Acinetobacter baylyi ADP1 Genome Manipulations

Acinetobacter baylyi ADP1 Genome Manipulations

Overview

Overlap PCR Construct Generation

The Design of Overlap PCR Primers and Constructs

• Annealing temperatures should be calculated in Phusion polymerase reaction conditions (which have a higher salt content than typical Taq reactions). Use the following calculator for determining annealing temperatures: https://www.neb.com/tools-and-resources/interactive-tools/tm-calculator
• Each homologous overlap should be at least 20bp long as well as each non-homology adding primer.
• When designing the overlap (or homology adding) primer, calculate the annealing temperature of each side of the primer separately. For example, if you have a primer NNNNNNNNNNNNNNYYYYYYYYYYYYYY where the Ns are homologous to the 3' end of the tdk-kan cassette and the Ys are homologous to the 5' end of the 3' seg piece, use only the Ys when calculating the annealing temperature for the 3' seg construction.
• The annealing temperature primers for the 5' seg and 3' seg amplification (green and red arrows in the diagram) should be within 2 degrees of each other - generally a Phusion Tm of approximately 62C is sought.
• Check the homologous overlap regions for hairpin formation using http://www.idtdna.com/analyzer/applications/oligoanalyzer/ . Stable hairpins at or above reaction annealing conditions will inhibit the overlap reaction.

For the design of the constructs themselves, flanking regions should be 500-1000bp long to facilitate efficient transformation into the ADP1 genome. We generally use 1kb on each side to obtain a high efficiency of transformation.

Overlap PCR Reactions

Initial PCR of 5' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM Tdk-kan to 5' seg RV primer
• ~10ng wild-type ADP1 gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation (the literature suggests 15-30 seconds per kb, but I tend to overshoot elongation times), and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Initial PCR of tdk-kan Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM tdk-kan FW primer
• 2.5uL 10uM tdk-kan RV primer
• ~10ng ADP1 Knock out collection clone gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 1 minute 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Initial PCR of 3' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM Tdk-kan to 3' seg FW primer
• 2.5uL 10uM +1kb RV primer
• ~10ng wild-type ADP1 gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Overlap PCR Reaction

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• ~30ng 5'seg PCR
• ~30ng tdk-kan PCR
• ~30ng 3'seg PCR
• 0.3uL Phusion polymerase
• dH2O to 45uL

Run this reaction in a standard Phusion PCR protocol with an annealing temperature of 60C, 2:30 elongation, and 15 repetitions. After the reaction is complete add:

• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM +1kb RV primer

Run this reaction for another 15 cycles with the appropriate annealing temperature. Once complete, run a 5uL aliquot of the reaction on a gel to check for the assembly of your 3.8kb product. This product is ready for transformation into ADP1.

Constructing Gene Knockouts (or interruptions) in A. baylyi ADP1

1. Identify the region in which you would like to insert the tdk-kan cassette.
2. Design and assemble your overlap construct (see above) such that homologous recombination with the genome will insert the construct at your desired location. One can either interrupt via insertion or replace the targeted gene to create a functional knock out.
3. Transform wild-type ADP1 with your reserved 45uL of overlap assembly PCR as per our standard transformation protocol. Allow to grow at 30C overnight in a shaking incubator. Be sure to include a no-DNA transformation control.
4. Plate both 100uL of undiluted and 100uL of a 1:100 dilution transformation onto dry LB-kan plates. Additionally, plate 100uL of undiluted control bacteria also onto a LB-kan plate. 1:1,000,000 dilutions for each reaction should also be plated on LB plates to allow transformation frequency to be calculated. Allow the plates to grow overnight in a 30C incubator.
5. Pick 3 colonies from one of the transformation plates into 5mL liquid LB+kan each and allow to grow to confluence.
6. Test each culture for the insertion via PCR and make a glycerol stock of successful insertions. PCR can be performed directly from the culture by diluting 1uL of culture into 1mL sterile dH2O and using 1uL of this as a PCR template. In the PCR reaction, the first 98C denaturing step should be changed from 30 seconds to 10 minutes to facilitate liberation of genomic DNA template.
   

