| Application | Comment | Organism |
|---|---|---|
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Haemophilus parainfluenzae |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Brevibacillus brevis |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Lysinibacillus sphaericus |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Acidithiobacillus ferrooxidans |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Geobacillus stearothermophilus |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Acetobacter aceti |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Xanthomonas campestris pv. badrii |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Bergeriella denitrificans |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Neisseria oralis |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Priestia megaterium |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Bacillus amyloliquefaciens |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Xanthomonas campestris |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Pseudomonas fluorescens |
| analysis | measurement of restriction digest efficiency using digital cell-free protein synthesis, which enables a sensitive trace analysis of undigested DNA at the single-molecule level in a PCR-free manner. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Gordonia rubripertincta |
| KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
|---|---|---|---|---|---|
| 0.000027 | - |
linear mNeonGreen DNA | 37°C, pH not specified in the publication | Bergeriella denitrificans |
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Acetobacter aceti | - |
- |
- |
| Acidithiobacillus ferrooxidans | - |
- |
- |
| Bacillus amyloliquefaciens | - |
- |
- |
| Bergeriella denitrificans | - |
- |
- |
| Brevibacillus brevis | - |
- |
- |
| Geobacillus stearothermophilus | Q8KWF1 | - |
- |
| Geobacillus stearothermophilus | Q1PGP7 | - |
- |
| Geobacillus stearothermophilus | E5Q8U2 | - |
- |
| Geobacillus stearothermophilus GR75 | Q1PGP7 | - |
- |
| Gordonia rubripertincta | O85489 | - |
- |
| Haemophilus parainfluenzae | P29537 | - |
- |
| Lysinibacillus sphaericus | - |
- |
- |
| Neisseria oralis | - |
- |
- |
| Priestia megaterium | - |
- |
- |
| Priestia megaterium S2 | - |
- |
- |
| Pseudomonas fluorescens | F1KM53 | - |
- |
| Xanthomonas campestris | G3JXC4 | - |
- |
| Xanthomonas campestris pv. badrii | - |
- |
- |
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| linear mNeonGreen DNA + H2O | - |
Haemophilus parainfluenzae | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Brevibacillus brevis | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Lysinibacillus sphaericus | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Acidithiobacillus ferrooxidans | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Geobacillus stearothermophilus | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Acetobacter aceti | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Xanthomonas campestris pv. badrii | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Bergeriella denitrificans | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Neisseria oralis | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Priestia megaterium | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Bacillus amyloliquefaciens | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Xanthomonas campestris | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Pseudomonas fluorescens | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Gordonia rubripertincta | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Geobacillus stearothermophilus GR75 | ? | - |
? | |
| linear mNeonGreen DNA + H2O | - |
Priestia megaterium S2 | ? | - |
? | |
| additional information | HpaI displays 95.84% digest efficiency by digitial counting and a digest efficiency of 99.4% by Bioanalyzer analysis | Haemophilus parainfluenzae | ? | - |
- |
|
| additional information | BbsI displays 87.35% digest efficiency by digitial counting and a digest efficiency of 91.1% by Bioanalyzer analysis | Brevibacillus brevis | ? | - |
- |
|
| additional information | BsgI displays 94.74% digest efficiency by digitial counting and a digest efficiency of 99.3% by Bioanalyzer analysis | Lysinibacillus sphaericus | ? | - |
- |
|
| additional information | AfeI displays 95.18% digest efficiency by digitial counting | Acidithiobacillus ferrooxidans | ? | - |
- |
|
| additional information | BstXI displays 77.76% digest efficiency by digitial counting and a digest efficiency of 61.5% by Bioanalyzer analysis | Geobacillus stearothermophilus | ? | - |
- |
|
| additional information | StuI displays 93.8% digest efficiency by digitial counting and a digest efficiency of 98.5% by Bioanalyzer analysis | Acetobacter aceti | ? | - |
- |
|
| additional information | BsrGI displays 93.78% digest efficiency by digitial counting and a digest efficiency of 97.7% by Bioanalyzer analysis | Geobacillus stearothermophilus | ? | - |
- |
|
| additional information | XbaI displays 99.25% digest efficiency by digitial counting | Xanthomonas campestris pv. badrii | ? | - |
- |
|
| additional information | NdeI displays 67.12% digest efficiency by digitial counting and a digest efficiency of 59.9% by Bioanalyzer analysis | Bergeriella denitrificans | ? | - |
- |
|
| additional information | NheI displays 96.06% digest efficiency by digitial counting and a digest efficiency of 96.3% by Bioanalyzer analysis | Neisseria oralis | ? | - |
- |
|
| additional information | BmtI displays 73.23% digest efficiency by digitial counting and a digest efficiency of 72.8% by Bioanalyzer analysis | Priestia megaterium | ? | - |
- |
|
| additional information | BamHI displays 98.53% digest efficiency by digitial counting and a digest efficiency of 98.1% by Bioanalyzer analysis | Bacillus amyloliquefaciens | ? | - |
