Preeyanan AnwisedThai KabbuaTheeranan TemsiripongApisak DhiravisitSarawut JitrapakdeeTomohiro ArakiKazunari YonedaSompong ThammasirirakKhon Kaen UniversitySriracha Moda Co.Mahidol UniversityTokai University2018-10-192018-10-192013-03-01Protein Journal. Vol.32, No.3 (2013), 172-18215734943157238872-s2.0-84876413063https://repository.li.mahidol.ac.th/handle/20.500.14594/31357The first report of complete nucleotide sequences for α- and β-globin chains from the Siamese hemoglobin (Crocodylus siamensis) is given in this study. The cDNAs encoding α- and β-globins were cloned by RT-PCR using the degenerate primers and by the rapid amplification of cDNA ends method. The full-length α-globin cDNA contains an open reading frame of 423 nucleotides encoding 141 amino acid residues, whereas the β-globin cDNA contains an open reading frame of 438 nucleotides encoding 146 amino acid residues. The authenticity of both α- and β-globin cDNA clones were also confirmed by the heterologous expression in Escherichia coli (E. coli). This is the first time that the recombinant C. siamensis globins were produced in prokaryotic system. Additionally, the heme group was inserted into the recombinant proteins and purified heme-bound proteins were performed by affinity chromatography using Co2+-charged Talon resins. The heme-bound proteins appeared to have a maximum absorbance at 415 nm, indicated that the recombinant proteins bound to oxygen and formed active oxyhemoglobin (HbO2). The results indicated that recombinant C. siamensis globins were successfully expressed in prokaryotic system and possessed an activity as ligand binding protein. © 2013 Springer Science+Business Media New York.Mahidol UniversityBiochemistry, Genetics and Molecular BiologyChemical EngineeringChemistryArticleSCOPUS10.1007/s10930-013-9474-5