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Introducing and Detecting L-forms in Plants
From 2013.igem.org
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| - | + | {{Team:Newcastle}} | |
| - | + | ==Introducing and detecting L-forms in Plants== | |
| - | + | ===Detecting L-forms in Plants Using gusA Reporter Gene=== | |
| - | 2) Transformed L-forms will be selected by antibiotic resistance | + | <b>Transformation B.subtilis to contain gusA</b> |
| + | |||
| + | 1) Transform L-forms of B. subtilis NCIMB8054. | ||
| + | |||
| + | 2) Transformed L-forms will be selected by antibiotic resistance. | ||
| + | |||
| + | 3) Conduct southern hybridization to confirm the integration of the gusA gene. | ||
| - | |||
'''Production of L-form containing Plants''' | '''Production of L-form containing Plants''' | ||
| Line 19: | Line 24: | ||
4) Wash seeds with transformed L-forms. | 4) Wash seeds with transformed L-forms. | ||
| - | 5) Wash plants with | + | 5) Wash plants with deionised water to lyse extracellular L-forms. |
6) Incubate plants. | 6) Incubate plants. | ||
| Line 25: | Line 30: | ||
'''Visualisation of L-forms in plants''' | '''Visualisation of L-forms in plants''' | ||
| - | 1) Heat seeds in a vacuum oven with | + | 1) Heat seeds in a vacuum oven with GUS staining solution. |
2) Incubate at 37 degrees. | 2) Incubate at 37 degrees. | ||
| Line 35: | Line 40: | ||
1) Extract DNA from transformed L-form B. subtilis, L-form control and non L-form B.subtilis. | 1) Extract DNA from transformed L-form B. subtilis, L-form control and non L-form B.subtilis. | ||
| - | 2) PCR: Use primers specific for | + | 2) PCR: Use primers specific for gusA gene in a PCR to show gus A gene is present in transformed L-forms only. |
'''Re-isolation of L-forms from seeds''' | '''Re-isolation of L-forms from seeds''' | ||
| Line 45: | Line 50: | ||
3) Macerate seeds with pestle. | 3) Macerate seeds with pestle. | ||
| - | 4) Plate out 100ul of suspension onto | + | 4) Plate out 100ul of suspension onto L-phase medium (which is designed for the growth of L-forms) and nutrient agar and incubate (also repeat using 100ul of original bacterial suspension on each of agar). |
5) Look for signs of life, L-form or otherwise. | 5) Look for signs of life, L-form or otherwise. | ||
| - | =GusA Reporter Gene= | + | ===GusA Reporter Gene=== |
Gus A reporter gene encodes beta-glucornide (GUS) an enzyme in Escherichia coli. | Gus A reporter gene encodes beta-glucornide (GUS) an enzyme in Escherichia coli. | ||
BioBrick Part: BBa_K330002 | BioBrick Part: BBa_K330002 | ||
[http://partsregistry.org/Part:BBa_K330002:Experience] | [http://partsregistry.org/Part:BBa_K330002:Experience] | ||
| + | |||
| + | ===Detecting L-forms in Plants Using Red Flourescent Protein (RFP)=== | ||
| + | '''Transformation B.subtilis to contain RFP gene''' | ||
| + | |||
| + | 1) Transform L-forms of B. subtilis NCIMB8054. | ||
| + | |||
| + | 2) Transformed L-forms will be selected by antibiotic resistance. | ||
| + | |||
| + | 3) Conduct southern hybridization to confirm the integration of the RFP gene. | ||
| + | |||
| + | |||
| + | '''Production of L-form containing Plants''' | ||
| + | |||
| + | 1) Wash seeds. | ||
| + | |||
| + | 2) Grow seeds in petri dishes. | ||
| + | |||
| + | 3) Incubate until radicals had just emerge. | ||
| + | |||
| + | 4) Wash seeds with transformed L-forms. | ||
| + | |||
| + | 5) Wash plants with distillled water to lyse extracellular L-forms. | ||
| + | |||
| + | 6) Incubate plants. | ||
| + | |||
| + | '''Show RFP gene is only present in transformed L-forms''' | ||
| + | |||
| + | 1) Extract DNA from transformed L-form B. subtilis, L-form control and non L-form B.subtilis. | ||
| + | |||
| + | 2) PCR: Use primers specific for RFP gene in a PCR to show gus A gene is present in transformed L-forms only. | ||
| + | |||
| + | '''Re-isolation of L-forms from seeds''' | ||
| + | |||
| + | 1) Wash seeds treated with L-form bacteria or mannitol control with distilled water to remove any L-forms on the plant surface. | ||
| + | |||
| + | 2) Place seeds in in mannitol solution. | ||
| + | |||
| + | 3) Macerate seeds with pestle. | ||
| + | |||
| + | 4) Plate out 100ul of suspension onto L-phase medium and nutrient agar and incubate (also repeat using 100ul of original bacterial suspension for each agar). | ||
| + | |||
| + | 5) Look for signs of life, L-form or otherwise. | ||
| + | |||
| + | ===Alternative Methods Considered=== | ||
| + | '''Enzyme-linked immunosorbent assay (ELISA)''' | ||
| + | |||
| + | We considered producing an ELISA to detect L-forms. One method would be to generate antibodies against a L-form specific antigen. Alternatively we considered introducing a novel gene into L-forms to result in a novel antigen being produced for us to generate antibodies against. However this would have involved using animals to generate polyclonal antibodies. We decided this raised ethical issues and was too time consuming to complete in our ten week placement. | ||
| + | |||
| + | ===References=== | ||
| + | Tsomlexoglou, E., Daulagala, P.W.H.K.P., Gooday, G.W., Glover, L.A., Seddon, B. and Allan, E.J. (2003) 'Molecular detection and β-glucuronidase expression of gus-marked Bacillus subtilis L-form bacteria in developing Chinese cabbage seedlings', Journal of Applied Microbiology, 95(2), pp. 218-224. | ||
| + | |||
| + | Ferguson, C.M.J., Booth, N.A. and Allan, E.J. (2000) 'An ELISA for the detection of Bacillus subtilis L-form bacteria confirms their symbiosis in strawberry', Letters in Applied Microbiology, 31(5), pp. 390-394. | ||
Latest revision as of 14:37, 14 June 2013
Contents |
Introducing and detecting L-forms in Plants
Detecting L-forms in Plants Using gusA Reporter Gene
Transformation B.subtilis to contain gusA
1) Transform L-forms of B. subtilis NCIMB8054.
