Over-expression of proteins using a modified pBAD24 vector in E. coli expression system

A modified pBAD24 vector (pBAD24M) was constructed with the araBAD promoter of the arabinose operon along with T7g10 sequence elements and a modified Shine-Dalgarno sequence. While both green fluorescent protein and granulocyte colony stimulating factor showed negligible expression under the origina...

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Veröffentlicht in:Biotechnology letters 2009-07, Vol.31 (7), p.1031-1036
Hauptverfasser: Banerjee, Sampali, Salunkhe, Shardul S, Apte-Deshpande, Anjali D, Mandi, Naganath S, Mandal, Goutam, Padmanabhan, Sriram
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Sprache:eng
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Zusammenfassung:A modified pBAD24 vector (pBAD24M) was constructed with the araBAD promoter of the arabinose operon along with T7g10 sequence elements and a modified Shine-Dalgarno sequence. While both green fluorescent protein and granulocyte colony stimulating factor showed negligible expression under the original pBAD24 vector, they were expressed at >35% of total cellular protein with the modified vector. Similar results were obtained for staphylokinase wherein the pBAD24-SAK construct yielded 8 ng/10⁶ c.f.u. of E. coli induced cells while the pBAD24M-SAK vector showed nearly 55 ng/10⁶ c.f.u. induced bacterial cells as tested by ELISA. Interestingly, the expression levels using modified pBAD24 vector matched that achieved with T7 promoter based vector system. The modified pBAD24 vector therefore represents a simple and a useful prokaryotic expression system for efficient repression, modulation and elevated protein expression levels.
ISSN:0141-5492
1573-6776
DOI:10.1007/s10529-009-9976-6