ISSN: 0973-7510

E-ISSN: 2581-690X

Zhengquan Gao1, Chunxiao Meng1 , Hongzheng Gao1, Naihao Ye2, Xiaowen Zhang2, Yuanfeng Su1, Yuren Zhao1 and Yuanyuan Wang1
1School of Life Sciences, Shandong University of Technology, Zibo 255049, China.
2Yellow Sea Fishery Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China.
J Pure Appl Microbiol. 2013;7(4):2503-2511
© The Author(s). 2013
Received: 12/04/2013 | Accepted: 25/06/2013 | Published: 30/12/2013
Abstract

The freshwater eukaryotic unicellular alga Haematococcus pluvialis is one of the best sources to produce natural astaxanthin in nature. However, the regulatory role of carotenogenesis leading to astaxanthin formation is not well understood. In this study, the effects of ET on transcriptional expressions of eight carotenoid genes in H. pluvialis were measured using qRT-PCR. Results showed that eight carotenogenic genes were up-regulated by ET with different expression profiles. Astaxanthin accumulation was promoted efficiently by ET, which might result from the up-regulating of ipi-1, ipi-2, pds, lyc, bkt, crtR-b and crtO at the transcriptional level, and by psy at both transcriptional and post-transcriptional levels. Moreover, fourteen proteins were expressed differentially in ET treatments compared to controls. Furthermore, algal cell division accompanying accompanied by astaxanthin accumulation for the first time during the whole course of ethylene induction. The knowledge in the present paper might help to optimize the physiological conditions needed to produce a high yield of astaxanthin with ET.

Keywords

Haematococcus pluvialis, Astaxanthin, Ethylene (ET), Regulation, Carotenoid genes, Real-time fluorescence quantitative PCR (qRT-PCR)

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