Constructing Allelic Replacements

1. Follow the above protocol for knocking out your gene of interest, making sure to replace the entirety of the region you wish to exchange. Use of clones from the ADP1 knockout collection is encouraged.
2. Amplify the mutant allele of your choosing from the allele containing ADP1 strain. Add 500-1000bp of flanking homology on each side of the region of interest.
3. Transform the recipient strain using the amplified PCR product containing the mutant allele. Be sure to include a no DNA transformation control.
4. Plate the transformation on LB + 200ug/mL AZT plates (both undiluted and a 1:100 dilution). Allow to grow overnight at 30C.
5. Pick 3 colonies from the LB-AZT plates, inoculate into 5mL sterile LB and grow to confluence in a 30C shaking incubator.
6. Assay for the loss of the tdk-kan cassette via PCR using the confluent culture (see above for specifics). Glycerol stock successful rescues.
   

Constructing Insertions

Using a modified allelic exchange procedure, genetic constructs can be added to the ADP1 genome without the need to maintain a selective marker.

• In the construction of the tdk-kan integrated strain, target the cassette to the area where you would like to perform the insertion. It is not necessary to swap out a region of the genome with the cassette.
• Rescue the tdk-kan insertion with with sequence you wish to insert.

Contributors

Acinetobacter baylyi ADP1 Genome Manipulations

Overview

Genome manipulations in Acinetobacter baylyi ADP1 can be performed without the need for exogenous recombinase expression, plasmid electroporation, or other practices used in other canonical systems such as E. coli. With just the transformation of PCR products, one can make gene knockouts, insertions, allelic replacement, and deletions. The listed protocols use the tdk-kan selection/counter selection cassette as retrieved from the ADP1 single gene knockout project, but other selection/counter-selection cassettes (such as kan-sacB) may also be used. Our general strategy is to first construct our transforming constructs with targeted homology to the genome using a 3 piece overlap PCR and then (for all procedures minus simple knock outs) rescuing the insertion of that cassette into the genome with the desired construct using the tdk counter-selection.

Overlap PCR Construct Generation

The Design of Overlap PCR Primers and Constructs

In order to ensure a successful assembly of transforming constructs, particular care should be made when designing the appropriate primers. A total of 6 primers are needed (see Initial PCRs panel in the provided figure), two of which will add homology of the tdk-kan cassette to the upstream flanking region (5' seg) and downstream flanking region (3' seg). The following guidelines for primer construction should be followed:

• Annealing temperatures should be calculated in Phusion polymerase reaction conditions (which have a higher salt content than typical Taq reactions). Use the following calculator for determining annealing temperatures: https://www.neb.com/tools-and-resources/interactive-tools/tm-calculator
• Each homologous overlap should be at least 20bp long as well as each non-homology adding primer.
• When designing the overlap (or homology adding) primer, calculate the annealing temperature of each side of the primer separately. For example, if you have a primer NNNNNNNNNNNNNNYYYYYYYYYYYYYY where the Ns are homologous to the 3' end of the tdk-kan cassette and the Ys are homologous to the 5' end of the 3' seg piece, use only the Ys when calculating the annealing temperature for the 3' seg construction.
• The annealing temperature primers for the 5' seg and 3' seg amplification (green and red arrows in the diagram) should be within 2 degrees of each other - generally a Phusion Tm of approximately 62C is sought.
• Check the homologous overlap regions for hairpin formation using http://www.idtdna.com/analyzer/applications/oligoanalyzer/ . Stable hairpins at or above reaction annealing conditions will inhibit the overlap reaction.