- |
|
| additional information | XcmI displays 98.05% digest efficiency by digitial counting | Xanthomonas campestris | ? | - |
- |
|
| additional information | PflMI displays 96.03% digest efficiency by digitial counting | Pseudomonas fluorescens | ? | - |
- |
|
| additional information | BstEII displays 97.72% digest efficiency by digitial counting and a digest efficiency of 99.2% by Bioanalyzer analysis | Geobacillus stearothermophilus | ? | - |
- |
|
| additional information | NcoI displays 94.42% digest efficiency by digitial counting | Gordonia rubripertincta | ? | - |
- |
|
| additional information | BsrGI displays 93.78% digest efficiency by digitial counting and a digest efficiency of 97.7% by Bioanalyzer analysis | Geobacillus stearothermophilus GR75 | ? | - |
- |
|
| additional information | BmtI displays 73.23% digest efficiency by digitial counting and a digest efficiency of 72.8% by Bioanalyzer analysis | Priestia megaterium S2 | ? | - |
- |
|
| mScarlet DNA + H2O | - |
Haemophilus parainfluenzae | ? | - |
? | |
| mScarlet DNA + H2O | - |
Brevibacillus brevis | ? | - |
? | |
| mScarlet DNA + H2O | - |
Lysinibacillus sphaericus | ? | - |
? | |
| mScarlet DNA + H2O | - |
Acidithiobacillus ferrooxidans | ? | - |
? | |
| mScarlet DNA + H2O | - |
Geobacillus stearothermophilus | ? | - |
? | |
| mScarlet DNA + H2O | - |
Acetobacter aceti | ? | - |
? | |
| mScarlet DNA + H2O | - |
Xanthomonas campestris pv. badrii | ? | - |
? | |
| mScarlet DNA + H2O | - |
Bergeriella denitrificans | ? | - |
? | |
| mScarlet DNA + H2O | - |
Neisseria oralis | ? | - |
? | |
| mScarlet DNA + H2O | - |
Priestia megaterium | ? | - |
? | |
| mScarlet DNA + H2O | - |
Bacillus amyloliquefaciens | ? | - |
? | |
| mScarlet DNA + H2O | - |
Xanthomonas campestris | ? | - |
? | |
| mScarlet DNA + H2O | - |
Pseudomonas fluorescens | ? | - |
? | |
| mScarlet DNA + H2O | - |
Gordonia rubripertincta | ? | - |
? | |
| mScarlet DNA + H2O | - |
Geobacillus stearothermophilus GR75 | ? | - |
? | |
| mScarlet DNA + H2O | - |
Priestia megaterium S2 | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Haemophilus parainfluenzae | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Brevibacillus brevis | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Lysinibacillus sphaericus | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Acidithiobacillus ferrooxidans | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Geobacillus stearothermophilus | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Acetobacter aceti | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Xanthomonas campestris pv. badrii | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Bergeriella denitrificans | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Neisseria oralis | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Priestia megaterium | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Bacillus amyloliquefaciens | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Xanthomonas campestris | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Pseudomonas fluorescens | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Gordonia rubripertincta | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Geobacillus stearothermophilus GR75 | ? | - |
? | |
| mTurquoise2 DNA + H2O | - |
Priestia megaterium S2 | ? | - |
? |
| Synonyms | Comment | Organism |
|---|---|---|
| AfeI | - |
Acidithiobacillus ferrooxidans |
| BamHI | - |
Bacillus amyloliquefaciens |
| BbsI | - |
Brevibacillus brevis |
| BmtI | - |
Priestia megaterium |
| BsgI | - |
Lysinibacillus sphaericus |
| BsrGI | - |
Geobacillus stearothermophilus |
| BstEII | - |
Geobacillus stearothermophilus |
| BstXI | - |
Geobacillus stearothermophilus |
| HpaI | - |
Haemophilus parainfluenzae |
| NcoI | - |
Gordonia rubripertincta |
| NdeI | - |
Bergeriella denitrificans |
| NheI | - |
Neisseria oralis |
| PflMI | - |
Pseudomonas fluorescens |
| StuI | - |
Acetobacter aceti |
| XbaI | - |
Xanthomonas campestris pv. badrii |
| XcmI | - |
Xanthomonas campestris |
| Turnover Number Minimum [1/s] | Turnover Number Maximum [1/s] | Substrate | Comment | Organism | Structure |
|---|---|---|---|---|---|
| 0.0037 | - |
linear mNeonGreen DNA | 37°C, pH not specified in the publication | Bergeriella denitrificans |
| General Information | Comment | Organism |
|---|---|---|
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Haemophilus parainfluenzae |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Brevibacillus brevis |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Lysinibacillus sphaericus |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Acidithiobacillus ferrooxidans |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Geobacillus stearothermophilus |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Acetobacter aceti |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Xanthomonas campestris pv. badrii |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Bergeriella denitrificans |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Neisseria oralis |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Priestia megaterium |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Bacillus amyloliquefaciens |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Xanthomonas campestris |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Pseudomonas fluorescens |
| metabolism | measurement of restriction digest efficiency using digital cell-free protein synthesis. The quantitative measurements reveal a considerable variation in the digest efficiency among restriction endonucleases, from less than 70% to more than 99%. None of them shows truly complete digestion within reasonably long periods of reaction time | Gordonia rubripertincta |