Definitions & Genotypes of Selected E. coli Strains

Genotypes, Phenotypes & Markers

For more in-depth information about blue-white screening, transformation, transfection, and related molecular cloning topics, explore our Molecular Biology Guide.

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Definitions

What is a Genotype?

A genotype is a list of mutant genes in an organism. In addition to mutations of the genome, other genetic elements such as prophage or plasmids can also be included. They are listed in brackets. The most popular prophages are DE3 (a λ derivative with the T7 RNA polymerase cloned in) and φ80dlacΔM15, which carries the half of the beta-galactosidase required for blue/white screening in plasmids like pUC19. The F plasmid also usually has a genotype because most F plasmids have E. coli chromosomal DNA in them. These are referred to as F’ (F prime).

It is assumed that any of the genes that are not mentioned in the genotype are wild type. A strain may have an unknown mutation. For example, JM109 is a lon mutant. The genotype of JM109 usually does not mention lon because it is not well known that it is there. It was discovered during the study of a different gene.1 Conversely, a mutation in a genotype does not always mean that the mutation is really there. At times, it has been deduced that the mutation is there based on the genotype from the properties of the parental strain. For example, almost every genotype claims that the HB101 is a proline auxotroph,2 but it has since been determined that it is not.3

What is a Phenotype?

A phenotype is a property that is genetically determined, but the mutated gene is unknown. For example, a strain that is resistant to phage T1 is referred to as T1R. The resistance could be due to an insertion sequence in the T1 receptor that is coded by the tonA gene (also known as the fhuA gene). If it is, the strain is referred to as tonA (or fhuA). If the tonA gene is found to be wild type, then another mutation must be causing the T1 resistance. Therefore, since it is still unknown, T1R is used to describe the strain. Another instance in which the phenotype is included is when the genotype does not clearly represent the trait. For example, the genotype rpsL indicates that the strain is resistant to streptomycin. StrR is used to indicate resistance to streptomycin instead as it clearly indicates the trait.

What is a Marker?

A marker is any mutation that distinguishes (“marks”) a strain. A marker can be a gene mutation or a phenotype. The presence of a prophage or of plasmids is not usually referred to as a “marker.”

Most likely, the strain that you are working with contains the mutations that you desire: recA, endA, lacΔM15, rpsL and tonA. However, it is important to remember that E. coli laboratory strains have been mutagenized, mixed up and transduced for years.4 As a result, the probability that the strain has all of the mutations in the genotype and only those mutations varies greatly. This is why trying different strain backgrounds is recommended when experiments are not working as expected.

Guide to E. coli Markers

References

  1. Robert Bebee, PhD. Thesis, 1998. George Washington University.
  2. Boyer, H.W. and Roulland-Dussoix, D. (1969) J. Mol. Biol. 41, 459.
  3. I. Serebrijski, O. Reyes, and G. Leblon. (1995) Corrected Gene Assignments of Escherishia coli Pro- Mutations. J. Bacteriol. 177(24):7261-7264.
  4. Berlyn, M.K.B. (1996) in F. C. Niedhardt et al. (Ed.), Escherichia coli and Salmonella: Cellular and Molecular Biology, (2nd ed.), Vol. 2, (pp. 1715-1902). ASM Press.

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Genotypes of Selected E. coli Strains

BL21 E. coli B F ompT gal [E. coli B is naturally dcm and lon] hsdSB

BL21(DE3) E. coli B F ompT gal [E. coli B is naturally dcm and lon] hsdSB with DE3, a λ prophage carrying the T7 RNA polymerase gene and lacIQ

C600 F [e14– (McrF) or e14+ (McrF+)] thr-1 leuB6 thi-1 lacY1 glnV44 rfbD1 fhuA21

CJ236 F Δ(HindIII)::cat (Tra+ Pil+ CamR )/ ung-1 relA1 dut-1 thi-1 spoT1 mcrA

GC5 F´ endA1 hsdR17 (rKmK+) glnV44 thi-1 recA1 gyrA (Nalr) relA1 Δ(lacIZYA-argF)U169 (φ80dlacΔ(lacZ)M15 fhuA

GM48 F thr leu thi lacY galK galT ara fhuA tsx dam dcm glnV44

HB101 F Δ(gpt-proA)62 leuB6 glnV44 ara-14 galK2 lacY1 Δ(mcrC-mrr) rpsL20 (Strr) xyl-5 mtl-1 recA13

JM83 F ara Δ(lac-proAB) rpsL (Strr)[φ80 dlacΔ(lacZ)M15] thi

JM101 F´traD36 proA+B+ lacIq Δ(lacZ)M15/ Δ(lac-proAB) glnV thi

JM103 F´ traD36 lacIqΔ(lacZ)M15 proA+B+/endA1 glnV sbcBC thi-1 rpsL (Strr) Δ(lac-pro) (P1) (rK–mK+ rP1+ mP1+)

JM105 F´ traD36 lacIqΔ(lacZ)M15 proA+B+/thi rpsL (Strr) endA sbcB15 sbcC hsdR4 (rK–mK+) Δ(lac-proAB)

JM107 F´ traD36 lacIq Δ(lacZ)M15 proA+B+/e14(McrA) Δ(lac-proAB) thi gyrA96 (Nalr) endA1 hsdR17 (rK mK+) relA1 glnV44

