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Cultivarium JERBOA Toolkit
(Kit # 1000000275 )

Depositing Lab:   Nili Ostrov, Charlie Gilbert, Cultivarium Tools

The JERBOA Toolkit (Jumping Element libRaries with Broad hOst rAnge) is a Golden Gate genetic toolkit developed to help researchers identify functional transposons and establish genetic tractability in diverse non-model bacteria. The kit enables high-throughput, pooled library screening of thousands of transposon configurations (varying transposases, antibiotic resistance markers, and promoter-RBS elements driving their expression) to determine the optimal construct for a specific host.

This kit will be sent as bacterial glycerol stocks in 96-well plate format.

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$440 USD + shipping
Available to academics and nonprofits only.

Original Publication

A scalable transposon mutagenesis system for non-model bacteria Gilbert C, Leung J, Crits-Christoph A, Kang SC, Esmurria A, Fenn K, Brumwell SL, Martin-Moldes Z, Mendler K, Barnum TP, Nguyen M-A, Lee HH, Ostrov N. bioRxiv 2025.12.22.696024. doi: 10.64898/2025.12.22.696024. Article (Link opens in a new window).

Description

Establishing genome-wide transposon mutagenesis in non-model microbes is often hindered by unpredictable host factors affecting transposase activity and selectable marker performance. The JERBOA Toolkit addresses this by providing a standardized, scalable framework for transposon variant screening.

The toolkit consists of the following modular parts that can be assembled to create transposon variant libraries:

  • Transposase systems: both hyperactive Himar1 (mariner) and Tn5 transposases.
  • Selectable markers: six commonly-used bacterial antibiotic resistance (ABR) genes (KAN, GEN, ERM, TET, CAM, and SPEC).
  • Promoter variants: 18 diverse promoter-5' UTR sequences (including 16 broad-host-range promoters, a "dummy" negative control promoter, and standard resistance marker gene/transposase gene promoters) to independently drive the transposase and ABR marker.
  • Combinatorial scale: the system supports up to 3,888 unique configurations (2 transposases × 6 markers × 18 transposase promoters × 18 ABR promoters).

Each unique final transposon variant plasmid possesses a unique DNA barcode within the transposon, allowing for quantification of transposition efficiency via Tn-seq or Semi-arbitrary (SemiArb) PCR. This approach has been validated across 92 non-model bacteria, identifying functional tools for species with no previously described genetic systems.

Schematics of kit plasmids and overview. The 36 transposase promoter variant plasmids contain ColE1, kan; and transposase promoter ID barcode, primer binding, and transposase promoter variants between in-built BsaI restriction enzyme cut sites and overhangs. The 23 ABR promoter variant plasmids contain ColE1, kan; and ABR promoter variant, primer binding, and ABR promoter ID barcode between in-built BsaI restriction enzyme cut sites and overhangs. The 12 transposon plasmid destination vectors contain mSc; and Himar1/Tn5, ori, R6K, carb, Himar1/Tn5 RE, and ABR between in-built BsaI restriction enzyme cut sites and overhangs. BsaI Golden Gate assembly allows the construction of single plasmids made up of a part between the cut sites from each of the three plasmid categories. The collection of different single plasmids form transposon variant libraries.

Figure 1: Overview of the JERBOA Toolkit. The toolkit is designed for the modular construction and high-throughput screening of barcoded transposon libraries. The toolkit provides three categories of plasmids: 36 transposase promoter part plasmids, each carrying a bacterial promoter sequence paired with either a Himar1 or Tn5 left mosaic end (LE) and a unique promoter ID barcode; 23 ABR gene promoter part plasmids, each carrying a bacterial promoter sequence and unique ID barcode; and 12 transposon destination vectors featuring either a Himar1 or Tn5 transposase and one of six ABR genes. In-built BsaI restriction enzyme cut sites and overhangs (red triangle and red circle) enable Bsal Golden Gate assembly, and assembly of pooled libraries of up to 3,888 unique transposon variants. Each final construct contains unique barcodes within the transposon for identification via Tn-Seq as well as an RK2/RP4 origin of transfer (oriT) for conjugative delivery, a conditional R6Kγ origin, and a carbenicillin (carb) marker for selection in the E. coli donor.

Kit Documentation

Cultivarium JERBOA Toolkit plasmid sequences (ZIP, 171 KB)

How to Cite this Kit

These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which they were created, and include Addgene in the Materials and Methods of your future publications.

For your Materials and Methods section:

"The Cultivarium JERBOA Toolkit was a gift from Nili Ostrov, Charlie Gilbert, and Cultivarium Tools (Addgene kit #1000000275)."

