Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/30373
Title: Characterization of carotenoid hydroxylase gene promoter in Haematococcus pluvialis
Authors: Meng, C X
Wei, W
Su, Z-L
Qin, S
Keywords: Haematococcus pluvialis;Astaxanthin;Carotenoid hydroxylase;cis-Acting element;Promoter
Issue Date: Oct-2006
Publisher: NISCAIR-CSIR, India
Abstract: Astaxanthin, a high-value ketocarotenoid is mainly used in fish aquaculture. It also has potential in human health due to its higher antioxidant capacity than β-carotene and vitamin E, The unicellular green alga Haematococcus pluvialis is known to accumulate astaxanthin in response to environmental stresses, such as high light intensity and salt stress. Carotenoid hydroxylase plays a key role in astaxanthin biosynthesis in H. pluvialis. In this paper, we report the characterization of a promoter-like region (-378 to -22 bp) of carotenoid hydroxylase gene by cloning, sequence analysis and functional verification of its 919 bp 5'-flanking region in H. pluvialis. The 5’-flanking region was characterized using micro-particle bombardment method and transient expression of LacZ reporter gene. Results of sequence analysis showed that the 5’-flanking region might have putative cis-acting elements, such as ABA (abscisic acid)-responsive element (ABRE), Crepeat/ dehydration responsive element (C-repeat/DRE), ethylene-responsive element (ERE), heat-shock element (HSE), wound-responsive element (WUN-motif), gibberellin-responsive element (P-box), MYB-binding site (MBS) etc., except for typical TATA and CCAAT boxes. Results of 5' deletions construct and β-galactosidase assays revealed that a highest promoter-like region might exist from -378 to -22 bp and some negative regulatory elements might lie in the region from -919 to -378 bp. Results of site-directed mutagenesis of a putative C-repeat/DRE and an ABRE-like motif in the promoterlike region (-378 to -22 bp) indicated that the putative C-repeat/DRE and ABRE-like motif might be important for expression of carotenoid hydroxylase gene.
Page(s): 284-288
URI: http://hdl.handle.net/123456789/30373
ISSN: 0975-0959 (Online); 0301-1208 (Print)
Appears in Collections:IJBB Vol.43(5) [October 2006]

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