| Strain Descriptor |
Strain Summary |
Genotype |
Phenotype |
| HU2305 | | mut, hu2305 | |
| HU2421 | Tester strain | pspA352 (28 kd), pspB352, bsgA5, modB501, modB | bsg |
| HU2460 | Tester strain | pspA353, pspB353, modB501, tsgK1, sup379, couA351 | |
| HU2470 | tester strain, mutant of the epitope of the MUD62 mAb | mut, hu2470 | |
| HU2471 | tester strain, mutant of the epitope of the MUD62 mAb; mutation also affects the size of pspA | mut, pspA, hu2471 | |
| HU26/NP167/X55 | tester strain; Parents: HU26, NP167 (DBS0236637), X55(DBS0237084) | sprA/+, tsgE/+, whiA/+, acrA/acrA, tsgD12/+, axeA1/+, axeB1/+, tsgB1/+, ebr404/+, cobD | |
| HU2708 | tester strain | hu2708 | |
| HU2733 | tester strain | hu2733 | |
| HU407 | tester strain (Rob Kay''''''''s lab) | bsgA5, bwnA1, couA351, cycA1 or 5, frtB353, manA2, tsgK21 | brown,cycR,bsg,couS,tsg,frt |
| HU409 | Slug phototaxis mutant. | whi, tsgD12, tsgE13, acrA1, sprA1 | metR, tsg, whi |
| HU440 | tester strain | hu440 | |
| HU60 | tester strain | axeA1, axeB1, axeC1.cycA1, oaaA1, supA1, tsgA1, bwnA1 | axe,tsg,cycR |
| HU835 | tester strain | hu835 | |
| HU845 | tester strain | hu845 | |
| HUD1 | The haploid segregant has WS380B linkage groups I, II, IV, V, and VII. It has the HU1852 linkage group III with the whiB355 marker and the HU1852 linkage group VI with the manA2 marker. It was cobB354, which is the unstable cobalt resistance. | whiB355, manA2, cobB354 | whi |
| HUD28 | | mut, hud28 | |
| HUD33 | | mut, hud33 | |
| HUD34 | | mut, hud34 | |
| HUD6 | | mut, hud6 | |
| HUD7 | Tester strain | mut, hud7 | |
| HV32 | tester strain; lousy tsg; some confusion about the phg locus here, could also be phgA1356 | matA1, axeA1, axeC1, axeB1, phgA1356, tsg-1356 | |
| I-8 | uracil auxotroph | axeA2.axeB2, axeC2, pyr5-6-[pISAR], ura-, neoR | axe,ura-,neoR |
| I6KA- | inositol hexakisphosphatephosphate kinase null | axeA2, axeB2, axeC2, I6KA-[KO-vector], bsR | axe,wt,bsR |
| I6KA- | I6KA null mutant in AX2 | axeA2, axeB2, axeC2, I6KA-, [TMO1], bsR | |
| ibrA- | ibrA null mutant with the BsR cassette removed | axeA1, axeB1, axeC1, ibrA- | |
| ibrA- | ibrA null strain in AX2 | axeA2, axeB2, axeC2, ibrA-, [bsRcas], bsR | |
| icmA- | icmA null mutant; both copies of the gene in AX4 were deleted. | axeA1, axeB1, axeC1, icmA-, bsR | |
| icmA-/[act15]:hICMT | icmA null mutant rescued by expression of the human ICMT | axeA1, axeB1, axeC1, icmA-, ICMT, bsR, neoR | |
| icmA-/[act15]:icmA | icmA null mutant rescued by expression of icmA | axeA1, axeB1, axeC1, icmA-, icmA, bsR, neoR | |
| icmA-/[act15]:TAP:YFP:rasG | TAP-YFP-RasG fusion expressed in a icmA null mutant | axeA1, axeB1, axeC1, icmA-, YFP-rasG, bsR, neoR | |
| icpA- | icpA-null mutant. Two independent cell lines are available: 10B6 and 10H10. | axeA2, axeB2, axeC2, icpA-, bsR | axe, bsR |
| icpA-/[act15]:GFP:icpA | GFP-icpA expressed in icpA-null cells. The complemented null strain shows the same localization as the transformed wild-type strain (personal communication, ADL, 8/30/07) | axeA2, axeB2, axeC2, icpA-, bsR, [GFP-icpA], neoR | axe, bsR, neoR |
