PCRISPomyces-2: Difference between revisions

From ActinoBase
No edit summary
Line 6: Line 6:


This plasmid has been successfully used for genome editing in the following organisms
This plasmid has been successfully used for genome editing in the following organisms
*<em>[[Streptomyces albidoflavus]]</em><sup>2</sup>
*<em>[[Actinoplanes]]</em> sp. SE50/110</em><sup>2</sup>
*<em>[[Streptomyces albidoflavus]]</em><sup>3</sup>
*<em>[[Streptomyces coelicolor]]</em> (unpulished mutagenesis performed within the group of [https://people.uea.ac.uk/m_hutchings Prof Matt Hutchings])
*<em>[[Streptomyces coelicolor]]</em> (unpulished mutagenesis performed within the group of [https://people.uea.ac.uk/m_hutchings Prof Matt Hutchings])
*<em>[[Streptomyces formicae]]</em><sup>3</sup>
*<em>[[Streptomyces formicae]]</em><sup>4</sup>
*<em>[[Streptomyces lividans]]</em><sup>1</sup>
*<em>[[Streptomyces lividans]]</em><sup>1</sup>
*<em>[[Streptomyces roseosporus]]</em></em><sup>4</sup>
*<em>[[Streptomyces rimosus]]</em></em></em><sup>5</sup>
*<em>[[Streptomyces venezuelae]]</em></em><sup>4</sup>
*<em>[[Streptomyces roseosporus]]</em></em><sup>6</sup>
<em>[[Streptomyces showdoensis]]</em><sup>7</sup>
*<em>[[Streptomyces venezuelae]]</em></em><sup>6</sup>
*<em>[[Streptomyces viridochromogenes]]</em></em><sup>1</sup>
*<em>[[Streptomyces viridochromogenes]]</em></em><sup>1</sup>


Line 42: Line 45:
==References==
==References==
#Cobb R.E., Wang, Y., Zhao, H. (2014). High-Efficiency Multiplex Genome Editing of Streptomyces Species Using an Engineered CRISPR/Cas System. ''ACS Synthetic Biology'', 4(6), pp. 723-728. DOI: 10.1021/sb500351f
#Cobb R.E., Wang, Y., Zhao, H. (2014). High-Efficiency Multiplex Genome Editing of Streptomyces Species Using an Engineered CRISPR/Cas System. ''ACS Synthetic Biology'', 4(6), pp. 723-728. DOI: 10.1021/sb500351f
#Wolf, T., Gren, T., Thieme, E., Wibberg, D., Zemke, T., P&uuml;hler, A., Kalinowski, J. (2016). Targeted genome editing in the rare actinomycete Actinoplanes sp. SE50/110 by using the CRISPR/Cas9 System. ''Journal of Biotechnology'', 231, pp. 122-128. DOI: 10.1016/j.jbiotec.2016.05.039.
#McLean, T.C., Hoskisson, P.A., Seipke, R.F. (2016). Coordinate Regulation of Antimycin and Candicidin Biosynthesis. ''mSphere'', 1(6), pp. e00305-e00316. DOI: 10.1128/mSphere.00305-16.
#McLean, T.C., Hoskisson, P.A., Seipke, R.F. (2016). Coordinate Regulation of Antimycin and Candicidin Biosynthesis. ''mSphere'', 1(6), pp. e00305-e00316. DOI: 10.1128/mSphere.00305-16.
#Qin, Z., Munnoch, J.T., Devine R., Holmes, N.A., Seipke, R.F., Wilkinson, K.A., Wilkinson., Hutchings, M.H. (2017). Formicamycins, antibacterial polyketides produced by Streptomyces formicae isolated from African Tetraponera plant-ants. ''Chemical Science'', 8, pp. 3218-3227. DOI: 10.1039/c6sc04265a
#Qin, Z., Munnoch, J.T., Devine R., Holmes, N.A., Seipke, R.F., Wilkinson, K.A., Wilkinson., Hutchings, M.H. (2017). Formicamycins, antibacterial polyketides produced by Streptomyces formicae isolated from African Tetraponera plant-ants. ''Chemical Science'', 8, pp. 3218-3227. DOI: 10.1039/c6sc04265aT
#Jia, H., Zhang, L., Wang, T., Han, J., Tang, H., Zhang, L. (2017). Development of a CRISPR/Cas9-mediated gene-editing tool in Streptomyces rimosus. ''Microbiology'', 163(8), pp. 1148-1155. DOI: 10.1099/mic.0.000501.
#Zhang, M.M., Wong, F.T., Wang, Y., Luo, S., Lim, Y.H., Heng, H., Yeo, W.L., Cobb, R.E., Enghiad, B., Ang, E.L., Zhao, H. (2017). Crispr–Cas9 strategy for activation of silent Streptomyces biosynthetic gene clusters. ''Nature Chemical Biology'', 13, pp. 607-609. DOI: 10.1038/nchembio.2341
#Zhang, M.M., Wong, F.T., Wang, Y., Luo, S., Lim, Y.H., Heng, H., Yeo, W.L., Cobb, R.E., Enghiad, B., Ang, E.L., Zhao, H. (2017). Crispr–Cas9 strategy for activation of silent Streptomyces biosynthetic gene clusters. ''Nature Chemical Biology'', 13, pp. 607-609. DOI: 10.1038/nchembio.2341
#Palmu, K., Rosenqvist, P., Thapa, K., Illina, Y., Siitonen, V., Baral, B., M&auml;kinen, J., Belogurov., Virta, P., Niemi, J., Mets&auml;-Ketel&auml;, M. (2017). Discovery of the Showdomycin Gene Cluster from Streptomyces showdoensis ATCC 15227 Yields Insight into the Biosynthetic Logic of C-Nucleoside Antibiotics. ''ACS Chemical Biology'', 12(6), pp. 1472-1477. DOI: 10.1021/acschembio.7b00078.

