(r37) ProtocolsAcinetobacterGoldenTransformation < Lab

---+ _Acinetobacter baylyi_ ADP1 Golden Transformation

---++ Overview

The following protocol is to be used as a substitute for overlap extension PCR for constructing double-stranded DNA fragments that template sequence replacements and/or deletions in the ADP1 genome. Addition of the flanking sequence homology needed for efficient transformation is based on Golden Gate Assembly and is much simpler and less time consuming to perform.

Fundamentally, [[http://www.ncbi.nlm.nih.gov/pubmed/25871405][Golden Gate Assembly/cloning]] involves the use of plasmids which contain defined parts, called &ldquo;part plasmids&rdquo;, that when cut with BsaI enzymes and re-ligated (using the Golden Gate Reaction reagents and thermocycler protocol), allow the assembly of multiple parts in the desired order into a new plasmid. All of this is achieved in a single reaction tube, and then the unpurified reaction mix can be used to transform competent cells.

Here we use a two-step protocol to edit the ADP1 genome. In the first step we use Golden Gate assembly to add flanking homology to the positive/negitive selection cassette (tdk/kan) we routinely use for ADP1 transformations and insert it into the genome. This reaction requires only three DNA parts: <br />A- pBTK622-tdkkan-camR plasmid <br />B- Purified PCR product of 5&rsquo;-flank homology (~1kb) <br />C- Purified PCR product of 3&rsquo;-flank homology (~1kb) </br>
<b>Figure 1</b> The three reaction components</br>
<img width="200" alt="Figure_GoldenGateTransformation.JPG" src="%ATTACHURLPATH%/Figure_GoldenGateTransformation.JPG" height="250" /></br>

The insertion of the tdk/kan cassette is selected for on kanamycin antibiotic plates. In the second step the insertion of this cassette is "rescued" by recombination with either a deletion or insertion substrate DNA and counter-selected for the loss of the _tdk_ counter selectable marker.

Note: pBTK622-tdkkan-camR plasmid (ColE1 origin) doesn't replicate in ADP1, thus can be used as an additional negative control during transformations.

---++ Step 1: Golden Extension Reaction and Transformation for tdk/kan cassette insertion
<p style="font-size:150%">Primer design</p>
</br>
 The [[http://openwetware.org/wiki/User:Gabriel_A._Suarez/Notebook/ADP1_Baylyi_reference][tdk/kan cassette]] in the pBTK622 plasmid has *BsaI* sites at both ends of its sequence such that when cut by a BsaI enzyme &ndash; which cuts outside its recognition sequence - will leave the standard 4bp Golden Gate *type2/type4* sticky ends. In this procedure, a *BsaI* site is added to each flanking homology which is designed to provide the complementary *type2* and *type4* sticky ends, thereby allowing the correct assembly of the three parts as follows:

<b>Figure 2</b> Transformation cassette for the insertion of the tdk/kan cassette (red) generated by the Golden Extension reaction ligating homologous flanking regions (orange) to it. <br/>
<img width="802" alt="tdkkan_assembly.png" src="%ATTACHURLPATH%/tdkkan_assembly.png" height="103"/>

Each of the target&rsquo;s flanks needs to be amplified in independent PCR reactions, so only two sets of primers are required.

*Primer Set 1*: 5&rsquo;FW + GoldenRV5&rsquo; [5-ATGCGGTCTCACGTTCGTCTCAGACC (N)<sub>20</sub> -3&rsquo;] <br />N = ~20bp Reverse complement terminal sequence of 5'flanking homology

*Primer Set 2*: GoldenFW3&rsquo; [5-GCATGGTCTCAGCTGCGTCTCAGGTC (N)<sub>20</sub> -3&rsquo;] + 3&rsquo;Rv <br />N = ~20bp Fw terminal sequence of 3'flanking homology

Each set contains one *&ldquo;Golden Primer&rdquo;* (GoldenFW3&rsquo; or GoldenRV5&rsquo;) which contains ~20bp (denoted as a sequence of Ns) overlapping/targeting the flank to be amplified, plus BsaI and BsmBI sites. BsmBI sites will be used for construction of &ldquo;rescue&rdquo; cassette used to remove tdk/kan at the final stage of this protocol. See Figure 3 below for details. <br/> </br>
<b>Figure 3</b> Annealing of primers for amplification of homologous flanking regions by PCR. Restriction sites, which do not bind to template DNA, added to the end of each primer are shown in detail.
<img width="718.3'" alt="Figure_rescue.JPG" src="%ATTACHURLPATH%/Figure_rescue.JPG" height="226.05" />