For the design of the constructs themselves, flanking regions should be 500-1000bp long to facilitate efficient transformation into the ADP1 genome. We generally use 1kb on each side to obtain a high efficiency of transformation.

Overlap PCR Reactions

Initial PCR of 5' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM Tdk-kan to 5' seg RV primer
• ~10ng wild-type ADP1 gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation (the literature suggests 15-30 seconds per kb, but I tend to overshoot elongation times), and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Initial PCR of tdk-kan Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM tdk-kan FW primer
• 2.5uL 10uM tdk-kan RV primer
• ~10ng ADP1 Knock out collection clone gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 1 minute 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Initial PCR of 3' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM Tdk-kan to 3' seg FW primer
• 2.5uL 10uM +1kb RV primer
• ~10ng wild-type ADP1 gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Overlap PCR Reaction

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• ~30ng 5'seg PCR
• ~30ng tdk-kan PCR
• ~30ng 3'seg PCR
• 0.3uL Phusion polymerase
• dH2O to 45uL

Run this reaction in a standard Phusion PCR protocol with an annealing temperature of 60C, 2:30 elongation, and 15 repetitions. After the reaction is complete add:

• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM +1kb RV primer

Run this reaction for another 15 cycles with the appropriate annealing temperature. Once complete, run a 5uL aliquot of the reaction on a gel to check for the assembly of your 3.8kb product. This product is ready for transformation into ADP1.

Constructing Gene Knockouts (or interruptions) in A. baylyi ADP1

1. Identify the region in which you would like to insert the tdk-kan cassette.
2. Design and assemble your overlap construct (see above) such that homologous recombination with the genome will insert the construct at your desired location. One can either interrupt via insertion or replace the targeted gene to create a functional knock out.
3. Transform wild-type ADP1 with your reserved 45uL of overlap assembly PCR as per our standard transformation protocol. Allow to grow at 30C overnight in a shaking incubator. Be sure to include a no-DNA transformation control.
4. Plate both 100uL of undiluted and 100uL of a 1:100 dilution transformation onto dry LB-kan plates. Additionally, plate 100uL of undiluted control bacteria also onto a LB-kan plate. 1:1,000,000 dilutions for each reaction should also be plated on LB plates to allow transformation frequency to be calculated. Allow the plates to grow overnight in a 30C incubator.
5. Pick 3 colonies from one of the transformation plates into 5mL liquid LB+kan each and allow to grow to confluence.
6. Test each culture for the insertion via PCR and make a glycerol stock of successful insertions. PCR can be performed directly from the culture by diluting 1uL of culture into 1mL sterile dH2O and using 1uL of this as a PCR template. In the PCR reaction, the first 98C denaturing step should be changed from 30 seconds to 10 minutes to facilitate liberation of genomic DNA template.
   

Constructing Allelic Replacements

1. Follow the above protocol for knocking out your gene of interest, making sure to replace the entirety of the region you wish to exchange. Use of clones from the ADP1 knockout collection is encouraged.
2. Amplify the mutant allele of your choosing from the allele containing ADP1 strain. Add 500-1000bp of flanking homology on each side of the region of interest.
3. Transform the recipient strain using the amplified PCR product containing the mutant allele. Be sure to include a no DNA transformation control.
4. Plate the transformation on LB + 200ug/mL AZT plates (both undiluted and a 1:100 dilution). Allow to grow overnight at 30C.
5. Pick 3 colonies from the LB-AZT plates, inoculate into 5mL sterile LB and grow to confluence in a 30C shaking incubator.
6. Assay for the loss of the tdk-kan cassette via PCR using the confluent culture (see above for specifics). Glycerol stock successful rescues.
   

Constructing Insertions

Using a modified allelic exchange procedure, genetic constructs can be added to the ADP1 genome without the need to maintain a selective marker.

• In the construction of the tdk-kan integrated strain, target the cassette to the area where you would like to perform the insertion. It is not necessary to swap out a region of the genome with the cassette.
• Rescue the tdk-kan insertion with with sequence you wish to insert.

