Polymerase chain reaction and cloning of Burkholderia pseudomallei putative genes.
Total of 23 putative Open Read Farms from B. pseudomallei strain D286 was successfully cloned and the nucleotide sequence analysis of the putative genes showed the homologue (98-100%) to strain K96243. The high similarity in gene sequences between these strains is confirmed for presence of the neces...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English English |
| Published: |
Medwell Publishing
2009
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| Online Access: | http://psasir.upm.edu.my/id/eprint/16240/1/Polymerase%20chain%20reaction%20and%20cloning%20of%20Burkholderia%20pseudomallei%20putative%20genes.pdf http://psasir.upm.edu.my/id/eprint/16240/ |
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| Summary: | Total of 23 putative Open Read Farms from B. pseudomallei strain D286 was successfully cloned and the nucleotide sequence analysis of the putative genes showed the homologue (98-100%) to strain K96243. The high similarity in gene sequences between these strains is confirmed for presence of the necessary ORF for LPS biosynthesis through PCR amplification the application of the ORFs in the PCR amplification and expression method. The findings of this study have contributed to some information on the molecular bases of the LPS biosynthesis genes in B. pseudomallei specifically for strain D286. PCR amplification, a specific pair of primer for each ORFs was proving specific for amplification of genes in B. pseudomallei strain D286. The PCR mixture with addition of DMSO, formamide and glycerol could ease the PCR optimization where different pairs of primers were involved. The specific primer pairs with the PCR mixture could be used in developing a PCR diagnosis of melioidosis. |
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