The annealing temperatures for the &ldquo;Golden Primer&rdquo; are determined by the sequence of N&rsquo;s chosen (the overlapping sequence). It is critical that the primers on each set have about the same annealing temperature (aim 60C for Phusion pol). The Barrick Lab routinely uses the NEB Tm Calculator (http://tmcalculator.neb.com/#!/) to determine primer annealing temperatures and IDT&rsquo;s OligoAnalyzer Tool (https://www.idtdna.com/calc/analyzer) to check for hairpins or self-dimers, thus avoiding most common problems in primer design.

%X% Additional BsaI or BsmBI sites on the 3'-flank or 5'-flank chosen should not be a problem (so far has never been observed to be an issue), since these would generate unique sticky ends which would re-ligate during the Golden Extension Reaction. If you want to be extra careful, you can select flanks with fewer or none of these present in them. <br/>
%X% The genome binding segments of GoldenFW and GoldenRV primers should not overlap, even if the intention is to generate an insertion and not a deletion. Overlapping GoldenFw and GoldenRv primers leads to failed transformations.

<p style="font-size:150%">Reaction conditions</p>
</br>
 1. Use *set1* and *set2* primers to run PCR reactions to amplify both flanking regions of the target deletion/replacement site. <br/>2. Run a gel electrophoresis to verify that the correct PCR product size was amplified. <br />3. Purify the PCR products using PCR purification columns and measure the DNA concentrations. <br/>4. In a PCR tube, setup the BsaI Golden Extension Reaction with the following:

&emsp;- Reaction components - <br/>
&emsp;2 &mu;L of 10X T4 DNA ligase buffer (NEB: M0202S) <br/>
&emsp;1 &mu;L BsaI-HF (NEB: R3535S) <br/>
&emsp;1 &mu;L of T7 DNA ligase (NEB: M0318S)** <br/>
&emsp;250ng pBTK622-tdkkan-CamR plasmid <br/>
&emsp;150 ng 5&rsquo;flank homology (for ~1000bp)* <br/>
&emsp;150 ng 3&rsquo;flank homology (for ~1000bp)* <br/>
&emsp;dH2O to 20µL rxn total volume

*Depending on the length of each flank homology, fragment (flanks) to plasmid ratio can be adjusted to achieve the optimal 1:1:1 for each part, considering that the tdk/kan cassette is only 1.7kb and about half the size of the pBTK622-tdkkan-CamR plasmid (3.3kb). Click [[http://cels.uri.edu/gsc/cndna.html][here for a simple DNA molecule copy-number calculator]]. Also, the [[http://www.promega.com/a/apps/biomath/index.html?calc=ugpmols][Promega ug to pmol calculator]], the [[http://www.endmemo.com/bio/dnacopynum.php][DNA copy number calculator]] and the [[http://www.molbiol.edu.ru/eng/scripts/01_07.html][DNA mole conversion calculator]] are useful for balancing out quantities.

For more Golden Gate rxn details, see the [[Trash.ProtocolsGoldenGateAssembly][Golden Gate Assembly Protocol]] <br />**T4 ligase (NEB: M0202) may be used instead, but T7 ligase is preferred because it rarely generates any blunt ligation products and thus yields minimal off-target ligation. T7 ligase buffer is avoided because it contains PEG which is known to inhibit electroporation, although its effects on natural competence are unknown.

5. Run thermocycler with the following setting: <br/>
&emsp;1) 37°C, 5:00 <br/>
&emsp;2) 16°C, 5:00 <br/>
&emsp;3) Goto 1, 30X <br/>
&emsp;4) 55°C, 5:00 <br/>
&emsp;5) 80°C, 5:00 <br/>
&emsp;6) 12°C, &infin;

*Transformation steps:* <br />6. Prepare two tubes with 500 µL LB media + 35 µL overnight culture. Label one &ldquo;NoDNA control&rdquo; and the other &ldquo;DNA+&rdquo;. <br />7. Add all 20 µL of the Golden Gate rxn to the tube labeled &ldquo;DNA+&rdquo;. <br />8. Incubate overnight (or at least 6hrs) at 30C, 200 rpm. <br />9. Plate 100 µL of the transformation mix into an LB-Kan plate and incubate overnight. Plate also 100µL of the &ldquo;NoDNA&rdquo; negative control on another LB-Kan plate ([[https://advanced.bact.wisc.edu/instr/book/displayarticle/103][Click here for cell count and dilution basics]]). <br />10. Select 2-3 colonies to grow in liquid LB-Kan and proceed to confirm deletion/replacement in each by PCR.