| icpA-/[act15]:GFP:icpA(1-1013) | INCENP-null cells transformed with GFP-DdINCENP1-1013 | axeA2, axeB2, axeC2, icpA-, bsR, pTX-INCENP-ΔC, neoR | axe, bsR, neoR |
| icpA-/[act15]:GFP:icpA(1-500) | INCENP-null cells transformed with GFP-DdINCENP1-500 | axeA2, axeB2, axeC2, icpA-, bsR, pTX-INCENP-ΔCs1, neoR | axe, bsR, neoR |
| icpA-/[act15]:GFP:icpA(488-1320) | icpA null mutant transformed with GFP-DdINCENP488-1320 | axeA2, axeB2, axeC2, icpA-, bsR, pTX-INCENP-ΔN, neoR | axe, bsR, neoR |
| icpA-/[unk]:GFP:mhcA | icpA null mutant expressing GFP-mhcA | axeA2, axeB2, axeC2, icpA-, [GFP-mhcA] | |
| icpA-/[unk]:mtaA:GFP | icpA null mutant expressing mtaA-GFP | axeA2, axeB2, axeC2, icpA-, [mtaA-GFPOE] | |
| ifkA- | ifkA null mutant in AX4 | axeA1, axeB1, axeC1, ifkA-, bsR | |
| ifkA-/ifkB- | ifkA/ifkB double null mutant | axeA1, axeB1, axeC1, ifkA-, ifkB-, bsR, hygR | |
| ifkB- | ifkB null | axeA1, axeB1, axeC1, ifkB-, bsR | |
| ino1- | ino1 null mutant; inositol auxotroph | axeA2, axeB2, axeC2, ino1-, bsR | |
| ino1- | ino1 null in AX2 | axeA2, axeB2, axeC2, ino1-, [bsRcas], bsR | |
| iplA- | iplA null mutant in DH1-10 background | axeA1, axeB1, axeC1, pyr5-6- [pRG24], ura-, iplA-, [bsRcas], bsR | |
| iplA- | iplA- null mutant in HMX44A (cell line that is able to develop as a monolayer) | axe, tsg-901 and/or tsg-903, cyc-900, dif, plA-[iplA(ins)], bsR | |
| iplA- | iplA null mutant; iplA encodes the IP3 receptor which is required to signal autophagic cell death. | axeA1, axeB1, axeC1, pyr5-6-[pRG24], ura-, iplA-[iplA(ins)], bsR | axe, ura-, bsR |
| iplA- | iplA null mutant | axeA2, axeB2, axeC2, iplA-[pDT5], bsR | axe, small fruiting bodies, bsR |
| iplA-/AX2 | iplA null mutant in AX2 | axeA2, axeB2, axeC2, iplA-, [bsR-loxP], bsR | |
| iplA-/[act15]:GFP:iplA | N-terminal GFP-tagged IplA expressed in iplA null mutant | axeA2, axeB2, axeC2, iplA-, [pDT5], GFP:iplA, bsR, neoR | |
| iptA- | iptA null mutant | axeA1, axeB1, axeC1, bsR, iptA- | |
| iqgC- | iqgC null mutant | axeA1, axeB1, axeC1, iqgC-, [bsRcas], bsR | |
| iqgC- | iqgC null mutant in AX2 | axeA2, axeB2, axeC2, iqgC-, [bsR-loxP], bsR | |
| IR1 | Mating-type tester strain A2cycR, made axenic by about 3 months selection in rich medium on plates (pers. communication). | axe, cyrR, matA2 | |
| IR110 | AX3 cells with thyA disrupted by neoR. | axeA1, axeB1, axeC1, thyA-[pGEM25+pA15-neoR], thy-, neoR | axe,neoR,thy- |
| IR120 | AX3 cells with thyA disrupted by hygR | axeA1, axeB1, axeC1, thyA-[pGEM25+pA15-hygR], thy-, hygR | axe,hygR,thy- |
| IR3 | Mating-type tester strain, made by crossing IR1 with WS205, hatching the macrocysts, cloning, and selecting the ones that grew axenically and were the opposite mating type to IR1 (pers. communication). | axe, cyc, matA1 | cycR,axe,wt |
| ireA- | ireA null mutant in AX4 | axeA1, axeB1, axeC1, ireA, [pGEM-T-Easy], bsR | |
| ireA-/[act15]:ireA(K603N):GFP | GFP-marked ireA with K603N substitution rendering kinase inactive, overexpressed in ireA null | axeA1, axeB1, axeC1, ireA, [pGEM-T-Easy], ireA(K603N), [pDM323], bsR, neoR | |
