Difference between revisions of "Part:BBa K1595024:Experience"
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<p>From the results above, it is clear that the fusion protein MBP+EcnB functions notably well in combating <i>F. psychrophilum</i>. Below are the Zone of inhibition measurements for two negative controls, empty BL21 and BBa_K1460001, the positive control, oxytetracycline, and the EcnB constructs, BBa_K1595006, BBa_K1595008, BBa_K1595016, BBa_K1595024. </p> | <p>From the results above, it is clear that the fusion protein MBP+EcnB functions notably well in combating <i>F. psychrophilum</i>. Below are the Zone of inhibition measurements for two negative controls, empty BL21 and BBa_K1460001, the positive control, oxytetracycline, and the EcnB constructs, BBa_K1595006, BBa_K1595008, BBa_K1595016, BBa_K1595024. </p> | ||
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Revision as of 01:58, 21 September 2015
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how you used this part and how it worked out.
Applications of BBa_K1595024
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UNIQ043ff6c7dd1c8440-partinfo-00000000-QINU UNIQ043ff6c7dd1c8440-partinfo-00000001-QINU
Overview of Characterization of MBP+EcnB BioBrick
The peptide EcnB is capable of inhibiting the growth of F. psychrophillum in order to treat bacterial coldwater disease prevalent in salmonid species. In order to stabilize the EcnB peptide, we have placed EcnB downstream of MBP, a maltose binding protein. We have experimentally validated BBa_K1595024 to work as expected in decreasing the growth of F. psychrophillum as detailed below using lysate assays as wel as disk diffusion assays.
All lysate assay tests were run with 20 mL cytophaga media samples. The samples were inoculated from a -80℃ frozen glycerol stock of F. psychrophillum and then incubated at 15℃ for 48-72 hours. An overnight culture of EcnB-BL21 constructs were used to inoculate a preinduction culture consisting of LB and chloramphenicol (25μg/mL). The cultures were incubated at 37℃ for 6 hours and induced with L-arabinose (1% w/w). After 6 more hours of incubation at 37℃, 125 mL of culture were centrifuged at 5000g for 10 minutes. The pellets were resuspended in 1 mL phosphate buffer saline solution and homogenized (4) for 10 minutes. The lysates were centrifuged at 10000g for 10 minutes. Samples were placed either on ice or at 4℃ throughout the lysis process. The supernatants were added to the F. psychrophillum cultures. Optical density readings were performed using a spectrophotometer set at OD600. Readings were performed over 12 hours. The chart below depicts the progression of OD600 over 12 hours after the inoculation of lysate from BBa_K1595024 as compared to lysate from BL21 control and lysate from buffer control. As shown, F. psychrophillum exposed to lysate from BBa_K1595024 experienced a drop in growth as expected, whereas F. psychrophillum exposed to BL21 and buffer lysate exhibited an increase in growth.
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We further validated the efficacy of BBa_K1595024 using a series of disk diffusion assays containing lysate from BBa_K1595024, and compared the zone of inhibition to oxytetracycline (the fish farm industry standard antibiotic currently used to treat BCWD) as well as BL21 lysate as a negative control. The BBa_K1595024 zone of inhibition had an average diameter of 50.7mm, as compared to 55.2mm from oxytetracycline’s zone of inhibition (pictured below).
From the results above, it is clear that the fusion protein MBP+EcnB functions notably well in combating F. psychrophilum. Below are the Zone of inhibition measurements for two negative controls, empty BL21 and BBa_K1460001, the positive control, oxytetracycline, and the EcnB constructs, BBa_K1595006, BBa_K1595008, BBa_K1595016, BBa_K1595024.
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