Difference between revisions of "Part:BBa K2992002"
m (→Characterisation) |
JacobGausden (Talk | contribs) (→Characterisation) |
||
(4 intermediate revisions by 3 users not shown) | |||
Line 3: | Line 3: | ||
<partinfo>BBa_K2992002 short</partinfo> | <partinfo>BBa_K2992002 short</partinfo> | ||
− | <i>botR</i> encodes | + | <i>botR</i> encodes an alternative sigma factor associated with the expression of <i>C. botulinum</i> neurotoxin production genes. |
===Usage and Biology=== | ===Usage and Biology=== | ||
− | BotR regulates the the expression of boutlinum neruotoxin and non-toxic associated proteins during the late exponential and early stationary growth phases. We have integrated <i>botR</i> into the genome of <i>C. sporogenes</i> to generate a reporter strain to validate the concept of using | + | BotR regulates the the expression of boutlinum neruotoxin and non-toxic associated proteins during the late exponential and early stationary growth phases. We have integrated <i>botR</i> into the genome of <i>C. sporogenes</i> to generate a reporter strain to validate the concept of using suitable reporters to predict the production of botulinum neurotoxin following food manufacturing processes. <br><br> |
===Characterisation=== | ===Characterisation=== | ||
− | We made three <i>BotR</i>-expression modules comprising of the <i> | + | This basic part was used in many experiments to produce the sigma factor, responsible for the the expression of acetone, GusA or FAST when placed downstream of a BoTR-activated promoter. |
+ | We made three <i>BotR</i>-expression modules comprising of the <i>botR</i> sigma factor gene under the control of the native <i>botR</i> promoter, an inducible system and one with no promoter. See our [https://2019.igem.org/Team:Nottingham/Results results page] for more information. | ||
+ | |||
Latest revision as of 00:36, 22 October 2019
botR gene from C. botulinum
botR encodes an alternative sigma factor associated with the expression of C. botulinum neurotoxin production genes.
Usage and Biology
BotR regulates the the expression of boutlinum neruotoxin and non-toxic associated proteins during the late exponential and early stationary growth phases. We have integrated botR into the genome of C. sporogenes to generate a reporter strain to validate the concept of using suitable reporters to predict the production of botulinum neurotoxin following food manufacturing processes.
Characterisation
This basic part was used in many experiments to produce the sigma factor, responsible for the the expression of acetone, GusA or FAST when placed downstream of a BoTR-activated promoter. We made three BotR-expression modules comprising of the botR sigma factor gene under the control of the native botR promoter, an inducible system and one with no promoter. See our results page for more information.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
References
Raffestin, S., Dupuy, B., Marvaud, J. and Popoff, M. (2004). BotR/A and TetR are alternative RNA polymerase sigma factors controlling the expression of the neurotoxin and associated protein genes in Clostridium botulinum type A and Clostridium tetani. Molecular Microbiology, 55(1), pp.235-249.
Zhang, Z., Korkeala, H., Dahlsten, E., Sahala, E., Heap, J., Minton, N. and Lindström, M. (2013). Two-Component Signal Transduction System CBO0787/CBO0786 Represses Transcription from Botulinum Neurotoxin Promoters in Clostridium botulinum ATCC 3502. PLoS Pathogens, 9(3), p.e1003252.