Difference between revisions of "Part:BBa K3740019"
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<partinfo>BBa_K3740019 short</partinfo> | <partinfo>BBa_K3740019 short</partinfo> | ||
+ | ===Description=== | ||
+ | Near-infrared light activated synthesis of c-di-GMP in <i>Gluconacetobacter hansenii</i> ATCC 53582. | ||
− | + | ===Sequence and Features=== | |
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<partinfo>BBa_K3740019 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3740019 SequenceAndFeatures</partinfo> | ||
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<partinfo>BBa_K3740019 parameters</partinfo> | <partinfo>BBa_K3740019 parameters</partinfo> | ||
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+ | =2021 SZPT-China= | ||
+ | <h3>Biology</h3> | ||
+ | <p>As a photoactivated diguanylate cyclase (DGC), the chimeric protein BphS consists of the N-terminal photosensitive module of the BphG protein from <i>Rhodobacter sphaeroides</i> and the introduction of the R587A mutation into the RXXD motif from the C-terminal GGDEF domain of Slr1143. BphS protein is activated by changes in protein conformation under NIR light irradiation, thereby synthesizing c-di-GMP.</i> | ||
+ | [[File:File.png|200px|thumb|center|Figure 1. Engineering a potent photoactivated DGC]] |
Revision as of 13:16, 18 October 2021
bphS, photo-activated diguanylate cyclase
Description
Near-infrared light activated synthesis of c-di-GMP in Gluconacetobacter hansenii ATCC 53582.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NotI site found at 128
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 233
Illegal BglII site found at 1296
Illegal XhoI site found at 571 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 386
Illegal NgoMIV site found at 560
Illegal NgoMIV site found at 877
Illegal NgoMIV site found at 938 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 921
Illegal BsaI.rc site found at 421
Illegal BsaI.rc site found at 1395
2021 SZPT-China
Biology
As a photoactivated diguanylate cyclase (DGC), the chimeric protein BphS consists of the N-terminal photosensitive module of the BphG protein from Rhodobacter sphaeroides and the introduction of the R587A mutation into the RXXD motif from the C-terminal GGDEF domain of Slr1143. BphS protein is activated by changes in protein conformation under NIR light irradiation, thereby synthesizing c-di-GMP.</i>