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XJ Autolysis™ E. coli Strains
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Fast-Track transformation procedure with transformation efficiencies of 108 -109 transformants/µg of plasmid DNA. |
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Simple and controlled autolysis of E. coli. |
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XJ Autolysis™ E. coli can by lysed in minutes following isolation. |
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Lysis procedure is compatible with most buffer systems. |
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Simplifies protein expression and purification procedures, also applicable for extraction of nucleic acids. |
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Easy scale-up for the lysis of multiple samples and larger sample volumes. |
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Derived from popular strains:
XJa - JM109 Origin
XJb - BL21 Origin |
| STRAIN GENOTYPES |
| XJa Autolysis™ |
E. coli K recA1 supE44 endA1 hsdR17 (rk-,mk+) gyrA96 relA1 thi mcrA Δ(lac-proAB) ΔaraB::λR, cat F’[traD36 proAB+ lacIq lacZΔM15] |
| XJb Autolysis™ |
E. coli B F- ompT hsdSB(rB- mB-) gal dcm ΔaraB::λR, cat |
The use of XJ Autolysis™ E. coli strains offers a new alternative to current methods for bacterial transformation and bacterial cell lysis. XJ Autolysis™ E. coli strains are efficiently lysed following arabinose induced expression of the bacteriophage lambda lysozyme (i.e., endolysin) protein coupled to a single freeze-thaw cycle. Lysis is quick, reproducible, and simpler compared to current lysis methods. XJ Autolysis™ E. coli strains are suitable to accomodate processing of multiple samples as well as scaling up to larger sampling volumes.
Zymo Research offers a range of chemically competent strains of E. coli having transformation efficiencies >108 transformants/µg pUC19 DNA. With the needs of the researcher in mind, the scientists at Zymo Research developed a unique method to make E. coli stains chemically competent and avoid the requirement of heat-shocking and related procedures. This dramatically reduces processing time, and, in most instances the entire procedure is complete in 10-20 minutes bypassing the need for a lengthy outgrowth period. For transformation, simply mix DNA with competent cells, incubate on ice 10-20 minutes, and spread onto a selection plate.
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XJa Autolysis™
(E. coli K, strain JM109) |
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XJb Autolysis™
(E. coli B, strain BL21) |
| Cell Growth |
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Grows quite well, especially when media is supplemented with 1 mM magnesium. |
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A very robust strain, reaching higher OD’s than E. coli K. |
| Autolysis |
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This strain lyses very easily. Actually, the parent strain JM109 itself will release about 20% of cellular protein after one freeze-thaw cycle. This strain will lyse in a wide range of buffer conditions. |
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XJb lysis efficiency is 10-20 % lower compared to XJa. To achieve optimal lysis, more care needs to be taken when selecting lysis buffer. However, even very low concentrations of a detergent improve lysis significantly. |
| Protein Expression |
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Suitable for general screening, but proteases may degrade the recombinant proteins, especially small or otherwise unstable proteins. |
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Higher protein yields are usually obtained using this strain. XJb is also deficient in both Lon and OmpT proteases, making it especially suitable for recombinant protein expression. |
| DNA Extraction |
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This strain is EndA negative and thus yielding high quality DNA preparations. |
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XJb is not the best strain for DNA extraction. If necessary to do so, techniques should be chosen that yield highly purified DNA in the least amount of time. |
| DNA Stability |
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The RecA negative mutation in XJa stabilizes repetitive DNA sequences. |
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This strain is RecA positive. |

| Product |
Catalog No. |
Format |
Price |
Store |
| XJa Autolysis™ |
T5021 |
1 glycerol stock
1 ml 500X L-Arabinose |
$
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T3021 |
10x 100 µl Z-competent cells
1 ml 500X L-Arabinose |
$
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| XJb Autolysis™ |
T5041 |
1 glycerol stock
1 ml 500X L-Arabinose |
$
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T3041 |
10x 100 µl Z-competent cells
1 ml 500X L-Arabinose |
$
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| Components Available
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