Abstract
A pBBad22T-derived conditioned arabinose (Ara)-inducible expression system was evaluated in Stenotrophomonas maltophilia (an opportunistic pathogen and has gained increasing attention as a cause of healthcare-associated infection). S. maltophilia cannot grow well when Ara is the sole available carbon source. The induction kinetic study, optimal inducer concentration determination, and depletion experiment were performed by using a xylE gene fusion construct, pBxylE, to monitor the expression of pBBad22T in S. maltophilia. For induction survey, the expression of catechol 2,3-dioxygenase (C23O), encoded by xylE gene, continuously increases during an 8-h induced course and can be modulated by different inducer concentrations. The applied induction condition of pBBad22T in S. maltophilia is the inducer concentration ranging from 0.1% to 0.5% for an induction time of 4 h. For repression evaluation, the C23O expression is rapidly turned off within 30 min after the removal of Ara. Accordingly, the established Ara-inducible system can provide a convenient tool for the study of S. maltophilia.
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Abbreviations
- Ap:
-
Ampicilin
- Ara:
-
Arabinose
- BHR:
-
Broad host range
- C23O:
-
Catechol 2,3-dioxygenase (EC 1.13.11.2)
- Km:
-
Kanamycin
- LB:
-
Luria–Bertani
- MCS:
-
Multiple cloning site(s)
- R:
-
Resistance/resistant
- Tet:
-
Tetracycline
- xylE :
-
Gene encoding C230
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Acknowledgments
This research was supported by grant CMU-99-S-42 from the China Medical University and grant NSC 98-2320-B-039-011-MY3 from the National Science Council.
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Huang, YW., Hu, RM., Chiang, YT. et al. Establishment of an arabinose-inducible system in Stenotrophomonas maltophilia . Folia Microbiol 56, 18–22 (2011). https://doi.org/10.1007/s12223-011-0008-2
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DOI: https://doi.org/10.1007/s12223-011-0008-2