(r2) Barrick Lab :: ProtocolsAcinetobacterBaylyiADP1

---+ _Acinetobacter baylyi_ ADP1 Overview

---++ ADP1 Resources

   *  Genome Sequences
      * [[https://www.ncbi.nlm.nih.gov/nuccore/NC_005966.1][ADP1 Wild-Type (GenBank: NC_005966.1)]] %BR% In general, use this genome as a reference when referring to coordinates of genes and features in the ADP1 genome.
         * [[http://blast.ncbi.nlm.nih.gov/Blast.cgi?PAGE_TYPE=BlastSearch&USER_FORMAT_DEFAULTS=on&PAGE=MegaBlast&PROGRAM=blastn&GAPCOSTS=0%200&MATCH_SCORES=1,-2&BLAST_SPEC=MicrobialGenomes_62977&EQ_MENU=Acinetobacter%20sp.%20ADP1%20%28taxid%3A62977%29&DATABASE=Complete_Genomes&BLAST_PROGRAMS=megaBlast&MAX_NUM_SEQ=100&SHORT_QUERY_ADJUST=on&EXPECT=10&WORD_SIZE=28&TEMPLATE_TYPE=0&TEMPLATE_LENGTH=0&FILTER=L&FILTER=m&DB_GROUP=AllMG&SUBGROUP_NAME=All_genomes&DB_SUBGROUP=Complete_Genomes&SHOW_OVERVIEW=on&SHOW_LINKOUT=on&ALIGNMENT_VIEW=Pairwise&MASK_CHAR=2&MASK_COLOR=1&GET_SEQUENCE=on&NUM_OVERVIEW=100&DESCRIPTIONS=100&ALIGNMENTS=100&FORMAT_OBJECT=Alignment&FORMAT_TYPE=HTML&OLD_BLAST=false][BLAST a sequence against the ADP1 (WT) genome (at NCBI)]]
      * [[https://github.com/barricklab/Abaylyi-EE/raw/master/reference/Acinetobacter-baylyi-ADP1-WT.gff3][ADP1 Barrick (GenBank: NC_005966.1)]] %BR% Incorporates a small number of mutations found in the WT ADP1 strain that the Barrick lab originally obtained from Valérie de Crécy-Lagard. Use for analyzing NGS sequencing results.
      * [[][ADP1-ISx]] %BR% Strain created in the Barrick lab with all IS<i>1236</i> elements deleted. (NEEDS LINK)

   * Other Useful Sequences
      * [[https://github.com/barricklab/Abaylyi-EE/raw/master/reference/pBTK622_tdk-kanR_cassette_for%20Golden_Transformation.gbk][<i>tdk</i>-kanR cassette used for genome editing]]
 
   * Functional Genomics
      * [[https://www.genome.jp/kegg-bin/show_organism?org=T00185][ADP1 pathways and gene functions (KEGG)]] 
      * [[http://biocyc.org/organism-summary?object=ASP62977][ADP1 pathways and gene functions in (BioCyc)]] 

---++ Antibiotic Resistance

*ADP1 is intrinsically resistant to beta-lactam antibiotics.* Do not use plasmids/constructs that have beta-lactamase (_bla_) as the selectable marker gene for ampicillin (or carbenicillin) resistance. Most other common antibiotic selection markers can be used. 

We most commonly use kanamycin and spectinomycin resistance markers. The rate of spontaneous mutations to KanR is undetectable. SpecR mutants can arise at a low frequency (~10<sup>&minus;8</sup> to 10<sup>&minus;9</sup>) due to chromosomal mutations, so only use this marker for transformations that have a significantly higher frequency than this.

| *Antibiotic* | *MIC* | *Standard Conc.* | *Status* | *Notes* |
| Ampicillin (or carbenicillin) | 128 µg/ml | 100 µg/ml | %RED%Resistant%ENDCOLOR% | |
| Kanamycin | 12.5-6.25 µg/ml (3.125µg/mL doesn't inhibit) | 50 µg/ml | Sensitive | MIC info from Barrick Lab results (G.S.) |
| Spectinomycin | ? | 60 µg/ml | Sensitive | Spontaneous resistance |
| Streptomycin | 6.25-12.5 µg/ml (escapes observed at 6.25µg/mL) | 25 µg/ml | Sensitive | Barrick Lab results (G.S.) |
| Chloramphenicol | 4.0 µg/ml | 20 µg/ml | Sensitive | Spontaneous resistance  |
| Gentamycin | 1.3 µg/ml | 5 µg/ml | Sensitive | |
| Tetracycline | 1.0 µg/ml | 10 µg/ml | Sensitive | |
| Rifampicin | 0.6 µg/ml | 100 µg/ml | Sensitive | Spontaneous resistance |
| Nalidixic acid (mutagen/causes DNA double strand breaks) | 1.9 µg/ml (no growth at 24 hr, but growth at 48 hr) (1 µg/ml doesn't inhibit) | 3.75 µg/ml | Sensitive | Barrick Lab results (G.S.) |

*Source:* Gomez MJ, Neyfakh AA. (2006) Genes involved in intrinsic antibiotic resistance of _Acinetobacter baylyi_. _Antimicrob Agents Chemother_ *50*:3562&ndash;3567. [[https://doi.org/10.1128/AAC.00579-06][DOI: 10.1128/AAC.00579-06]]

---++ Plasmids

*Common high-copy number _E. coli_ plasmids do not work in ADP1.* A synthetic plasmid (pBAV1K) and broad-host-range plasmid (RSF1010) have been used successfully. In our hands, pBAV1K is less reliable. It is also important to note that because plasmid DNA is linearizes when taken up through the competence apparatus, that transformation of plasmids can be significantly less efficient than transformations used to incorporate DNA directly in the chromosome.

| *Origin* | *Copy Number* | *Example* |
| ColE1 (pUC, pBR322, etc.) type plasmids | %RED% Do not replicate %ENDCOLOR% | NA |
| pBAV1K | Low-medium copy number | [[https://www.addgene.org/26702/][pBAV1K-T5-gfp]] |
| RSF1010 | Low-medium copy number | [[https://www.addgene.org/110599/][pBTK403]] |
Barrick Lab > ProtocolList > ProtocolsAcinetobacterBaylyiADP1
Contributors to this topic
JeffreyBarrick, IsaacGifford
Topic revision: r2 - 2022-03-18 - 12:05:01 - Main.JeffreyBarrick