Abstract
CYP450 plays an important role in physiological metabolism. A CYP4G25 gene of P450 family was cloned from Antheraea pernyi using reverse transcriptase-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA end (RACE-PCR). Sequence analysis revealed that this gene was 2112 bp long and has 97.5% identity with Antheraea yamamai CYP4G25. Semi-quantitative polymerase chain reaction (PCR) showed that the expression of A. pernyi CYP4G25 was found in various tissues with no significant changes. Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and western blot analysis demonstrated that a 63.6 KD recombinant protein was successfully expressed in Escherichia coli cells and its expression was not remarkably changed under induction by different isopropyl-β-D-thiogalactopyranoside (IPTG) concentration. © 2011 Academic Journals.
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Liu, Q., Liu, C., Zhu, B., Cao, J., Wei, G., Qian, C., … Sun, Q. (2011). Identification and expression analysis of CYP4G25 gene from the Chinese oak silkworm (Antheraea pernyi). African Journal of Biotechnology, 10(42), 8205–8212. https://doi.org/10.5897/ajb10.2658
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