Revision as of 14:20, 9 August 2019


Use

This plasmid can be used for precise CRISPR/Cas9-mediated genome engineering of Streptomyces strains1. It is possible to introduce mutations that range from 1-100kbp deletions, precise single base codon changes to alter amino acids and insertions to add Flag-tags to proteins encoded at their native loci.

This plasmid has been successfully used for genome editing in the following organisms

Streptomyces showdoensis7


See here for the original pCRISPomyces2 paper from Cobb et. al1.

Click here for the CRISPR protocol used by Matt Hutchings lab (courtesy of Rebecca Devine) - or download the PDF.

Features

  • Ampicillin resistance cassette
  • Origin of conjugative transfer (oriT)
  • Origin of replication for Escherichia coli (pBR322oriF)
  • Codon optomised cas9 gene under the constitutive rpSL promoter
  • LacZ cassette for golden gate cloning of guide RNA (gRNA)
  • Constitutive gapdh promoter for gRNA expression
  • pSG5 temparature sensitive Streptomyces origin of replication. Without selection and above 37°C the plasmid becomes unstable. This property is used to cure the plasmid from Streptomyces after successful mutagenesis.
  • Xba1 site for gibson assembly of repair templates

History

The plasmid was made by Huimin Zhao's group and is available free from AddGene under MTA: click here

Map

PCRISPomyces-2 map.png


Sequence links

AddGene under MTA: click here

References

  1. Cobb R.E., Wang, Y., Zhao, H. (2014). High-Efficiency Multiplex Genome Editing of Streptomyces Species Using an Engineered CRISPR/Cas System. ACS Synthetic Biology, 4(6), pp. 723-728. DOI: 10.1021/sb500351f
  2. Wolf, T., Gren, T., Thieme, E., Wibberg, D., Zemke, T., Pühler, A., Kalinowski, J. (2016). Targeted genome editing in the rare actinomycete Actinoplanes sp. SE50/110 by using the CRISPR/Cas9 System. Journal of Biotechnology, 231, pp. 122-128. DOI: 10.1016/j.jbiotec.2016.05.039.
  3. McLean, T.C., Hoskisson, P.A., Seipke, R.F. (2016). Coordinate Regulation of Antimycin and Candicidin Biosynthesis. mSphere, 1(6), pp. e00305-e00316. DOI: 10.1128/mSphere.00305-16.
  4. Qin, Z., Munnoch, J.T., Devine R., Holmes, N.A., Seipke, R.F., Wilkinson, K.A., Wilkinson., Hutchings, M.H. (2017). Formicamycins, antibacterial polyketides produced by Streptomyces formicae isolated from African Tetraponera plant-ants. Chemical Science, 8, pp. 3218-3227. DOI: 10.1039/c6sc04265aT
  5. Jia, H., Zhang, L., Wang, T., Han, J., Tang, H., Zhang, L. (2017). Development of a CRISPR/Cas9-mediated gene-editing tool in Streptomyces rimosus. Microbiology, 163(8), pp. 1148-1155. DOI: 10.1099/mic.0.000501.
  6. Zhang, M.M., Wong, F.T., Wang, Y., Luo, S., Lim, Y.H., Heng, H., Yeo, W.L., Cobb, R.E., Enghiad, B., Ang, E.L., Zhao, H. (2017). Crispr–Cas9 strategy for activation of silent Streptomyces biosynthetic gene clusters. Nature Chemical Biology, 13, pp. 607-609. DOI: 10.1038/nchembio.2341
  7. Palmu, K., Rosenqvist, P., Thapa, K., Illina, Y., Siitonen, V., Baral, B., Mäkinen, J., Belogurov., Virta, P., Niemi, J., Metsä-Ketelä, M. (2017). Discovery of the Showdomycin Gene Cluster from Streptomyces showdoensis ATCC 15227 Yields Insight into the Biosynthetic Logic of C-Nucleoside Antibiotics. ACS Chemical Biology, 12(6), pp. 1472-1477. DOI: 10.1021/acschembio.7b00078.