| ireA-/[act15]:ireA(N927A):GFP | GFP-marked ireA with N927A substitution rendering RNAase inactive, overexpressed in ireA null | axeA1, axeB1, axeC1, ireA, [pGEM-T-Easy], ireA(N927A), [pDM323], bsR, neoR | |
| JC2 | slugger | slgC701 | slugger |
| JC4 | slugger | slgC702 | slugger |
| JH.D | cbfA(amber) mutant | axeA2, axeB2, axeC2, cbfA(amber)[pJH1.2(am)-tetO:Glu(su)], bsR | axe,nearly agg-,bsR |
| JH.D(ura-) | cbfA(amber) mutant | axeA2, axeB2, axeC2, cbfA(amber)[pJH1.2(am)-tetO:Glu(su)], bsR, ura- | axe,ura-,nearly agg-,bsR |
| JH10 | thymidine auxotroph (original Jeff Hadwiger strain) | axeA1, axeB1, axeC1, pyr5-6-[PYR5-6-SalI-linker], thy-[PYR5-6-THY1], ura+, thy- | axe,thy-,ura+ |
| JH10 | thymidine auxotroph (Rob Insall lab strain) | axeA1, axeB1, axeC1, pyr5-6-[PYR5-6-SalI-linker], thy-[PYR5-6-THY1], ura+, thy- | axe,thy-,ura+ |
| JH10 | thymidine auxotroph (Rex Chisholm) | axeA1, axeB1, axeC1, pyr5-6-[PYR5-6-SalI-linker], thy-[PYR5-6-THY1], ura+, thy- | axe, thy-, ura+ |
| JH10 | thymidine auxotroph (Graham Cote lab) | axeA1, axeB1, axeC1, pyr5-6-[PYR5-6-SalI-linker], thy-[PYR5-6-THY1], ura+, thy- | axe,thy-,wt |
| JH10 | Thymidine auxotroph (Gerry Weeks lab strain) | axeA1, axeB1, axeC1, pyr5-6-[PYR5-6-SalI-linker], thy-[PYR5-6-THY1], ura+, thy- | axe, thy-, ura+ |
| JH10 | Thymidine auxotroph (Rick Firtel lab strain) | axeA1, axeB1, axeC1, pyr5-6-[PYR5-6-SalI-linker], thy-[PYR5-6-THY1], ura+, thy- | axe,thy-,ura+ |
| JH10 | generic thymidine auxotroph strain, used for curation of parental strains when the specific JH10 is not available | axeA1, axeB1, axeC1, pyr5-6-[PYR5-6-SalI-linker], thy-[PYR5-6-THY1], ura+, thy- | |
| JH8 | uracil auxotroph | axeA1, axeB1, axeC1, py5-6-[PYR5-6-SalI-linker], ura- | axe,ura- |
| K. aerogenes | bacterial strain Klebsiella aerogenes, formerly Aerobacter aerogenes, now Klebsiella pneumoniae; biosafety level 2 (USA); Cosson laboratory strain | k.aerogenes | |
| K. aerogenes | bacterial strain Klebsiella aerogenes, formerly known as Aerobacter aerogenes, now also known as Klebsiella pneumoniae; biosafety level 2 (USA) | k.aerogenes | |
| K. aerogenes cobR | bacterial strain Klebsiella aerogenes, cobR; biosafety level 2 (USA) | k.aerogenes, cobR | |
| K. aerogenes GFP | bacterial strain Klebsiella aerogenes, formerly Aerobacter aerogenes, now Klebsiella pneumoniae; biosafety level 2 (USA); this Ka strain expressing GFP was obtained by introducing the GFP-expressing plasmid pANT5 (Lee and Falkow, 1998) into the Cosson laboratory strain, ampR | k.aerogenes, ampR, GFP | |
| K. aerogenes hygR | bacterial strain Klebsiella aerogenes, hygR; biosafety level 2 (USA) | k.aerogenes, hygR | |
| K. aerogenes neoR | bacterial strain Klebsiella aerogenes, neoR; biosafety level 2 (USA) | k.aerogenes, neoR | |
| K. aerogenes WaaQ- kanaR | bacterial strain Klebsiella aerogenes, formerly Aerobacter aerogenes, now Klebsiella pneumoniae; biosafety level 2 (USA); this strain is mutated in WaaQ (a gene responsible for biosynthesis of the bacterial cell surface); kanamycin resistant; good food source for the phg1- and kil1- mutants; kanamycin resistant. | k.aerogenes, waaQ-, kanR | |