2) Transformed L-forms will be selected by antibiotic resistance.
3) Conduct southern hybridization to confirm the integration of the gusA gene.
Production of L-form containing Plants
1) Wash seeds.
2) Grow seeds in petri dishes.
3) Incubate until radicals had just emerge.
4) Wash seeds with transformed L-forms.
5) Wash plants with deionised water to lyse extracellular L-forms.
6) Incubate plants.
Visualisation of L-forms in plants
1) Heat seeds in a vacuum oven with GUS staining solution.
2) Incubate at 37 degrees.
3) When glucuronidase activity appears, fix plants with formaldehyde.
Show gus gene is only present in transformed L-forms
1) Extract DNA from transformed L-form B. subtilis, L-form control and non L-form B.subtilis.
2) PCR: Use primers specific for gusA gene in a PCR to show gus A gene is present in transformed L-forms only.
Re-isolation of L-forms from seeds
1) Wash seeds treated with L-form bacteria or mannitol control with distilled water to remove any L-forms on the plant surface.
2) Place seeds in in mannitol solution.
3) Macerate seeds with pestle.
4) Plate out 100ul of suspension onto L-phase medium (which is designed for the growth of L-forms) and nutrient agar and incubate (also repeat using 100ul of original bacterial suspension on each of agar).
5) Look for signs of life, L-form or otherwise.
GusA Reporter Gene
Gus A reporter gene encodes beta-glucornide (GUS) an enzyme in Escherichia coli. BioBrick Part: BBa_K330002 [http://partsregistry.org/Part:BBa_K330002:Experience]
Detecting L-forms in Plants Using Red Flourescent Protein (RFP)
Transformation B.subtilis to contain RFP gene
1) Transform L-forms of B. subtilis NCIMB8054.
2) Transformed L-forms will be selected by antibiotic resistance.
3) Conduct southern hybridization to confirm the integration of the RFP gene.
Production of L-form containing Plants
1) Wash seeds.
2) Grow seeds in petri dishes.
3) Incubate until radicals had just emerge.
4) Wash seeds with transformed L-forms.
5) Wash plants with distillled water to lyse extracellular L-forms.
6) Incubate plants.
Show RFP gene is only present in transformed L-forms
1) Extract DNA from transformed L-form B. subtilis, L-form control and non L-form B.subtilis.
2) PCR: Use primers specific for RFP gene in a PCR to show gus A gene is present in transformed L-forms only.
Re-isolation of L-forms from seeds
1) Wash seeds treated with L-form bacteria or mannitol control with distilled water to remove any L-forms on the plant surface.
2) Place seeds in in mannitol solution.
3) Macerate seeds with pestle.
4) Plate out 100ul of suspension onto L-phase medium and nutrient agar and incubate (also repeat using 100ul of original bacterial suspension for each agar).
5) Look for signs of life, L-form or otherwise.
Alternative Methods Considered
Enzyme-linked immunosorbent assay (ELISA)
We considered producing an ELISA to detect L-forms. One method would be to generate antibodies against a L-form specific antigen. Alternatively we considered introducing a novel gene into L-forms to result in a novel antigen being produced for us to generate antibodies against. However this would have involved using animals to generate polyclonal antibodies. We decided this raised ethical issues and was too time consuming to complete in our ten week placement.
References
Tsomlexoglou, E., Daulagala, P.W.H.K.P., Gooday, G.W., Glover, L.A., Seddon, B. and Allan, E.J. (2003) 'Molecular detection and β-glucuronidase expression of gus-marked Bacillus subtilis L-form bacteria in developing Chinese cabbage seedlings', Journal of Applied Microbiology, 95(2), pp. 218-224.
Ferguson, C.M.J., Booth, N.A. and Allan, E.J. (2000) 'An ELISA for the detection of Bacillus subtilis L-form bacteria confirms their symbiosis in strawberry', Letters in Applied Microbiology, 31(5), pp. 390-394.
