Cloning of ACC Oxidase Gene and Construction of Antisense Vector on Peony
LU Jun-gang
Abstract
LU Jun-gang
Abstract
As a respiration climacteric flower,the peony fresh (cut) flower release some endogenous ethylene which can impact aging strongly with the flower senescence.The ACC(1-aminocyclopropane-1-carboxylic acid) oxidase was one of the key rate-limiting enzymes for ethylene biosynthesis in higher plants.The studies on the expression and regulation-control of ACC oxidase have some important roles in prolonging the florescence.A pair of specific primers,P1 and P2,were designed and synthesized according to the reported cDNA sequence of the ACC oxidase gene of peony(the sequ-ence number in the GenBank was DQ337251) in this experiment.A DNA frag-ment was obtained from luoyanghonggenomic DNA by PCR at first,and linked it to pMD18-T which was a cloning vector.Then sequencing the cloned fragment.The result shows that the whole length of the fragment was 467bp.A sequence,157bp among them,might be an intron.The homologous rate of the remaining sequence was 98.2% compared with the reported sequence.The recombined plasmid and the plant expression vector pBI 121 were digested with the Sac I and Xba I.The fragment of ACC oxidase gene from peony and pBI 121 were reclaimed and ligated,an antisense expression vector was constructed in the end.
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As a respiration climacteric flower,the peony fresh (cut) flower release some endogenous ethylene which can impact aging strongly with the flower senescence.The ACC(1-aminocyclopropane-1-carboxylic acid) oxidase was one of the key rate-limiting enzymes for ethylene biosynthesis in higher plants.The studies on the expression and regulation-control of ACC oxidase have some important roles in prolonging the florescence.A pair of specific primers,P1 and P2,were designed and synthesized according to the reported cDNA sequence of the ACC oxidase gene of peony(the sequ-ence number in the GenBank was DQ337251) in this experiment.A DNA frag-ment was obtained from luoyanghonggenomic DNA by PCR at first,and linked it to pMD18-T which was a cloning vector.Then sequencing the cloned fragment.The result shows that the whole length of the fragment was 467bp.A sequence,157bp among them,might be an intron.The homologous rate of the remaining sequence was 98.2% compared with the reported sequence.The recombined plasmid and the plant expression vector pBI 121 were digested with the Sac I and Xba I.The fragment of ACC oxidase gene from peony and pBI 121 were reclaimed and ligated,an antisense expression vector was constructed in the end.
Key concepts: Complementary DNA, Cloning (programming), GenBank, Gene, Biology, Expression vector, Oxidase test, Molecular biology