JM109 F´traD36 proA+B+ lacIq Δ(lacZ)M15/ Δ(lac-proAB) glnV44 e14- gyrA96 recA1 relA1 endA1 thi hsdR17

JM110 F´ traD36 lacIqΔ(lacZ)M15 proA+B+IrpsL (Strr) thr leu thi lacY galK galT ara fhuA dam dcm glnV44 Δ(lac-proAB)

K802 F e14- (McrA-) lacY1 or Δ(lac)6 glnV44 galK2 galT22 rfbD1 metB1 mcrB1 hsdR2 (rKmK+)

LE392 F e14 (McrA–) hsdR514 (rKmK+) glnV44 supF58 lacY1 or Δ(lacIZY)6 galK2 galT22 metB1 trpR55

MC1061 F araD139 Δ(ara-leu)7696 galE15 galK16 Δ(lac)X74 rpsL (Strr) hsdR2 (rKmK+) mcrA mcrB1

MM294 F endA1 hsdR17 (rKmK+) glnV44 thi-1 relA1 rfbD1 spoT1

NM477 C600 Δ(hsdMS-mcrB)5 (rKmK+ McrBC)

NM522 F´proA+B+ lacIq Δ(lacZ)M15/ Δ(lac-proAB) glnV thi-1 Δ(hsdS-mcrB)5

NM554 MC1061 recA13

NM621 F hsdR (rKmK+) mcrA mcrB glnV44 recD1009

RR1 HB101 RecA+

χ1776 F fhuA53 dapD8 minA1 glnV44 Δ(gal-uvrB)40 minB2 rfb-2 gyrA25 (Nalr) thyA142 oms-2 metC65 oms-1 (tte-1) Δ(bioH-asd)29 cycB2 cycA1 hsdR2 (rK mK+) mcrB1

References

  1. New England Biolabs. E. coli Strain Genotypes. http://www.neb.com/nebecomm/tech_reference/restriction_enzymes/ecoli_genotypes.asp (Oct. 31, 2005)
  2. Wertman, K.F. et al. (1986) Gene 49, 253–262.
  3. Yanisch–Perron, C., Viera, J. and Messing, J. (1985) Gene 33, 103–119.
  4. Sambrook, J., Fritsch, E.F. and Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, (2nd ed.). Cold Spring Harbor: Cold Spring Harbor Laboratory Press.
  5. Huynh,T.V. et al. (1985). In D.M. Glover (Ed.), DNA Cloning Vol. 1, (pp. 56–110). Oxford, England: IRL Press Limited.
  6. Raleigh, E.A. et al. (1988) Nucl. Acids Res. 16, 1563–1575.
  7. Woodcock, D.M. et al. (1989) Nucl. Acids Res. 17, 3469–3478.
  8. Raleigh, E.A., Lech, K. and Brent, R. (1989). In F.M. Ausebel et al. (Eds.), Current Protocols in Molecular Biology (p. 1.4). New York: Publishing Associates and Wiley Interscience.
  9. Berlyn, M.K.B. (1996). In F.C. Niedhardt et al. (Ed.), Escherichia coli and Salmonella: cellular and molecular biology, (2nd ed.), Vol. 2, (pp. 1715–1902). ASM Press.
  10. Miller, J.H. (1972). Experiments in Molecular Genetics. Cold Spring Harbor: Cold Spring Harbor Laboratory Press.
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  12. Murray, N.E. et al. (1977) Mol. Gen. Genet. 150, 53–61.
  13. Palmer, B.R. and Marinus, M.G. (1994) Gene 143, 1–12.
  14. Boyer, H.W, and Roulland–Dussoix, D. (1969) J. Mol. Biol. 41, 459.
  15. Silhavy, T.J. et al. (1984) Experiments with Gene Fusions (pp. xi–xii) Cold Spring Harbor: Cold Spring Harbor Laboratory.
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  17. Maurizi, M.R. et al. (1985) J. Bacteriol. 164, 1124–1135.
  18. Studier, F.W. et al. (1990). In D.V. Goeddel (Ed.), Methods in Enzymology Vol. 185, (pp. 60–89). San Diego: Academic Press.
  19. Kelleher, J. and Raleigh, E.A. (1991) J. Bacteriol. 173, 5220–5223.
  20. Woodcock, D.M. et al. (1989) Nucl. Acids Res. 17, 3469–3478.
  21. Palmer, B.R. and Marinus, M.G. (1994) Gene 143, 1–12.
  22. Yanisch-Perron, C., Viera, J. and Messing, J. (1985) Gene 33, 103–119.
  23. Messing, J. (1979) Recombinant DNA Technical Bulletin (NIH) 2, 43–48.
  24. Gough, J. and Murray, N. (1983) J. Mol. Biol. 166, 1–19.
  25. Baker, T.A. et al. (1984) Proc. Nat. Acad. Sci. USA 81, 6779–6783.
  26. Grossman, A.D. et al. (1983) Cell 32, 151–159
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  32. Kunkel, T.A. et al. (1987). In R. Wu and L. Grossman (Eds.), Methods in Enzymology Vol. 154, (pp. 367–382). San Diego: Academic Press.

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