| Literature DB >> 28751049 |
Faten Ben Amor1, Mohamed Barkallah2, Fatma Elleuch1, Nesrine Karkouch1, Mouna Dammak2, Bruno Baréa3, Pierre Villeneuve3, Slim Abdelkafi2, Imen Fendri4.
Abstract
The blue-green microalga, Arthrospira sp., isolated from the sea of Kssour Essef in Mahdia (Tunisia), was purified and then identified both morphologically and genetically based on 16S rRNA gene sequence. Following physicochemical analysis, the prokaryotic microalga tested represented a competitive source of pigments and showed a considerable rate in protein (64%) which was confirmed by FTIR measurement. The lipid content (4%) was quantified by the gravimetric method and the intracellular lipid bodies were detected with the Nile red staining. Using gas chromatography coupled with flame ionization detector, the fatty acid profile revealed the presence of 27.4% and 32.88% of monounsaturated fatty acids (MUFAs) and polyunsaturated fatty acids (PUFAs), respectively. Given the richness of the isolated microalga in unsaturated fatty acids, we have developed a SYBR Green real time PCR method for the specific identification of Arthrospira sp. Δ9 desaturase gene. This current method will be of great value for carrying out high-throughput studies like cloning, heterologous expression and structure-function relationship analysis.Entities:
Keywords: 16S rDNA sequencing; Arthrospira sp.; Lipids; RT-PCR; Δ9 desaturase gene
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Year: 2017 PMID: 28751049 DOI: 10.1016/j.ijbiomac.2017.07.139
Source DB: PubMed Journal: Int J Biol Macromol ISSN: 0141-8130 Impact factor: 6.953