Acinetobacter baylyi ADP1 Genome Manipulations

Overview

Genome manipulations in Acinetobacter baylyi ADP1 can be performed without the need for exogenous recombinase expression, plasmid electroporation, or other practices used in other canonical systems such as E. coli. With just the transformation of PCR products, one can make gene knockouts, insertions, allelic replacement, and deletions. The listed protocols use the tdk-kan selection/counter selection cassette as retrieved from the ADP1 single gene knockout project, but other selection/counter-selection cassettes (such as kan-sacB) may also be used. Our general strategy is to first construct our transforming constructs with targeted homology to the genome using a 3 piece overlap PCR and then (for all procedures minus simple knock outs) rescuing the insertion of that cassette into the genome with the desired construct using the tdk counter-selection.

Overlap PCR Construct Generation

The Design of Overlap PCR Primers and Constructs

In order to ensure a successful assembly of transforming constructs, particular care should be made when designing the appropriate primers. A total of 6 primers are needed (see Initial PCRs panel in the provided figure), two of which will add homology of the tdk-kan cassette to the upstream flanking region (5' seg) and downstream flanking region (3' seg). The following guidelines for primer construction should be followed:

• Annealing temperatures should be calculated in Phusion polymerase reaction conditions (which have a higher salt content than typical Taq reactions). Use the following calculator for determining annealing temperatures: https://www.neb.com/tools-and-resources/interactive-tools/tm-calculator
• Each homologous overlap should be at least 20bp long as well as each non-homology adding primer.
• When designing the overlap (or homology adding) primer, calculate the annealing temperature of each side of the primer separately. For example, if you have a primer NNNNNNNNNNNNNNYYYYYYYYYYYYYY where the Ns are homologous to the 3' end of the tdk-kan cassette and the Ys are homologous to the 5' end of the 3' seg piece, use only the Ys when calculating the annealing temperature for the 3' seg construction.
• The annealing temperature primers for the 5' seg and 3' seg amplification (green and red arrows in the diagram) should be within 2 degrees of each other - generally a Phusion Tm of approximately 62C is sought.
• Check the homologous overlap regions for hairpin formation using http://www.idtdna.com/analyzer/applications/oligoanalyzer/ . Stable hairpins at or above reaction annealing conditions will inhibit the overlap reaction.

For the design of the constructs themselves, flanking regions should be 500-1000bp long to facilitate efficient transformation into the ADP1 genome. We generally use 1kb on each side to obtain a high efficiency of transformation.

Overlap PCR Reactions

Initial PCR of 5' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM Tdk-kan to 5' seg RV primer
• ~10ng wild-type ADP1 gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation (the literature suggests 15-30 seconds per kb, but I tend to overshoot elongation times), and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Initial PCR of tdk-kan Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM tdk-kan FW primer
• 2.5uL 10uM tdk-kan RV primer
• ~10ng ADP1 Knock out collection clone gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 1 minute 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Initial PCR of 3' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM Tdk-kan to 3' seg FW primer
• 2.5uL 10uM +1kb RV primer
• ~10ng wild-type ADP1 gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background ADP1 genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Overlap PCR Reaction

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• ~30ng 5'seg PCR
• ~30ng tdk-kan PCR
• ~30ng 3'seg PCR
• 0.3uL Phusion polymerase
• dH2O to 45uL

Run this reaction in a standard Phusion PCR protocol with an annealing temperature of 60C, 2:30 elongation, and 15 repetitions. After the reaction is complete add:

• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM +1kb RV primer

Run this reaction for another 15 cycles with the appropriate annealing temperature. Once complete, run a 5uL aliquot of the reaction on a gel to check for the assembly of your 3.8kb product. This product is ready for transformation into ADP1.

