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[Objective] To distinguish Gentiana straminea Maxim. from wild and cultivated plants by comparing chloroplast DNA psbA-trnH sequences, so as to provide a molecular basis for origin identification and quality evaluation.[Method] The cpDNA psbA-trnH sequences of Gentiana straminea Maxim. were amplified by polymerase chain reaction (PCR), and then sequenced by direct PCR sequencing method for homologous analysis. [Result] The lengths of cpDNA psbA-trnH from wild and cultivated plants were 316 and 317 bp respectively, and there were 4 variable sites.[Conclusion] The nucleotide differences of psbA-trnH regions could be used for distinguishing Gentiana straminea Maxim. from wild and cultivated plants.
[Objective] To distinguish Gentiana straminea Maxim. From wild and cultivated plants by comparing chloroplast DNA psbA-trnH sequences, so as to provide molecular basis for origin identification and quality evaluation. [Method] The cpDNA psbA-trnH sequences of Gentiana straminea Maxim . were amplified by polymerase chain reaction (PCR), and then sequenced by direct PCR sequencing method for homologous analysis. [Result] The lengths of cpDNA psbA-trnH from wild and cultivated plants were 316 and 317 bp respectively, and there were 4 variable sites. [Conclusion] The nucleotide differences of psbA-trnH regions could be used for distinguishing Gentiana straminea Maxim. from wild and cultivated plants.