Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692349
Title: Biotechnological exploitation of Chlamydomonas reinhardtii
Author: Gangl, Doris
ISNI:       0000 0004 5918 2806
Awarding Body: University of Kent
Current Institution: University of Kent
Date of Award: 2016
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Abstract:
Microalgae have become increasingly important in the biotech sector and are currently exploited for their natural products. In recent years efforts have also been directed towards establishing them as production platforms for recombinant proteins. The aim of this thesis is to investigate the feasibility of Chlamydomonas reinhardtii as a production platform for highvalue products expressed in the chloroplast of the alga. A cytochrome P450 was introduced into the chloroplast of C. reinhardtii as a proof-of-concept study. The model enzyme CYP79A1 was successfully targeted into the chloroplast membranes and was found to be active. A bifunctional diterpene synthase, TPS4, was also expressed in the chloroplast of C. reinhardtii. TPS4 could be purified to homogeneity and is the largest enzyme expressed in the chloroplast to date. The two transgenic strains expressing CYP79A1 and TPS4 were investigated for their ability to withstand industrial growth conditions. The cell wall deficient strains were successfully cultivated in 100 L photobioreactors using a mixotrophic growth regime. They reached dry weights of 0.3 g/L and the expression of CYP79A1 and TPS4 was detected over the entire growth period. Taken together these data suggest that C. reinhardtii could be an attractive platform for recombinant protein production. Two enzymes with biotechnological relevance were expressed in the chloroplast of the alga and the transgenic cell wall deficient strains were successfully cultivated on a semi-industrial scale.
Supervisor: Robinson, Colin Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.692349  DOI: Not available
Keywords: QH541 Ecology
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