Difference between revisions of "Part:BBa K5034201"
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===Sequence and Features=== | ===Sequence and Features=== | ||
<partinfo>BBa_K5034201 SequenceAndFeatures</partinfo> | <partinfo>BBa_K5034201 SequenceAndFeatures</partinfo> | ||
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+ | ===Experimental Characterization and results=== | ||
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+ | <div align="center"> | ||
+ | <img style="width:50%;height:auto;" src="https://static.igem.wiki/teams/5034/results/fig23.jpg"> | ||
+ | <p> | ||
+ | Figure 1: Fragment obtained by double enzyme digestion of plasmid backbone | ||
+ | </div> | ||
+ | </html> | ||
===Applications=== | ===Applications=== | ||
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===Reference=== | ===Reference=== | ||
− | + | <i>1. Kovach ME, Elzer PH, Hill DS, Robertson GT, Farris MA, Roop RM 2nd, Peterson KM. Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene. 1995 Dec 1;166(1):175-6. doi: 10.1016/0378-1119(95)00584-1. PMID: 8529885.</i> |
Revision as of 06:59, 2 October 2024
pBBR1MCS-terminator plasmid
Contents
Description
The pBBR1MCS plasmid is a synthetic plasmid backbone used in various genetic engineering applications in microbial systems. We modified the original pBBR1MCS and added a double terminator rrnBT1-T7Te(BBa_B0015) downstream the Biobrick suffix.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 4981
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 2834
Illegal NotI site found at 4987 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 4981
Illegal BglII site found at 3580 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found at 4981
Illegal suffix found at 2 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found at 4981
Plasmid lacks a suffix.
Illegal XbaI site found at 4996
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NgoMIV site found at 562
Illegal NgoMIV site found at 4244
Illegal NgoMIV site found at 4527
Illegal AgeI site found at 402 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Experimental Characterization and results
Figure 1: Fragment obtained by double enzyme digestion of plasmid backbone
Applications
1. It can be used in microbial fuel cells to study and enhance the extracellular electron transfer capabilities such as in S. oneidensis.
2. It can be used as a backbone for CRISPR-based genome editing systems, enabling precise genetic modifications.
Reference
1. Kovach ME, Elzer PH, Hill DS, Robertson GT, Farris MA, Roop RM 2nd, Peterson KM. Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene. 1995 Dec 1;166(1):175-6. doi: 10.1016/0378-1119(95)00584-1. PMID: 8529885.