| K. planticola | bacterial strain Klebsiella planticola; biosafety level 1 (USA) | k.planticola | |
| K. pneumoniae | bacterial strain Klebsiella pneumoniae, formerly Klebsiella aerogenes and Aerobacter aerogenes; strain is avirulent (P1 security level Europe); genome has been completely sequenced (Lima et al., 2018); Cosson laboratory strain | k.aerogenes, KpGe | |
| KAX3 | Rick Firtel lab strain; axenic; clone of AX3 sent to Firtel by Kessin; reported to have higher transformation efficiency than AX3 | axeA1, axeB1, axeC1 | axe,wt |
| KAX3 | Hideko Urushihara lab strain; axenic; clone of AX3 sent to Firtel by Kessin; reported to have higher transformation efficiency than AX3 | axeA1, axeB1, axeC1 | axe,wt |
| KAX3 | Beth Luna lab strain; axenic; clone of AX3 sent to Firtel by Kessin; reported to have higher transformation efficiency than AX3 | axeA1, axeB1, axeC1 | axe,wt |
| KAX3 | generic axenic strain, used for curation of parental strains when the specific KAX3 is not available | axeA1, axeB1, axeC1 | |
| KAX3 | Axenic strain from the Rutherford Lab. | axeA1, axeB1, axeC1 | wt, axe |
| KAX3 | Jeff Hadwiger lab strain; axenic; clone of AX3 sent to Firtel by Kessin; reported to have higher transformation efficiency than AX3 | axeA1, axeB1, axeC1 | axe |
| KAX3 | Pierre Golstein lab strain; axenic; clone of AX3 sent to Golstein by Kessin | axeA1, axeB1, axeC1 | axe |
| kctd9- | kctd9 null mutant; blasticidin resistant | axeA1, axeB1, axeC1, kctd9-, bsR | |
| keaA- | keaA underexpressor expressed in AX4 cells; isolated as yakA suppressor | axeA1, axeB1, axeC1, keaA-, bsR | |
| KEAC | does not aggregate (agg-) | axeA1, axeB1 axeC1, keac, neoR | |
| KI-10 | agg-minus; lacks cGMP response | cycA5, bsgA5, agg- | agg-,cycR,bsg |
| kif1- | kif1 null mutant | axeA2, axeB2, axeC2, kif1-, [pUCBsrΔBam], bsR | |
| kif10- | kif10 null mutant expressed in AX2 cells | axeA2, axeB2, axeC2, kif10-, [bsR-loxP], bsR | |
| kif10-/[act15]:dhcA(1384-4725) | the motor domain of dynein heavy chain (dhcA) expressed in kif10 null mutant
| axeA2, axeB2, axeC2, kif10-, [act15]:dhcA(1384-4725), bsr, neoR | |
| kif11- | kif11 null mutant expressed in AX2 cells | axeA2, axeB2, axeC2, kif11-, [bsR-loxP], bsR | |
| kif12- | kif12 null mutant | axeA2, axeB2, axeC2, kif12-, bsR | axe, bsR |
| kif12-/[act15]:FLAG:kif12 | kif12 null mutant expressing kif12 under the control of the constitutive act15 promoter | axeA2, axeB2, axeC2, kif12-, bsR, [act15]:FLAG:kif12, neoR | |
| kif13- | kif13 null mutant | axeA2, axeB2, axeC2, kif13-, bsR | |
| kif1A- | this cell line is 5 bp deletion near the KIF1A N-terminal; clone 2 | axeA2, axeB2, axeC2, kif1A-, [pKIF1A-PTM1285] | |
| kif1A- | this cell line is 5 bp deletion near the KIF1A N-terminal; clone 1 | axeA2, axeB2, axeC2, kif1A-, [pKIF1A-PTM1285] | |
| kif2- | kif2 null in AX2 | axeA2, axeB2, axeC2, kif2-, [pUCBΔBam], bsR | |
