• Medientyp: E-Book; Hochschulschrift
  • Titel: Microbial production of Poly(3-hydroxybutyrate-3- hydroxyvalerate)-copolymers from starch-containing byproducts
  • Beteiligte: Biernacki, Mateusz [VerfasserIn]; Schüller, Hans-Joachim [AkademischeR BetreuerIn]; Passoth, Volkmar [AkademischeR BetreuerIn]
  • Körperschaft: Universität Greifswald
  • Erschienen: Greifswald, 2018
  • Umfang: 1 Online-Ressource (PDF-Datei: 130 Seiten, 2388 Kilobyte); Illustrationen (teilweise farbig), Diagramme (teilweise farbig)
  • Sprache: Englisch; Deutsch
  • Identifikator:
  • Schlagwörter: Mikrobiologie > Arxula adeninivorans > Polyhydroxyfettsäuren > Stärke > Biokunststoff > Kunststoffherstellung
  • Entstehung:
  • Hochschulschrift: Dissertation, Mathematisch-Naturwissenschaftliche Fakultät der Universität Greifswald, 2019
  • Anmerkungen: Literaturverzeichnis: Seite 106-114
    Zusammenfassungen in deutsch und englisch
  • Beschreibung: Mikrobiologie, Stärke, Starch, Yeast, poly(hydroxyalkanoates)

    Currently, plastic materials are an integral part of our lives, but their production mostly bases on fossil fuels or derivatives, which resources are decreasing. Extraction and processing of non-renewable resources have also negative impact on environment. One of the most promising and environmentally friendly approaches is use of microorganism. This PhD dissertation presents the non-conventional yeast Arxula adeninivorans as a host for production of bio-based and biodegradable poly(hydroxyalkanoates) plastics poly(hydroxybutyrate) and co-polymer poly(hydroxybutyrate-co-hydroxyvalerate). Additionally, the constructed yeast strain was able to secrete enantiomerically pure (R)-3-hydroxybutyric acid. The production of PHAs requires three enzymes: β-ketothiolase, acetoacetyl-CoA reductase and PHA synthase. The strategy followed in this project was divided into two parts. While all three enzymes are responsible for intracellular production of PHA polymer, first two only lead to secretion of (R)-3-HB into culture media, which was used in a first stage of work to establish and optimize polymer production. Both, different bacterial strains and yeast A. adeninivorans were taken into account in screening of the genes encoding aforementioned enzymes. Bacterial genes were chemically synthesized using codon optimization pattern and endogenous genes were obtained using PCR and genomic DNA template from A. adeninivorans LS3 wild-type strain. Each gene was cloned into Xplor2 vector between ...
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