Constructing Gene Knockouts (or interruptions) in A. baylyi ADP1

1. Identify the region in which you would like to insert the tdk-kan cassette.
2. Design and assemble your overlap construct (see above) such that homologous recombination with the genome will insert the construct at your desired location. One can either interrupt via insertion or replace the targeted gene to create a functional knock out.
3. Transform wild-type ADP1 with your reserved 45uL of overlap assembly PCR as per our standard transformation protocol. Allow to grow at 30C overnight in a shaking incubator. Be sure to include a no-DNA transformation control.
4. Plate both 100uL of undiluted and 100uL of a 1:100 dilution transformation onto dry LB-kan plates. Additionally, plate 100uL of undiluted control bacteria also onto a LB-kan plate. 1:1,000,000 dilutions for each reaction should also be plated on LB plates to allow transformation frequency to be calculated. Allow the plates to grow overnight in a 30C incubator.
5. Pick 3 colonies from one of the transformation plates into 5mL liquid LB+kan each and allow to grow to confluence.
6. Test each culture for the insertion via PCR and make a glycerol stock of successful insertions. PCR can be performed directly from the culture by diluting 1uL of culture into 1mL sterile dH2O and using 1uL of this as a PCR template. In the PCR reaction, the first 98C denaturing step should be changed from 30 seconds to 10 minutes to facilitate liberation of genomic DNA template.
   

Constructing Allelic Replacements

1. Follow the above protocol for knocking out your gene of interest, making sure to replace the entirety of the region you wish to exchange. Use of clones from the ADP1 knockout collection is encouraged.
2. Amplify the mutant allele of your choosing from the allele containing ADP1 strain. Add 500-1000bp of flanking homology on each side of the region of interest.
3. Transform the recipient strain using the amplified PCR product containing the mutant allele. Be sure to include a no DNA transformation control.
4. Plate the transformation on LB + 200ug/mL AZT plates (both undiluted and a 1:100 dilution). Allow to grow overnight at 30C.
5. Pick 3 colonies from the LB-AZT plates, inoculate into 5mL sterile LB and grow to confluence in a 30C shaking incubator.
6. Assay for the loss of the tdk-kan cassette via PCR using the confluent culture (see above for specifics). Glycerol stock successful rescues.
   

Constructing Insertions

Using a modified allelic exchange procedure, genetic constructs can be added to the ADP1 genome without the need to maintain a selective marker.

• In the construction of the tdk-kan integrated strain, target the cassette to the area where you would like to perform the insertion. It is not necessary to swap out a region of the genome with the cassette.
• Rescue the tdk-kan insertion with with sequence you wish to insert.

-- Main.BrianRenda - 13 Jun 2013

Overview

Overlap PCR Construct Generation

The Design of Overlap PCR Primers and Constructs

In order to ensure a successful assembly of transforming constructs, particular care should be made when designing the appropriate primers. A total of 6 primers are needed (see Initial PCRs panel in the provided figure), two of which will add homology of the tdk-kan cassette to the upstream flanking region (5' seg) and downstream flanking region (3' seg). The following guidelines for primer construction should be followed:

• Annealing temperatures should be calculated in Phusion polymerase reaction conditions (which have a higher salt content than typical Taq reactions). Use the following calculator for determining annealing temperatures: https://www.neb.com/tools-and-resources/interactive-tools/tm-calculator
• Each homologous overlap should be at least 20bp long as well as each non-homology adding primer.

• Check the homologous overlap regions for hairpin formation using http://www.idtdna.com/analyzer/applications/oligoanalyzer/ . Stable hairpins at or above reaction annealing conditions will inhibit the overlap reaction.

Overlap PCR Reactions

Initial PCR of 5' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM Tdk-kan to 5' seg RV primer

• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation (the literature suggests 15-30 seconds per kb, but I tend to overshoot elongation times), and 29 repetitions.

Initial PCR of tdk-kan Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM tdk-kan FW primer
• 2.5uL 10uM tdk-kan RV primer

• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 1 minute 72C elongation, and 29 repetitions.

