Potential of the enzyme laccase for the synthesis and derivatization of antimicrobial compounds

dc.bibliographicCitation.firstPage107
dc.bibliographicCitation.issue4
dc.bibliographicCitation.journalTitleWorld Journal of Microbiology and Biotechnologyeng
dc.bibliographicCitation.volume39
dc.contributor.authorHahn, Veronika
dc.date.accessioned2023-05-22T07:20:00Z
dc.date.available2023-05-22T07:20:00Z
dc.date.issued2023
dc.description.abstractLaccases [E.C. 1.10.3.2, benzenediol:dioxygen oxidoreductase] can oxidize phenolic substances, e.g. di- and polyphenols, hydroxylated biaryls, aminophenols or aryldiamines. This large substrate spectrum is the basis for various reaction possibilities, which include depolymerization and polymerization reactions, but also the coupling of different substance classes. To catalyze these reactions, laccases demand only atmospheric oxygen and no depletive cofactors. The utilization of mild and environmentally friendly reaction conditions such as room temperature, atmospheric pressure, and the avoidance of organic solvents makes the laccase-mediated reaction a valuable tool in green chemistry for the synthesis of biologically active compounds such as antimicrobial substances. In particular, the production of novel antibiotics becomes vital due to the evolution of antibiotic resistances amongst bacteria and fungi. Therefore, laccase-mediated homo- and heteromolecular coupling reactions result in derivatized or newly synthesized antibiotics. The coupling or derivatization of biologically active compounds or its basic structures may allow the development of novel pharmaceuticals, as well as the improvement of efficacy or tolerability of an already applied drug. Furthermore, by the laccase-mediated coupling of two different active substances a synergistic effect may be possible. However, the coupling of compounds that have no described efficacy can lead to biologically active substances by means of laccase. The review summarizes laccase-mediated reactions for the synthesis of antimicrobial compounds valuable for medical purposes. In particular, reactions with two different reaction partners were shown in detail. In addition, studies with in vitro and in vivo experimental data for the confirmation of the antibacterial and/or antifungal efficacy of the products, synthesized with laccase, were of special interest. Analyses of the structure–activity relationship confirm the great potential of the novel compounds. These substances may represent not only a value for pharmaceutical and chemical industry, but also for other industries due to a possible functionalization of surfaces such as wood or textiles.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/12141
dc.identifier.urihttp://dx.doi.org/10.34657/11174
dc.language.isoeng
dc.publisherOxford : Oxford Univ. Press
dc.relation.doihttps://doi.org/10.1007/s11274-023-03539-x
dc.relation.essn1573-0972
dc.relation.issn0959-3993
dc.rights.licenseCC BY 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subject.ddc570
dc.subject.otherAntimicrobial compoundseng
dc.subject.otherCross couplingeng
dc.subject.otherCyclizationeng
dc.subject.otherLaccaseeng
dc.subject.otherWhite chemistryeng
dc.titlePotential of the enzyme laccase for the synthesis and derivatization of antimicrobial compoundseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorINP
wgl.subjectBiowissenschaften/Biologieger
wgl.typeZeitschriftenartikelger
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