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dc.contributor.advisorRühl, Martin
dc.contributor.advisorSträßer, Katja
dc.contributor.advisorWegner, Hermann
dc.contributor.advisorSchäberle, Till
dc.contributor.authorKarrer, Dominik
dc.date.accessioned2022-09-19T14:32:13Z
dc.date.available2022-09-19T14:32:13Z
dc.date.issued2022
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/7719
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-7151
dc.description.abstractBased on transcriptomic, volatilomic and metabolomic data of the model organism Cyclocybe aegerita, the endogenous and enzymatic production of the C8-oxylipins oct-2-en-1-ol, octan-1-ol, oct-2-enal, octanal, octan-3-ol, oct-1-en-3-ol, oct-1-en-3-one and octan-3-one via biotransformations with [U-13C]linoleic acid was compared to the developmental state depending gene expression patterns of putative oxylipin-associated enzyme classes like lipoxygenases, dioxygenases, ene-reductases and alcohol dehydrogenases. On closer consideration of these data sets, the C8-oxylipin production seemed to occur cluster-like. While one cluster (ketonic-cycle) consisted of octan-3-ol, oct-1-en-3-one, octan-3-one and oct-1-en-3-ol, which were detected through out all developmental stages, a second cluster (aldehydic-cycle) primarily active at early developmental stages involved oct-2-enal, octanal, oct-2-en-1-ol and octan-1-ol. Studying these clusters revealed that all C8-oxylipins of the aldehydic-cycle and ketonic-cycle can be derived from oct-2-enal and oct-1-en-3-one, respectively. A detailled consideration of the gene expression patterns revealed several enzyme classes putatively involved in the C8-oxylipin biosynthesis. Especially the two genes AAE3 04864 and AAE3 13549 encoding the lox4- and enr1-gene showed great similarities between their strongly increasing transcript counts with maturation. Subsequent recombinant production of CaeLOX4 and CaeEnR1 revealed that CaeLOX4 showed a preference for C18-fatty acids with the highest affinity towards linoleic acid. Analysis of the reaction product revealed that this LOX selectively oxygenated linoleic acid at position 13 to 13-hydroperoxyoctadecadienoic acid (13-HPOD). CaeEnR1 showed high affinities towards the reduction of oct-1-en-3-one and oct-2-enal to their saturated counterparts octan-3-one and octanal, respectively. Due to the strong similarities between the expression patterns of CaeLOX4 and CaeEnR1 a coherence between their main reaction products 13-HPOD and the precursor of the ketonic-cycle oct-1-en-3-one seems very likely. This suggests a biosynthetic route from linoleic acid to 13-HPOD, followed by a subsequent cleavage step to oct-1-en-3-one and therefore to C8-oxylipins of the ketonic-cycle.de_DE
dc.language.isoende_DE
dc.relation.hasparthttps://doi.org/10.1371/journal.pone.0218625de_DE
dc.relation.hasparthttps://doi.org/10.1007/s11557-021-01719-3de_DE
dc.relation.hasparthttps://doi.org/10.1002/cctc.202002011de_DE
dc.relation.hasparthttps://doi.org/10.1186/s13568-021-01195-8de_DE
dc.rightsIn Copyright*
dc.rights.urihttp://rightsstatements.org/page/InC/1.0/*
dc.subjectenzymesde_DE
dc.subjectbiosynthesisde_DE
dc.subjectoxylipinsde_DE
dc.subject1-octen-3-olde_DE
dc.subjectfungide_DE
dc.subject.ddcddc:500de_DE
dc.subject.ddcddc:540de_DE
dc.subject.ddcddc:570de_DE
dc.titleEnzymology of the C8-Oxylipin Biosynthesis in Cyclocybe aegeritade_DE
dc.typedoctoralThesisde_DE
dcterms.dateAccepted2022-09-13
local.affiliationFB 08 - Biologie und Chemiede_DE
thesis.levelthesis.doctoralde_DE


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