4.1 Article

Cyclobutane pyrimidine dimers photolyase from extremophilic microalga: Remarkable UVB resistance and efficient DNA damage repair

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.mrfmmm.2014.07.010

关键词

Chlamydomonas sp ICE-L; UV; Photolyase; Photo-reactivation

资金

  1. 18th China Antarctic Project
  2. National Natural Science Foundation of China [31200097, U1406402, 31200272]
  3. Young Marine Science Foundation, SOA [2013106]
  4. Fundamental Research Funds of the First Institute of Oceanography, SOA [2013G32]
  5. Open Research Fund of Key Lab of Marine Bioactive Substance and Modern Analytical Technique, SOA [MBSMAT-2012-08]
  6. Foundation of the Key Laboratory for Ecological Environment in Coastal Areas of the State Oceanic Administration [201112]
  7. Open Research Fund of State Key Laboratory of Biological Fermentation Engineering of Beer [K2012007, K2012003]

向作者/读者索取更多资源

Bacteria living in the Antarctic region have developed several adaptive features for growth and survival under extreme conditions. Chlamydomonas sp. ICE-Lis well adapted to high levels of solar UV radiation. A putative photolyase was identified in the Chlamydomonas sp. ICE-L transcriptome. The complete cDNA sequence was obtained by RACE-PCR. This PHR encoding includes a polypeptide of 579 amino acids with clear photolyase signatures belonging to class II CPD-photolyases, sharing a high degree of homology with Chlamydomonas reinhardtii (68%). Real-time PCR was performed to investigate the potential DNA damage and responses following UVB exposure. CPD photolyase mRNA expression level increased over 50-fold in response to UVB radiation for 6 h. Using photolyase complementation assay, we demonstrated that DNA photolyase increased photo-repair more than 116-fold in Escherichia coil strain SY2 under 100 mu w/cm(2) UVB radiation. To determine whether photolyase is active in vitro, CPD photolyase was over-expressed. It was shown that pyrimidine dimers were split by the action of PHR2. This study reports the unique structure and high activity of the enzyme. These findings are relevant for further understanding of molecular mechanisms of photo-reactivation, and will accelerate the utilization of photolyase in the medical field. (C) 2015 Elsevier B.V. All rights reserved.

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