The cytochrome P-450 monooxygenase and ï¢-oxidation systems of alkane-utilizing yeasts have been studied extensively, whereas very little is known about the fatty (long chain) alcohol and fatty aldehyde oxidizing enzymes. With the recent completion of sequencing of the genome of Yarrowia lipolytica, an alkane-degrading yeast, several putative aldehyde dehydrogenases (ALDHs) have been identified. Four of these were identified as fatty ALDHs (FALDHs). Northern blot analysis and RT-PCR showed that one of the FALDH genes, labelled FALDH4, is induced during growth of Y. lipolytica on alkanes, whereas another aldehyde dehydrogenase gene, labelled ALDH1, was constitutively expressed. Functional analysis of the four FALDH isogenes was initiated by single gene deletion of the four fatty aldehyde dehydrogenase isogenes in all possible combinations. The Cre-loxP recyclable tools system was used for gene disruption.
Growth properties of the triple and quadruple deletion strains on alkanes were investigated. A slightly arrested growth in hexadecane was observed in two strains, the triple deletion mutant with intact FALDH2 isogene and the quadruple deletion mutant with all four FALDH isogenes deleted. Very strong hydrophobicity during growth of these mutants in hexadecane was also observed. At this stage one can only say that disruption of FALDH isogenes had a slight negative effect on growth of this yeast on alkanes.; However, it is not yet clear which individual isogenes are the most important for alkane metabolism in this organism.
Although fatty aldehyde dehydrogenase (FALDH) activity has been detected in fungi no FALDH genes have yet been cloned, sequenced and expressed. Through BLAST searches using the human FALDH sequence as query we have identified 28 FALDH/FALDH-like gene sequences of which nine are from molds and 19 from yeast species. A comparative study of these sequences showed that fungal FALDH sequences may fall into several different subclasses of the ALDH3 family. Unique features of these proteins included presence of several transmembrane domains and in particular relatively long C- and N-termini.
Searches of the sequenced Y. lipolytica genome for fatty alcohol oxidase (FAOD) and fatty alcohol dehydrogenase (FADH) encoding genes, which could be involved in the oxidation of fatty alcohols to aldehydes, yielded only one putative FADH encoding gene. However, FADH activity during growth on n-alkanes was very low and Northern-blot analyses showed that this gene was only weakly expressed during growth on hydrocarbon and non-hydrocarbon substrates.
| Identifer | oai:union.ndltd.org:netd.ac.za/oai:union.ndltd.org:ufs/oai:etd.uovs.ac.za:etd-03282006-083232 |
| Date | 28 March 2006 |
| Creators | Matatiele, Puleng Rose |
| Contributors | Prof MS Smit, Dr J Albertyn |
| Publisher | University of the Free State |
| Source Sets | South African National ETD Portal |
| Language | en-uk |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.uovs.ac.za//theses/available/etd-03282006-083232/restricted/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University Free State or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report. |
Page generated in 0.0024 seconds