Initial PCR of 3' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM Tdk-kan to 3' seg FW primer
• 2.5uL 10uM +1kb RV primer

• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation, and 29 repetitions.

Overlap PCR Reaction

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• ~30ng 5'seg PCR
• ~30ng tdk-kan PCR
• ~30ng 3'seg PCR
• 0.3uL Phusion polymerase
• dH2O to 45uL

Run this reaction in a standard Phusion PCR protocol with an annealing temperature of 60C, 2:30 elongation, and 15 repetitions. After the reaction is complete add:

• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM +1kb RV primer

1. Identify the region in which you would like to insert the tdk-kan cassette.
2. Design and assemble your overlap construct (see above) such that homologous recombination with the genome will insert the construct at your desired location. One can either interrupt via insertion or replace the targeted gene to create a functional knock out.

1. Plate both 100uL of undiluted and 100uL of a 1:100 dilution transformation onto dry LB-kan plates. Additionally, plate 100uL of undiluted control bacteria also onto a LB-kan plate. 1:1,000,000 dilutions for each reaction should also be plated on LB plates to allow transformation frequency to be calculated. Allow the plates to grow overnight in a 30C incubator.
2. Pick 3 colonies from one of the transformation plates into 5mL liquid LB+kan each and allow to grow to confluence.
3. Test each culture for the insertion via PCR and make a glycerol stock of successful insertions. PCR can be performed directly from the culture by diluting 1uL of culture into 1mL sterile dH2O and using 1uL of this as a PCR template. In the PCR reaction, the first 98C denaturing step should be changed from 30 seconds to 10 minutes to facilitate liberation of genomic DNA template.
   

Constructing Allelic Replacements

1. Transform the recipient strain using the amplified PCR product containing the mutant allele. Be sure to include a no DNA transformation control.
2. Plate the transformation on LB + 200ug/mL AZT plates (both undiluted and a 1:100 dilution). Allow to grow overnight at 30C.
3. Pick 3 colonies from the LB-AZT plates, inoculate into 5mL sterile LB and grow to confluence in a 30C shaking incubator.
4. Assay for the loss of the tdk-kan cassette via PCR using the confluent culture (see above for specifics). Glycerol stock successful rescues.
   

Constructing Insertions

• In the construction of the tdk-kan integrated strain, target the cassette to the area where you would like to perform the insertion. It is not necessary to swap out a region of the genome with the cassette.
• Rescue the tdk-kan insertion with with sequence you wish to insert.

-- Main.BrianRenda - 13 Jun 2013

Acinetobacter baylyi ADP1 Genome Manipulations

Overview

Genome manipulations in Acinetobacter baylyi ADP1 (AB) can be performed without the need for exogenous recombinase expression, plasmid electroporation, or other practices used in other canonical systems such as E. coli. With just the transformation of PCR products, one can make gene knockouts, insertions, allelic replacement, and deletions. The listed protocols use the tdk-kan selection/counter selection cassette as retrieved from the AB single gene knockout project, but other selection/counter-selection cassettes (such as kan-sacB) may also be used. Our general strategy is to first construct our transforming constructs with targeted homology to the genome using a 3 piece overlap PCR and then (for all procedures minus simple knock outs) rescuing the insertion of that cassette into the genome with the desired construct using the tdk counter-selection.

