Difference between revisions of "Part:BBa K3239005"
BrianSebZhou (Talk | contribs) m (→Usage and Biology) |
Nicole Guo (Talk | contribs) |
||
Line 3: | Line 3: | ||
<partinfo>BBa_K3239005 short</partinfo> | <partinfo>BBa_K3239005 short</partinfo> | ||
− | Transcription factor in the P. pastoris GS115 strain. Self-upregulates | + | Transcription factor in the ''P. pastoris GS115'' strain. Self-upregulates ''PRM1'' expression and upregulates ''MIT1'' and ''AOX1'' expression. |
===Usage and Biology=== | ===Usage and Biology=== | ||
− | The Prm1 transcription factor is homogeneous to the P. pastoris GS115 strain and is critical in the regulation of AOX1 (alcohol oxidase) expression in the methylotrophic yeast. Upon methanol induction, the Mxr1 | + | The Prm1 transcription factor is homogeneous to the ''P. pastoris GS115'' strain and is critical in the regulation of ''AOX1'' (alcohol oxidase 1) expression in the methylotrophic yeast. Upon methanol induction, the Mxr1 transcription factor is expressed and the ''PRM1'' promoter (''P<sub>PRM1'') is activated. Mxr1 derepresses the ''AOX1'' promoter (''P<sub>AOX1''), whereas the Prm1 protein not only self-upregulates but also upregulates the expression of the ''MIT1'' gene. Prm1 and Mit1 both upregulate ''AOX1'' expression, allowing the yeast to rapidly produce enough alcohol oxidase 1 to metabolize methanol. Mit1 however, also downregulates the expression of ''PRM1'', inhibiting the over-activation of ''P<sub>PRM1'', ''P<sub>MIT1'' and ''P<sub>AOX1''. |
===Functional Parameters=== | ===Functional Parameters=== |
Revision as of 06:10, 18 October 2019
Prm1 transcription factor in the P.pastoris GS115 strain
Transcription factor in the P. pastoris GS115 strain. Self-upregulates PRM1 expression and upregulates MIT1 and AOX1 expression.
Usage and Biology
The Prm1 transcription factor is homogeneous to the P. pastoris GS115 strain and is critical in the regulation of AOX1 (alcohol oxidase 1) expression in the methylotrophic yeast. Upon methanol induction, the Mxr1 transcription factor is expressed and the PRM1 promoter (PPRM1) is activated. Mxr1 derepresses the AOX1 promoter (PAOX1), whereas the Prm1 protein not only self-upregulates but also upregulates the expression of the MIT1 gene. Prm1 and Mit1 both upregulate AOX1 expression, allowing the yeast to rapidly produce enough alcohol oxidase 1 to metabolize methanol. Mit1 however, also downregulates the expression of PRM1, inhibiting the over-activation of PPRM1, PMIT1 and PAOX1.
Functional Parameters
A single-base mutation is introduced for compatibility with Type IIS. This single mutation does not affect the protein sequence.
Reference
Liang, S., Wang, B., Pan, L., Ye, Y., He, M., Han, S., … Lin, Y. (2012). Comprehensive structural annotation of Pichia pastoris transcriptome and the response to various carbon sources using deep paired-end RNA sequencing. BMC Genomics, 13(1). https://doi.org/10.1186/1471-2164-13-738
Shi, L., Wang, J., Wang, X., Zhang, Y., Song, Z., Cai, M., & Zhou, X. (2019). Transcriptome and metabolome analyses reveal global behaviour of a genetically engineered methanol-independent Pichia pastoris strain. Process Biochemistry, 76(August 2018), 46–54. https://doi.org/10.1016/j.procbio.2018.10.014
Wang, X., Wang, Q., Wang, J., Zhou, M., Shi, L., Zhou, X., … Shen, W. (2016). Mit1 Transcription Factor Mediates Methanol Signaling and Regulates the Alcohol Oxidase 1 ( AOX1 ) Promoter in Pichia pastoris. Journal of Biological Chemistry, 291(12), 6245–6261. https://doi.org/10.1074/jbc.m115.692053
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1034
Illegal PstI site found at 1556 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1034
Illegal NheI site found at 2815
Illegal PstI site found at 1556 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1034
Illegal BglII site found at 387
Illegal BamHI site found at 1917
Illegal BamHI site found at 2836 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1034
Illegal PstI site found at 1556 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1034
Illegal PstI site found at 1556 - 1000COMPATIBLE WITH RFC[1000]