Utane RungpanichSupinya PongsunkTakayuki EzakiPattama EkpoMahidol UniversitySrinakharinwirot UniversityGifu University2018-09-132018-09-132009-03-01Southeast Asian Journal of Tropical Medicine and Public Health. Vol.40, No.2 (2009), 295-301012515622-s2.0-63149121299https://repository.li.mahidol.ac.th/handle/20.500.14594/28178The 30 kDa protein of B. pseudomallei is found in virulent Ara- but not avirulent Ara+ strain. The gene was cloned in Escherichia coli JM105 employing pInIII-C2 vector. The open reading frame was 870 nucleotides with a guanine plus cytosine content of 69.9%. Arginine was the most abundant amino acid in the protein, having a PI of 12.65. Nucleotide sequence of the gene was 96% identical to B. pseudomallei 1710b chromosome II sequence CP000125.1, encoding an oxidoreductase of the short chain dehydrogenase/ reductase family. The 30 kDa antigen was expressed as a maltose-fusion protein with a yield of 5.25 mg/l of bacterial culture.Mahidol UniversityMedicineExpression and purification of 30 kilodalton protein antigen of ARA <sup>-</sup>Burkholderia pseudomalleiArticleSCOPUS