Part:BBa_K3887001:Design
SttH
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 178
Illegal EcoRI site found at 550
Illegal PstI site found at 337
Illegal PstI site found at 436 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 178
Illegal EcoRI site found at 550
Illegal PstI site found at 337
Illegal PstI site found at 436 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 178
Illegal EcoRI site found at 550
Illegal XhoI site found at 1081 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 178
Illegal EcoRI site found at 550
Illegal PstI site found at 337
Illegal PstI site found at 436 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 178
Illegal EcoRI site found at 550
Illegal PstI site found at 337
Illegal PstI site found at 436
Illegal NgoMIV site found at 210
Illegal NgoMIV site found at 468
Illegal NgoMIV site found at 1171
Illegal NgoMIV site found at 1437
Illegal AgeI site found at 356
Illegal AgeI site found at 697 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
SttH is an enzyme from Streptomyces toxytricini used during the conversion of indole. In our experiment, SttH and TnaA to convert Trp to 6-Br-Trp, then to 6-Br-indole. The strength of SttH is it shows strict regiospecificity for both bromination and chlorination. This made it suitable for the bromination of indole. However, SttH alone shows low reactivity and exists insoluble form, so it was expressed with Fre to increase the conversion of Trp to 6-Br-Trp.
Experiment shows by using 2.5mM of indole or Trp, 0.29mM of 6-Br-indole or 0.78mM of 6-Br-Trp is produced, respectively. SttH is 2.5 times more active toward Trp than to indole. So, the SttH reaction from Trp to 6-Br-Trp is followed by TnaA converting 6-Br-Trp to 6-Br-indole.
Source
Trp 6-halogenase from Streptomyces toxytricini (SttH)