc.contributor.authorOelmeier, Stefan Aen
dc.contributor.authorHubbuch, Jurgenen
dc.contributor.authorMiddelberg, Anton P Jen
dc.date.accessioned2024-04-30T06:53:45Z-
dc.date.available2024-04-30T06:53:45Z-
dc.date.issued2015-
dc.identifier.citationJournal of Computer-Aided Molecular Design, v.29, p. 47-58en
dc.identifier.issn1573-4951en
dc.identifier.issn0920-654Xen
dc.identifier.urihttps://hdl.handle.net/1959.11/58798-
dc.description.abstract<p>Biosurfactants are surface-active molecules produced principally by microorganisms. They are a sustainable alternative to chemically-synthesized surfactants, having the advantages of being non-toxic, highly functional, eco-friendly and biodegradable. However they are currently only used in a few industrial products due to costs associated with production and purification, which exceed those for commodity chemical surfactants. DAMP4, a member of a four-helix bundle biosurfactant protein family, can be produced in soluble form and at high yield in Escherichia coli, and can be recovered using a facile thermal phase-separation approach. As such, it encompasses an interesting synergy of biomolecular and chemical engineering with prospects for low-cost production even for industrial sectors. DAMP4 is highly functional, and due to its extraordinary thermal stability it can be purified in a simple two-step process, in which the combination of high temperature and salt leads to denaturation of all contaminants, whereas DAMP4 stays stable in solution and can be recovered by filtration. This study aimed to characterize and understand the fundamental drivers of DAMP4 stability to guide further process and surfactant design studies. The complementary use of experiments and molecular dynamics simulation revealed a broad pH and temperature tolerance for DAMP4, with a melting point of 122.4 °C, suggesting the hydrophobic core as the major contributor to thermal stability. Simulation of systematically created in silico variants of DAMP4 showed an influence of number and location of hydrophilic mutations in the hydrophobic core on stability, demonstrating a tolerance of up to three mutations before a strong loss in stability occurred. The results suggest a consideration of a balance of stability, functionality and kinetics for new designs according to their application, aiming for maximal functionality but at adequate stability to allow for cost-efficient production using thermal phase separation approaches.</p>en
dc.languageenen
dc.publisherSpringer Dordrechten
dc.relation.ispartofJournal of Computer-Aided Molecular Designen
dc.titleComputational study of elements of stability of a four-helix bundle protein biosurfactanten
dc.typeJournal Articleen
dc.identifier.doi10.1007/s10822-014-9803-6en
local.contributor.firstnameAndreaen
local.contributor.firstnameNatalie Ken
local.contributor.firstnameMirjanaen
local.contributor.firstnameStefan Aen
local.contributor.firstnameJurgenen
local.contributor.firstnameAnton P Jen
local.relation.isfundedbyARCen
local.profile.schoolAnimal Genetics and Breeding Uniten
local.profile.emailnconnor2@une.edu.auen
local.output.categoryC1en
local.grant.numberDP120103683en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.publisher.placeThe Netherlandsen
local.format.startpage47en
local.format.endpage58en
local.peerreviewedYesen
local.identifier.volume29en
local.contributor.lastnameSchalleren
local.contributor.lastnameConnorsen
local.contributor.lastnameDimitrijev Dwyeren
local.contributor.lastnameOelmeieren
local.contributor.lastnameHubbuchen
local.contributor.lastnameMiddelbergen
dc.identifier.staffune-id:nconnor2en
local.profile.orcid0000-0003-4866-4757en
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:1959.11/58798en
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
local.title.maintitleComputational study of elements of stability of a four-helix bundle protein biosurfactanten
local.relation.fundingsourcenoteA.S. was financially supported by an UQI Tuition Fee Scholarship and an AIBN RHD Living Scholarship. A.P.J.M. thanks the Queensland Government award of the 2010 Smart State Premier's Fellowship.en
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.relation.grantdescriptionARC/DP120103683en
local.search.authorSchaller, Andreaen
local.search.authorConnors, Natalie Ken
local.search.authorDimitrijev Dwyer, Mirjanaen
local.search.authorOelmeier, Stefan Aen
local.search.authorHubbuch, Jurgenen
local.search.authorMiddelberg, Anton P Jen
local.uneassociationNoen
local.atsiresearchNoen
local.sensitive.culturalNoen
local.year.published2015en
local.fileurl.closedpublishedhttps://rune.une.edu.au/web/retrieve/999ca548-fdb0-4662-bd97-4a6f21918fc7en
local.subject.for20203003 Animal productionen
local.subject.seo2020TBDen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.date.moved2024-04-30en
Appears in Collections:Animal Genetics and Breeding Unit (AGBU)
Journal Article
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