Difference between revisions of "Part:BBa K802000"
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<p>Biofilms are formed by the <i>S. aureus</i> fluorescent strain RN4220 pALC2084 expressing GFP. It is a nonmotile laboratory strain, used to form biofilm in 96-well microscopic-grade microtiter plate.<br><br/> | <p>Biofilms are formed by the <i>S. aureus</i> fluorescent strain RN4220 pALC2084 expressing GFP. It is a nonmotile laboratory strain, used to form biofilm in 96-well microscopic-grade microtiter plate.<br><br/> | ||
| − | <i>Bacillus subtilis</i> 168 transformed by pBK28 (lysostaphin in the shuttle vector) and by pBKL25 (the shuttle vector without gene to have a negative control) were grown on LB medium supplemented with erythromycin (15µg/mL).<br> | + | <i>Bacillus subtilis</i> 168 transformed by pBK28 (lysostaphin in the shuttle vector) and by pBKL25 (the shuttle vector without any gene to have a negative control) were grown on LB medium supplemented with erythromycin (15µg/mL).<br> |
| − | After 24h of culture at 30°C without shaking, | + | After 24h of culture at 30°C without shaking, biofilms were observed under a time-lapse confocal microscope.<br> |
Cells expressing GFP were excited at 488 nm with an argon laser, and fluorescent emission was collected on a detector in the range of 500-600 nm using an oil-immersion objective with a magnification of 63x. The overall three-dimensional structures of the biofilms were scanned from the solid surface to the interface with the growth medium, using a step of 1 µm.<br> | Cells expressing GFP were excited at 488 nm with an argon laser, and fluorescent emission was collected on a detector in the range of 500-600 nm using an oil-immersion objective with a magnification of 63x. The overall three-dimensional structures of the biofilms were scanned from the solid surface to the interface with the growth medium, using a step of 1 µm.<br> | ||
| − | The 3D constructions | + | The 3D constructions were obtained with IMARIS software.</p> |
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===Usage and Biology=== | ===Usage and Biology=== | ||
| − | This part was designed to be used in a motile strain like <i>Bacillus subtilis</i> 168 or <i>Bacillus thuringiensis</i> in order to cause the lysis of the <i>Staphilococcus aureus</i> cells. The motility of the strain | + | This part was designed to be used in a motile strain like <i>Bacillus subtilis</i> 168 or <i>Bacillus thuringiensis</i> in order to cause the lysis of the <i>Staphilococcus aureus</i> cells. The motility of the strain makes its penetration inside the biofilm easier. |
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Revision as of 11:30, 24 September 2012
Lysostaphin generator for B. subtilis
This part associates the Bacillus subtilis Constitutive Promoter (PVeg) with the lysostaphin gene. Lysostaphin is a bacterial biocide isolated from Staphylococcus simulans and which specifically cleaves the pentaglycine cross bridges found in the staphylococcal peptidoglycan. It contains the necessary RBS to work. With this part, Bacillus subtilis strains cause the lysis of Staphylococcus aureus cells.
Characterization
Following results show that this part allows B. subtilis 168 strains to kill the S. aureus and epidermidis cells.
In our plasmid collection, this part is named pBK23 in the backbone Chloramphenicol and pBKL28 in the shuttle vector E. coli – B. subtilis. The corresponding negative control is the shuttle vector (pBKL25 in our collection). We worked with the plasmid pBKL28 for the tests and we tried two different genetic backgrounds: the strain NM522 to make test in E. coli and the strain 168 to make test in Bacillus subtilis.
In you have any question on the following experiments, don’t forget that all the information relative to our strains, plasmids and protocols are on our wiki notebook.
Confocal Microscopy 
Biofilms are formed by the S. aureus fluorescent strain RN4220 pALC2084 expressing GFP. It is a nonmotile laboratory strain, used to form biofilm in 96-well microscopic-grade microtiter plate.
Bacillus subtilis 168 transformed by pBK28 (lysostaphin in the shuttle vector) and by pBKL25 (the shuttle vector without any gene to have a negative control) were grown on LB medium supplemented with erythromycin (15µg/mL).
After 24h of culture at 30°C without shaking, biofilms were observed under a time-lapse confocal microscope.
Cells expressing GFP were excited at 488 nm with an argon laser, and fluorescent emission was collected on a detector in the range of 500-600 nm using an oil-immersion objective with a magnification of 63x. The overall three-dimensional structures of the biofilms were scanned from the solid surface to the interface with the growth medium, using a step of 1 µm.
The 3D constructions were obtained with IMARIS software.
S.aureus biofilm no treated (Blank)
S.aureus biofilm treats by the strain with the part
SDS-PAGE Protein gel
OD(600nm) Test
Usage and Biology
This part was designed to be used in a motile strain like Bacillus subtilis 168 or Bacillus thuringiensis in order to cause the lysis of the Staphilococcus aureus cells. The motility of the strain makes its penetration inside the biofilm easier.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 1316
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]