Difference between revisions of "Team:NU Kazakhstan/Project"
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1. Sasaki, Y., Nogami, E., Maeda, M., Nakanishi-Matsui, M., & Iwamoto-Kihara, A. (2014). A unique F-type H+-ATPase from Streptococcus mutans: An active H+ pump at acidic pH. Biochemical and biophysical research communications, 443(2), 677-682. | 1. Sasaki, Y., Nogami, E., Maeda, M., Nakanishi-Matsui, M., & Iwamoto-Kihara, A. (2014). A unique F-type H+-ATPase from Streptococcus mutans: An active H+ pump at acidic pH. Biochemical and biophysical research communications, 443(2), 677-682. | ||
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Revision as of 06:02, 13 September 2015
Description
S. mutans (Gram+, Biosafety level 1, naturally competent cells) is an etiologic agent of dental caries which adheres to tooth surfaces and responsible for the biofilm formation known as dental plaque. Dietary sugars metabolized by S. mutans result in the production and secretion of lactic acid, which in turn reduces the pH of the dental cavity. S. mutans possess a membrane-bound F-ATPase that helps to survive them in acidic environment by pumping H+ ions out of the cell (Sasaki et al., 2014). S. mutans survival is tightly associated with the activation of quorum sensing mechanisms that are involved in growth proliferation and biofilm formation. Thus, the aim of this project is to design smart DNA plasmid constructs that will operate according to the following:
1. Will inhibit bacterial growth and biofilm formation through the action of XrpA protein controlled by the pH-sensitive promoter.
2. Will inhibit the VicK (putative histidine kinase) transcription via modified CRISPR-dCas9 complex, since Vick is involved in signal transduction for the activation of lactate metabolism in S. mutans.
In order to control the action of the plasmids, safety regulation mechanisms will be introduced to the system above. Plasmid will be eliminated by the blue-light activation. The safety mechanism ceases the functionality of the plasmid’s origin of the replication via CRISPR-dCas9 system, thus a further propagation of construct to the next generation is eliminated.
The two pathways for XrpA and VicK actions are shown below.
Experiments and Protocols
MAKING COMPETENT CELLS
1. Inoculate a single colony into 5 mL LB in 50 mL falcon tube (taped on a loosed tap). 2. Grow on 37°C with shaking for 130 rpm overnight. 3. Use 1 mL to inoculate 100 mL to inoculate 100 mL of LB in 250 mL bottle the next morning. 4. Shake 37°C for 1.5-3 hours. 5. When OD is between 0.3-0.4 at 600 nm wavelength put cell on ice. 6. Hold cells on ice for the 10 minutes. 7. Collect cells by centrifugation for 3 min at maximum speed (4700 rpm). 8. Decant supernatant and gently resuspend on 10 mL ice-cold 0.1 M CaCl2 (prepared in ddH2O). Treat them gently. 9. Incubate on ice for 20 minutes. 10. Centrifuge again at maximum speed (4700 rpm). 11. Discard supernatant and gently resuspend in 5 mL cold 0.1 M CaCl2 (15% glycerol). 12. Dispense into chilled microtubes, put on the dry ice. Perform this procedure very quickly. 13. Freeze in -80°C.
TRANSFORMATION
1. Start thawing the competent cells on ice. 2. Add 50 µL of thawed competent cells into pre-chilled 2ml tube, and another 50µL into a 2ml tube, labelled for your control. 3. Add 1 - 2 µL of the resuspended DNA to the 2ml tube. Pipet up and down a few times, gently. Make sure to keep the competent cells on ice. 4. Add 1 µL of the RFP Control to your control transformation. 5. Close tubes and incubate the cells on ice for 30 minutes. 6. Heat shock the cells by immersion in a pre-heated water bath at 42ºC for 60 seconds. 7. Incubate the cells on ice for 5 minutes. 8. Add 200 μl of SOC media (make sure that the broth does not contain antibiotics and is not contaminated) to each transformation 9. Incubate the cells at 37ºC for 2 hours while the tubes are rotating or shaking. Important: 2 hour recovery time helps in transformation efficiency, especially for plasmid backbones with antibiotic resistance other than ampicillin. 10. Label two petri dishes with LB agar and the appropriate antibiotic(s) with the part number, plasmid backbone, and antibiotic resistance. Plate 20 µl and 200 µl of the transformation onto the dishes, and spread. This helps ensure that you will be able to pick out a single colony. 11. For the control, label two petri dishes with LB agar (AMP). Plate 20 µl and 200 µl of the transformation onto the dishes, and spread. 12. Incubate the plates at 37ºC for 12-14 hours, making sure the agar side of the plate is up. If incubated for too long the antibiotics start to break down and un-transformed cells will begin to grow. This is especially true for ampicillin - because the resistance enzyme is excreted by the bacteria, and inactivates the antibiotic outside of the bacteria. 13. You can pick a single colony, make a glycerol stock, grow up a cell culture and miniprep. 14. Count the colonies on the 20 μl control plate and calculate your competent cell efficiency.