Overlap PCR Construct Generation

The Design of Overlap PCR Primers and Constructs

In order to ensure a successful assembly of transforming constructs, particular care should be made when designing the appropriate primers. A total of 6 primers are needed (see Initial PCRs panel in the provided figure), two of which will add homology of the tdk-kan cassette to the upstream flanking region (5' seg) and downstream flanking region (3' seg). The following guidelines for primer construction should be followed:

• Annealing temperatures should be calculated in Phusion polymerase reaction conditions (which have a higher salt content than typical Taq reactions). Use the following calculator for determining annealing temperatures: https://www.neb.com/tools-and-resources/interactive-tools/tm-calculator
• Each homologous overlap should be at least 20bp long as well as each non-homology adding primer.
• When designing the overlap (or homology adding) primer, calculate the annealing temperature of each side of the primer separately. For example, if you have a primer NNNNNNNNNNNNNNYYYYYYYYYYYYYY where the Ns are homologous to the 3' end of the tdk-kan cassettee and the Ys are homologous to the 5' end of the 3'seg piece, use only the Ys when calculating the annealing temperature for the 3'seg construction.
• The annealing temperature primers for the 5'seg and 3' seg amplification (green and red arrows in the diagram) should be within 2 degrees of each other - generally a Phusion Tm of approximately 62C is sought.
• Check the homologous overlap regions for hairpin formation using http://www.idtdna.com/analyzer/applications/oligoanalyzer/ . Stable hairpins at or above reaction annealing conditions will inhibit the overlap reaction.

Overlap PCR Reactions

Initial PCR of 5' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM Tdk-kan to 5' seg RV primer
• ~10ng wild-type AB gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Initial PCR of tdk-kan Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM tdk-kan FW primer
• 2.5uL 10uM tdk-kan RV primer
• ~10ng AB Knock out collection clone gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 1 minute 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background AB genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Initial PCR of 3' Segment

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• 2.5uL 10uM Tdk-kan to 3' seg FW primer
• 2.5uL 10uM +1kb RV primer
• ~10ng wild-type AB gDNA
• 0.3uL Phusion polymerase
• dH2O to 50uL

Run with a standard phusion PCR protocol with the appropriate annealing temperature, 45 second 72C elongation, and 29 repetitions.

After the reaction, add 1uL of 20,000U/mL Dpn1 restriction enzyme and incubate at 37C for 1 hour. This will digest any background AB genomic DNA template. Once the digestion is completed, run a 5uL aliquot of the reaction on an agarose gel to check for product formation and purify the remaining 45uL reaction with a PCR cleanup kit. Do not elute in buffer containing EDTA. Quantify the DNA concentration and keep in the freezer until ready to perform the overlap PCR.

Overlap PCR Reaction

• 10uL 5X Phusion HF Buffer
• 1uL dNTP stock
• ~30ng 5'seg PCR
• ~30ng tdk-kan PCR
• ~30ng 3'seg PCR
• 0.3uL Phusion polymerase
• dH2O to 45uL

Run this reaction in a standard Phusion PCR protocol with an annealing temperature of 60C, 2:30 elongation, and 15 repetitions. After the reaction is complete add:

• 2.5uL 10uM +1kb FW primer
• 2.5uL 10uM +1kb RV primer

Run this reaction for another 15 cycles with the appropriate annealing temperature. Once complete, run a 5uL aliquot of the reaction on a gel to check for the assembly of your 3.8kb product. This product is ready for transformation into AB.

Constructing Gene Knockouts (or interruptions) in A. baylyi ADP1

1. Identify the region in which you would like to insert the tdk-kan cassette.
2. Design and assemble your overlap construct (see above) such that homologous recombination with the genome will insert the construct at your desired location. One can either interrupt via insertion or replace the targeted gene to create a functional knock out.
3. Transform wild-type AB with your reserved 45uL of overlap assembly PCR as per our standard transformation protocol. Allow to grow at 30C overnight in a shaking incubator. Be sure to include a no-DNA transformation control.
4. Plate both 100uL of undiluted and 100uL of a 1:100 dilution transformation onto dry LB-kan plates. Additionally, plate 100uL of undiluted control bacteria also onto a LB-kan plate. 1:1,000,000 dilutions for each reaction should also be plated on LB plates to allow transformation frequency to be calculated. Allow the plates to grow overnight in a 30C incubator.
5. Pick 3 colonies from one of the transformation plates into 5mL liquid LB+kan each and allow to grow to confluence.
6. Test each culture for the insertion via PCR and make a glycerol stock of successful insertions. PCR can be performed directly from the culture by diluting 1uL of culture into 1mL sterile dH2O and using 1uL of this as a PCR template. In the PCR reaction, the first 98C denaturing step should be changed from 30 seconds to 10 minutes to facilitate liberation of genomic DNA template.
   

