Difference between revisions of "Part:BBa K2922043"
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1. C. Hui et al., Surface display of PbrR on Escherichia coli and evaluation of the bioavailability of lead associated with engineered cells in mice. Sci Rep 8, 5685 (2018). | 1. C. Hui et al., Surface display of PbrR on Escherichia coli and evaluation of the bioavailability of lead associated with engineered cells in mice. Sci Rep 8, 5685 (2018). | ||
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2. C. Y. Hui, Y. Guo, X. Q. Yang, W. Zhang, X. Q. Huang, Surface display of metal binding domain derived from PbrR on Escherichia coli specifically increases lead(II) adsorption. Biotechnol Lett 40, 837-845 (2018). | 2. C. Y. Hui, Y. Guo, X. Q. Yang, W. Zhang, X. Q. Huang, Surface display of metal binding domain derived from PbrR on Escherichia coli specifically increases lead(II) adsorption. Biotechnol Lett 40, 837-845 (2018). | ||
Revision as of 15:06, 19 October 2019
Expression system of DsbA-PbBD coding periplasm display of lead binding peptide with T7 promoter
Summary
This part is constructed for high expression of DsbA-PbBD(periplasm display of lead binding peptide). We replaced MBP in BBa_K346030 with PbBD to enhance the lead absorption efficiency.
Characterization
Inductively coupled plasma mass spectrometry (ICP-MS) was used to accurately test the absorption amount of lead per unit mass of cells. BL21 (DE3) with DsbA-MBP and DsbA-PbBD integration plasmids were separately cultured in medium containing 50 μM Pb(II). The amounts of lead absorbed by the bacteria with different circuits were measured. And as the experimental results shown in Fig.2, the lead absorption efficiency of DsbA-PbBD group was better than that in DsbA-MBP group.
Reference
1. C. Hui et al., Surface display of PbrR on Escherichia coli and evaluation of the bioavailability of lead associated with engineered cells in mice. Sci Rep 8, 5685 (2018).
2. C. Y. Hui, Y. Guo, X. Q. Yang, W. Zhang, X. Q. Huang, Surface display of metal binding domain derived from PbrR on Escherichia coli specifically increases lead(II) adsorption. Biotechnol Lett 40, 837-845 (2018).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 317
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 149
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 715