LIGATION
1. Add 2ul of digested plasmid backbone (25 ng) 2. Add equimolar amount of EcoRI-HF SpeI digested fragment (< 3 ul) 3. Add equimolar amount of XbaI PstI digested fragment (< 3 ul) 4. Add 1 ul T4 DNA ligase buffer. Note: Do not use quick ligase 5. Add 0.5 ul T4 DNA ligase 6. Add water to 10 ul 7. Ligate 16C/30 min, heat kill 80C/20 min 8. Transform with 1-2 ul of product
DNA EXTRACTION FROM CELLS (MINIPREP)
1. Harvest. Centrifuge 1-5 mL of the overnight LB-culture (Use 1-2×104 E.coli cells for each sample). Remove all medium. Add 2 mL of ddH2O and centrifuge again. Remove all medium. 2. Resuspend. Add 250 uL Resuspension Buffer (R3) with RNase A to the cell pellet and resuspend the pellet until it is homogenous. 3. Lyse. Add 250 uL Lysis Buffer (L7). Mix gently by inverting the capped tube until the mixture is homogenous. Do not vortex. Incubate the tube at room temperature for 5 minutes. 4. Precipitate. Add 350 uL Precipitation Buffer (N4). Mix immediately by inverting the tube, or for large pellets, vigorously shaking the tube, until the mixture is homogenous. Do not vortex. Centrifuge the lysate at >12,000 g for 10 minutes. 5. Bind. Load the supernatant from step 4 onto a spin column in a 2-mL wash tube. Centrifuge the column at 12,000 g for 1 minute. Discard the flow-through and place the column back into the wash tube. 6. Optional wash (Recommended for endA+ strains). Add 500 uL Wash Buffer (W10) with ethanol to the column. Incubate the column for 1 minute at room temperature. Centrifuge the column at 12,000 g for 1 minute. Discard the flow-through and place the column back into the wash tube. 7. Wash and remove ethanol. Add 700 uL Wash Buffer (W9) with ethanol to the column. Centrifuge the column at 12,000 g for 1 minute. Discard the flow-through and place the column back into the wash tube. Centrifuge the column at 12,000 g for 1 minute. Discard the flow-through. 8. Elute. Place the Spin Column in a clean 1.5-mL recovery tube. Add 75 uL of preheated TE Buffer (TE) to the center of the column. Incubate the column for 1 minute at room temperature. 9. Recover. Centrifuge the column at 12,000 g for 2 minutes. The recovery tube contains the purified plasmid DNA at 4⁰C (short-term) or store DNA in aliquots at -20⁰C (long-term).
DNA EXTRACTION FROM GEL
Excising and dissolving the gel
1. Equilibrate a water bath or heat block to 50⁰C. 2. Excise a minimal area of gel containing the DNA fragment of interest. 3. Weigh the gel slice containing the DNA fragment using a scale sensitive to 0.001 g. 4. Add Gel Solubilization Buffer (L3) to the excised gel in the tube size indicated in the following table: Gel Tube Buffer L3 Volume ≤2% agarose 1.7-mL polypropylene 3:1 (i.e. 1.2 mL Buffer L3 : 400 mg gel piece) >2% agarose 5-mL polypropylene 6:1 (i.e. 2.4 mL Buffer L3 : 400 mg gel piece) 5. Place the tube with the gel slice and Buffer L3 into a 50⁰C water bath or heat block. Incubate the tube at 50⁰C for 10 minutes. Invert the tube every 3 minutes to mix and ensure gel dissolution. 6. After the gel slice appears dissolved, incubate the tube for an additional 5 minutes. 7. Optional: For optimal DNA yields, add 1 gel volume of isopropanol to the dissolved gel slice. Mix well. 8. Purify the DNA using a centrifuge.
Purifying DNA using a centrifuge
1. Load. Pipet the dissolved gel piece onto a Quick Gel Extraction Column inside a Wash Tube. Use 1 column per 400 mg of agarose gel. Note: the column reservoir capacity is 850 uL. 2. Bind. Centrifuge the column at >12,000 g for 1 minute. Discard the flow-through and place the column into the Wash Tube. 3. Wash. Add 50 uL Wash Buffer (W1) containing ethanol to the column. 4. Remove Buffer. Centrifuge the column at >12,000 g for 1 minute. Discard the flow-through and place the column into the Wash Tube. Repeat Steps 3 and 4. 5. Remove Ethanol. Centrifuge the column at maximum speed for 3 minutes. Discard the flow-through. 6. Elute. Place the column into a Recovery Tube. Add 50 uL Elution Buffer (E5) to the center of the column. Incubate the tube for 2 minutes at room temperature. 7. Collect. Centrifuge the tube at >12,000 g for 5 minutes. 8. Store. The elution tube contains the purified DNA. Store the purified DNA at 4⁰C for immediate use or at -20⁰C for long-term storage.
DNA ISOLATION FROM BACTERIA
1. Pick an isolated bacterial colony and resuspend it in 1 mL of autoclaved water in a microfuge tube. 2. Centrifuge for 1 minute at 10,000-12,000 rpm. Remove the supernatant. 3. Add 200 uL of InstaGene matrix to the pellet and incubate at 56⁰c for 15-30 minutes. Note: InstaGene matrix should be mixed at moderate speed on a magnetic stirrer to maintain the matrix in suspension. The pipet tip used should have a large bore, such as 1,000 uL pipet tip 4. Vortex at high speed for 10 seconds. Place the tube in a 100⁰C heat block or boiling water bath for 8 minutes. 5. Vortex at high speed for 10 seconds. Spin at 10,000-12,000 rpm for 2-3 minutes. 6. Use 20 uL of the resulting supernatant per 50 uL PCR reaction. Store the remainder of the supernatant at -20⁰C. Repeat Step 5 when reusing the InstaGene preparation. Note: It is important to store the prepared sample at -20⁰C.