Constructing Allelic Replacements

1. Follow the above protocol for knocking out your gene of interest, making sure to replace the entirety of the region you wish to exchange. Use of clones from the AB knockout collection is encouraged.
2. Amplify the mutant allele of your choosing from the allele containing AB strain. Add 500-1000bp of flanking homology on each side of the region of interest.
3. Transform the recipient strain using the amplified PCR product containing the mutant allele. Be sure to include a no DNA transformation control.
4. Plate the transformation on LB + 200ug/mL AZT plates (both undiluted and a 1:100 dilution). Allow to grow overnight at 30C.
5. Pick 3 colonies from the LB-AZT plates, inoculate into 5mL sterile LB and grow to confluence in a 30C shaking incubator.
6. Assay for the loss of the tdk-kan cassette via PCR using the confluent culture (see above for specifics). Glycerol stock successful rescues.
   

Constructing Insertions

Using a modified allelic exchange procedure, genetic constructs can be added to the AB genome without the need to maintain a selective marker.

• In the construction of the tdk-kan integrated strain, target the cassette to the area where you would like to perform the insertion. It is not necessary to swap out a region of the genome with the cassette.
• Rescue the tdk-kan insertion with with sequence you wish to insert.

-- Main.BrianRenda - 13 Jun 2013

Overview

Genome manipulations in Acinetobacter baylyi ADP1 (AB) can be performed without the need for exogenous recombinase expression, plasmid electroporation, or other practices used in other canonical systems such as E. coli. With just the transformation of PCR products, one can make gene knockouts, insertions, allelic replacement, and deletions. The listed protocols use the tdk-kan selection/counter selection cassette as retrieved from the AB single gene knockout project, but other selection/counter-selection cassettes (such as kan-sacB) may also be used. Our general strategy is to first construct our transforming constructs with targeted homology to the genome using a 3 piece overlap PCR and then (for all procedures minus simple knock outs) rescuing the insertion of that cassette into the genome with the desired construct using the tdk counter-selection.

Overlap PCR Construct Generation

The Design of Overlap PCR Primers and Constructs

Acinetobacter baylyi ADP1 Genome Manipulations - Note: Protocol Construction In Progress

Overview

Genome manipulations in Acinetobacter baylyi ADP1 (AB) can be performed without the need for exogenous recombinase expression, plasmid electroporation, or other practices used in other canonical systems such as E. coli. With just the transformation of PCR products, one can make gene knockouts, insertions, allelic replacement, and deletions. The listed protocols use the tdk-kan selection/counter selection cassette as retrieved from the AB single gene knockout project, but other selection/counter-selection cassettes (such as kan-sacB) may also be used. Our general strategy is to first construct our transforming constructs with targeted homology to the genome using a 3 piece overlap PCR and then (for all procedures minus simple knock outs) rescuing the insertion of that cassette into the genome with the desired construct using the tdk counter-selection.

Overlap PCR Construct Generation

The Design of Overlap PCR Primers and Constructs

In order to ensure a successful assembly of transforming constructs, particular care should be made when designing the appropriate primers.

Notes/Considerations in AB transformations

• to avoid the use wet plates or plates with abberant surface texture. Wet plates will haze individual colonies and abberant surface texture produces irregular morphologies.
• Linearized plasmid will not recircularize in an AB transformation unless two separate digestions with different cut sites on the plasmid are used. It is best to just transform whole plasmid.

-- Main.BrianRenda - 13 Jun 2013