Note: This procedure is yet to be tested using different size flanking homologies and varying amounts of DNA, two critical factors that affect transformation efficiencies. Under the specified conditions, the transformation efficiency observed is roughly 1.25 x 10<sup>&ndash;5</sup>, thus plating 100 µL will yield ~1000 colonies (ADP1-ISx strain) and why it's recomended to also plate 100x dilutions to make it easier to later pick out single colonies. It may be possible to obtain a good amount of transformants using lower DNA concentrations, which would be useful if you have lower quantities of any of the parts previous to the assembly or if you need to do multiple transformations with the 20 µL Golden Gate rxn product (e.g., use only 10 µL per transformation mix).

---++ Step 2: Tdk/kan cassette &ldquo;rescue&rdquo; (Genomic deletion or insertion and removal of tdk/kan marker with minimal 4bp scar)
<p style="font-size:150%">Deletion primer design</p>
</br>
For deletion of the targeted region the primers and flanking regions from Step 1, above, can be used. Digestion with BsmBI allows them to be ligated together without the tdk/kan cassette, creating a substrate for rescue of the cassette with the removal of the region between the flanks.

<p style="font-size:150%">Deletion reaction conditions</p>
</br>
1. Ligate 3&rsquo;-flank to 5&rsquo;-flank (using same PCR products step#3 above) by BsmBI Golden Gate assembly. <br/> <br/>
&emsp;- Reaction components - <br/>
&emsp;2 &mu;L of 10X T4 DNA ligase buffer (NEB: M0202S) <br/>
&emsp;1 &mu;L BsmBI (NEB: R0580S) <br/>
&emsp;1 &mu;L of T7 DNA ligase (NEB: M0318S) <br/>
&emsp;100 ng 5&rsquo;flank homology <br/>
&emsp;100 ng 3&rsquo;flank homology <br/>
&emsp;dH2O to 20µL rxn total volume

Tips and general Golden Gate Assembly protocol: http://barricklab.org/twiki/bin/view/Trash/ProtocolsGoldenGateAssembly)

Run thermocycler with the following setting (or as described before with shorter one-minute incubation times). <br/>
&emsp;1) 37°C, 5:00 <br/>
&emsp;2) 16°C, 5:00 <br/>
&emsp;3) Goto 1, 30X <br/>
&emsp;4) 55°C, 5:00 <br/>
&emsp;5) 80°C, 5:00 <br/>
&emsp;6) 12°C, &infin;

2. Repeat transformation steps above, but this time plate on LB-AZT (include a 100X dilution of the DNA+ and NoDNA control to make sure you can pick out single colony isolates, and because AZT in the NoDNA plate can be overcome by high numbers of cells.)*. Once colonies are visible, select 3-5 to grow in liquid LB and confirm tdk/kan removal by PCR using the 5'-flank FW primer with the 3'-flank RV primer (e.g., a positive result will produce an approximately 2kb band). Successful confirmation (strongly recommended) can be additionally supported by confirming their lack of growth on LB-kan (negative control), see [[ProtocolsAntibioticRemovalVerification][Quick 3hr Antibiotic Rescue Verification]].

*You may want to determine your rate of "rescue", equal to the transformation rate minus the mutation rate. For this, you will plate 100uL of 100x dilution of your 500uL overnight culture, grown without DNA, on LB and on LB-AZT. If successful, you will see many colonies on LB (transformation+mutation), and few or no colonies on LB-AZT (mutation). If you do not obtain these results, you will want to run through the following troubleshooting steps:<br />1. Verify that you are plating an adequate dilution of your overnight culture _e.g._ 100x. If you have a high concentration of cells _e.g._ &gt;10^10 and if your mutation rate is high, plating 100uL of overnight culture directly onto LB-AZT can result in a lawn.<br />2. Check that you are using the correct AZT working concentration (200ug/mL). That is, 400uL of AZT (stock = 10mg/mL) in 20mL of agar.<br />3. Regrow your overnight culture in LB-Kan to ensure the removal of possible contaminants.<br />4. Check the date of your AZT and remake your liquid stock if necessary. For 30mL of 10mg/mL AZT, add 0.3g of powder AZT to 30mL DIW. Filter sterilize solution by pushing it through a 50 mL syringe fitted with a 0.22 µm filter. Label and store at -20°C.

