Cloning, expression and functional validation of drought inducible ascorbate peroxidase (Ec-apx1) from Eleusine coracana

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• 作者：Deepesh Bhatt (1)
  Saurabh C. Saxena (2)
  Sourabh Jain (3)
  Anoop K. Dobriyal (4)
  Manoj Majee (2)
  Sandeep Arora (1)
  
• 关键词：Cloning ; Expression ; Ascorbate peroxidase ; Drought stress
• 刊名：Molecular Biology Reports
• 出版年：2013
• 出版时间：February 2013
• 年：2013
• 卷：40
• 期：2
• 页码：1155-1165
• 全文大小：822KB
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• 作者单位：Deepesh Bhatt (1)
  Saurabh C. Saxena (2)
  Sourabh Jain (3)
  Anoop K. Dobriyal (4)
  Manoj Majee (2)
  Sandeep Arora (1)
  
  1. Department of Molecular Biology and Genetic Engineering, College of Basic Sciences and Humanities, GB Pant University of Agriculture and Technology, Pantnagar, Uttarakhand, India
  2. National Institute of Plant Genome Research, Aruna Asaf Ali Marg, New Delhi, India
  3. National Research Centre on Plant Biotechnology, Pusa Campus, New Delhi, India
  4. Department of Biotechnology, HNB Garwal University (Uttarakhand), Pauri Campus, Srinagar, India
  
• ISSN：1573-4978

文摘

Eleusine coracana (finger millet) is a stress-hardy but under-utilized cereal crop that possesses an efficient antioxidant defense system. The plant is capable of enduring long durations of water deficit stress. Experiments were conducted to clone a potent stress responsive isoform of ascorbate peroxidase and validate its role under drought stress. Reverse transcriptase PCR was used to obtain the partial cDNA of apx1 gene, from a meticulously screened drought tolerant genotype of E. coracana (PR202). Using RACE strategy, the full length apx1 cDNA was cloned and sequenced. The cDNA length of the E. coracana apx1 (Ec-apx1) gene is 1,047?bp with a 750?bp ORF, encoding a 250 amino acid protein having a molecular weight of 28.5?kDa. The identity of the amino acid sequence, deduced from the cDNA, with the APX family homologs was about 74-7?%. The full-length apx1 ORF was sub-cloned in a prokaryotic expression vector pET23b. The recombinant fusion protein, Ec-apx1, had high expression level in BL21 strain of E. coli and exhibited APX enzyme activity. The structure–function relationship of the protein was deduced by modelling a three-dimensional structure of Ec-apx1, on the basis of comparative homology using SWISS-MODEL. Real time PCR analysis of Ec-apx1 expression at mRNA level showed that the transcript increased under drought stress, with maximum levels attained 5-days after imposition of stress. Our results suggest that Ec-apx1 has a distinct pattern of expression and plays a pivotal role in drought stress tolerance. Therefore, the cloned isoform of ascorbate peroxidase can be used for developing stress tolerant genotypes of important crops, through transgenic approach.