2008Anhui nongye kexueRequires access

Study on the Cloning and Sequence Analysis of FADX Gene from Vernicia fordii

Li Yuan

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Abstract

[Objective] The research aimed to clone full-length cDNA of FADX of Vernicia fordii seeds.The bioinformatic analysis of this gene was done,and provided reference for the further research of the function of gene.[Method] Total RNA were successfully extracted by developing Vernicia fordii seeds with improved TRIzoL method.Primer was designed according to the FADX sequences recorded in Genbank.Full-length cDNA of FADX was obtained by cloning it with RT-PCR method.Bioinformatic analysis were done by using the software of Antheprot and Interproscan.[Result] The length of 5' side and 3' side unencoded area's sequences were 13 bp and 47 bp,contained an opening reading frame from 14 bp to 1 174 bp which encoded a polypeptide of 386 amino acids,and contained a specific fattic acid dehydrogenase structural domain.Relative molecular weight was 44 343.0,pI was 8.33,and the calculation of secondary structure showed that the protein contained 29% in α-helix,32% in β-pleated sheet,and 6% inβ-return.[Conclusion] This protein had the property of fattic acid dehydrogenase.

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What this paper is about

[Objective] The research aimed to clone full-length cDNA of FADX of Vernicia fordii seeds.The bioinformatic analysis of this gene was done,and provided reference for the further research of the function of gene.[Method] Total RNA were successfully extracted by developing Vernicia fordii seeds with improved TRIzoL method.Primer was designed according to the FADX sequences recorded in Genbank.Full-length cDNA of FADX was obtained by cloning it with RT-PCR method.Bioinformatic analysis were done by using the software of Antheprot and Interproscan.[Result] The length of 5' side and 3' side unencoded area's sequences were 13 bp and 47 bp,contained an opening reading frame from 14 bp to 1 174 bp which encoded a polypeptide of 386 amino acids,and contained a specific fattic acid dehydrogenase structural domain.Relative molecular weight was 44 343.0,pI was 8.33,and the calculation of secondary structure showed that the protein contained 29% in α-helix,32% in β-pleated sheet,and 6% inβ-return.[Conclusion] This protein had the property of fattic acid dehydrogenase.

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Available abstract

[Objective] The research aimed to clone full-length cDNA of FADX of Vernicia fordii seeds.The bioinformatic analysis of this gene was done,and provided reference for the further research of the function of gene.[Method] Total RNA were successfully extracted by developing Vernicia fordii seeds with improved TRIzoL method.Primer was designed according to the FADX sequences recorded in Genbank.Full-length cDNA of FADX was obtained by cloning it with RT-PCR method.Bioinformatic analysis were done by using the software of Antheprot and Interproscan.[Result] The length of 5' side and 3' side unencoded area's sequences were 13 bp and 47 bp,contained an opening reading frame from 14 bp to 1 174 bp which encoded a polypeptide of 386 amino acids,and contained a specific fattic acid dehydrogenase structural domain.Relative molecular weight was 44 343.0,pI was 8.33,and the calculation of secondary structure showed that the protein contained 29% in α-helix,32% in β-pleated sheet,and 6% inβ-return.[Conclusion] This protein had the property of fattic acid dehydrogenase.

Key concepts: Trizol, GenBank, Cloning (programming), Open reading frame, Protein secondary structure, Complementary DNA, clone (Java method), Gene

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