<p style="font-size:150%">Insertion primer design</p>
</br>
For insertion of a PCR product into the genome by rescuing an inserted tdk/kan cassette the desired PCR product should be amplified with primers creating BsaI overhangs complimentary to the primers from Step 1 using Primer Set 3, below. The insert DNA can then be joined to the homology flanks by digestion with BsaI and ligation (Figure X).

&emsp; *Primer Set 3* <br/>
&emsp; Forward [5-ATGCGGTCTCAAACG (N)<sub>20</sub> -3&rsquo;] <br />
&emsp; N = ~20bp Sequence of the beginning of the desired PCR product <br/>
&emsp; Reverse [5-GCATGGTCTCACAGC (N)<sub>20</sub> -3&rsquo;] <br />
&emsp; N = ~20bp Reverse complement of the end of the desired PCR product

<b>Figure 4</b> Transformation cassette for insertion of target DNA (green) by rescue of the tdk/kan cassette.</br>
<img width="801" alt="insert_assembly.png" src="%ATTACHURLPATH%/insert_assembly.png" height="103"/> </br>

When ligating multiple parts together, for example when combining flanking homology regions with a promoter and a coding region (Figure 5), each ligation site should use a different four base overhangs. While any set of four base overhangs should work the following have been estimated to ligate with the highest fidelity and thus make the best choices for complex, multipart ligation reactions: 5'-AGGA-3', 5'-AGAA-3', 5'-GAAA-3', 5'-GGAA-3', 5'-ATGA-3', 5'-AAGT-3', 5'-ATTC-3', 5'-CTGA-3', 5'-AAGA-3', 5'-CGGA-3', 5'-AAAT-3', 5'-GAGA-3', 5'-ACGA-3', 5'-CGAA-3', 5'-AAAA-3', 5'-GTAA-3', 5'-TCCA-3', 5'-AGAT-3', and 5'-AATA-3' (Pryor _et al_., 2020).

<b>Figure 5</b> Example transformation cassette for insertion of a multipart construct by rescue of the tdk/kan cassette. In this example a construct consisting of a new promoter (blue) attached to a coding region (green) will be inserted into the genome.</br>
<img width="978" alt="multipart_assembly_v2.png" src="%ATTACHURLPATH%/multipart_assembly_v2.png" height="98.5"/> </br>

<p style="font-size:150%">Insertion reaction conditions</p>
</br>
As "Deletion reaction conditions" above, except using this reaction mix: </br>

&emsp;- Reaction components - <br/>
&emsp;2 &mu;L of 10X T4 DNA ligase buffer (NEB: M0202S) <br/>
&emsp;1 &mu;L BsaI-HF (NEB: R3535S) <br/>
&emsp;1 &mu;L of T7 DNA ligase (NEB: M0318S) <br/>
&emsp;100 ng 5&rsquo;flank homology <br/>
&emsp;100 ng 3&rsquo;flank homology <br/>
&emsp;x ng insert DNA</br>
&emsp;dH2O to 20µL rxn total volume

The amount of insert DNA should be calculated relative to the homology flanks using one of the calculators in Step 1: Reaction Conditions, above.

---++ Tdk/kan cassette &ldquo;rescue&rdquo; with allele replacement (removal of tdk/kan to introduce mutations) 

If the aim is to introduce point mutations or you want to introduce genes, promoters or other genetic elements into ADP1's chromosome, first perform the tdk-kan replacement step and then generate the desired genetic sequence with >500bp flanking homologies (ordered as a gBlock, assembled via extension PCR or PCRed from a mutant variant) and use it to perform the "rescue" step described above. 

---++ References
* Pryor J.M., Potapov V., Kucera R.B., Bilotti K., Cantor E.J., and Lohman G.J.S. 2020. Enabling one-pot Golden Gate assemblies of unprecedented complexity using data-optimized assembly design. PLoS One 15(9),  e0238592.<br/>
* Suárez G.A., Dugan K.R., Renda B.A., Leonard S.P., Gangavarapu L.S., and Barrick J.E. 2020. Rapid and assured genetic engineering methods applied to _Acinetobacter baylyi_ ADP1 genome streamlining. Nucleic Acids Research 48(8), 4585–4600.
Barrick Lab > ProtocolList > ProtocolsAcinetobacterGoldenTransformation
Topic revision: r37 - 2021-05-17 - 18:32:11 - Main.IsaacGifford