For your Reference section:

A scalable transposon mutagenesis system for non-model bacteria Gilbert C, Leung J, Crits-Christoph A, Kang SC, Esmurria A, Fenn K, Brumwell SL, Martin-Moldes Z, Mendler K, Barnum TP, Nguyen M-A, Lee HH, Ostrov N. bioRxiv 2025.12.22.696024. doi: 10.64898/2025.12.22.696024. Article (Link opens in a new window)

Cultivarium JERBOA Toolkit - #1000000275

Resistance Color Key

Each circle corresponds to a specific antibiotic resistance in the kit plate map wells.

Inventory

Searchable and sortable table of all plasmids in kit. The Well column lists the plasmid well location in its plate. The Plasmid column links to a plasmid's individual web page.

Kit Plate Map

96-well plate map for plasmid layout. Hovering over a well reveals the plasmid name, while clicking on a well opens the plasmid page.

Resistance Color Key

Chloramphenicol
Ampicillin
Kanamycin

Inventory

Well Plasmid Resistance
A / 1 pGLU_63
Chloramphenicol
A / 2 pGLU_64
Chloramphenicol
A / 3 pGLU_66
Chloramphenicol
A / 4 pGLU_67
Chloramphenicol
A / 5 pGLU_68
Chloramphenicol
A / 6 pGLU_69
Chloramphenicol
A / 7 pGLU_71
Chloramphenicol
A / 8 pGLU_72
Chloramphenicol
A / 9 pGLU_73
Chloramphenicol
A / 10 pGLU_74
Chloramphenicol
A / 11 pGLU_75
Chloramphenicol
A / 12 pGLU_76
Chloramphenicol
B / 1 pGLU_77
Chloramphenicol
B / 2 pGLU_79
Chloramphenicol
B / 3 pGLU_80
Chloramphenicol
B / 4 pGLU_81
Chloramphenicol
B / 5 pGLU_82
Chloramphenicol
B / 6 pGLU_103
Chloramphenicol
B / 7 pGLU_104
Chloramphenicol
B / 8 pGLU_105
Chloramphenicol
B / 9 pGLU_107
Chloramphenicol
B / 10 pGLU_108
Chloramphenicol
B / 11 pGLU_109
Chloramphenicol
B / 12 pGLU_110
Chloramphenicol
C / 1 pGLU_111
Chloramphenicol
C / 2 pGLU_112
Chloramphenicol
C / 3 pGLU_113
Chloramphenicol
C / 4 pGLU_115
Chloramphenicol
C / 5 pGLU_116
Chloramphenicol
C / 6 pGLU_117
Chloramphenicol
C / 7 pGLU_118
Chloramphenicol
C / 8 pGLU_119
Chloramphenicol
C / 9 pGLU_85
Chloramphenicol
C / 10 pGLU_86
Chloramphenicol
C / 11 pGLU_87
Chloramphenicol
C / 12 pGLU_89
Chloramphenicol
D / 1 pGLU_90
Chloramphenicol
D / 2 pGLU_91
Chloramphenicol
D / 3 pGLU_92
Chloramphenicol
D / 4 pGLU_93
Chloramphenicol
D / 5 pGLU_94
Chloramphenicol
D / 6 pGLU_95
Chloramphenicol
D / 7 pGLU_97
Chloramphenicol
D / 8 pGLU_98
Chloramphenicol
D / 9 pGLU_99
Chloramphenicol
D / 10 pGLU_100
Chloramphenicol
D / 11 pGLU_101
Chloramphenicol
D / 12 pGLU_7
Ampicillin
E / 1 pGLU_8
Ampicillin
E / 2 pGLU_9
Ampicillin
E / 3 pGLU_10
Ampicillin
E / 4 pGLU_11
Ampicillin
E / 5 pGLU_12
Ampicillin
E / 6 pGLU_128
Ampicillin
E / 7 pGLU_129
Ampicillin
E / 8 pGLU_130
Ampicillin
E / 9 pGLU_131
Ampicillin
E / 10 pGLU_132
Ampicillin
E / 11 pGLU_133
Ampicillin
E / 12 pGLU_62
Kanamycin
F / 1 pGLU_65
Kanamycin
F / 2 pGLU_83
Kanamycin
F / 3 pGLU_120
Kanamycin
F / 4 pGLU_70
Chloramphenicol
F / 5 pGLU_78
Chloramphenicol
F / 6 pGLU_84
Chloramphenicol
F / 7 pGLU_106
Chloramphenicol
F / 8 pGLU_114
Chloramphenicol
F / 9 pGLU_88
Chloramphenicol
F / 10 pGLU_96
Chloramphenicol
F / 11 pGLU_102
Chloramphenicol
Data calculated @ 2026-03-12

Kit Plate Map - #1000000275

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