Difference between revisions of "Part:BBa K4895996"
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as their one, circularized chromosome is relatively simple to recombine with. While recombination events may be rare, it is often that this low statistical probability can be circumvented with higher efficiency transformations as well as higher quality transformants. However, in the past, recombination often requires a separate bacterium along with a full expression plasmid. For instance, it is commonplace to create a full plasmid that includes an origin of replication that may not be compatible with the targeted strain of bacteria, as a way of easily cloning the plasmid and repairing any nicks in a separate cloning step. It is understandable that using a different strain or even species of bacteria can be daunting, and generating or buying a full plasmid can be pricey. Along with this, the old method of recombination requires two recombination sites, each around 300bp long. Recombination events are rare enough, and adding on the need to generate two recombination events only makes things worse. Fortunately, ASU iGEM has the solution: | as their one, circularized chromosome is relatively simple to recombine with. While recombination events may be rare, it is often that this low statistical probability can be circumvented with higher efficiency transformations as well as higher quality transformants. However, in the past, recombination often requires a separate bacterium along with a full expression plasmid. For instance, it is commonplace to create a full plasmid that includes an origin of replication that may not be compatible with the targeted strain of bacteria, as a way of easily cloning the plasmid and repairing any nicks in a separate cloning step. It is understandable that using a different strain or even species of bacteria can be daunting, and generating or buying a full plasmid can be pricey. Along with this, the old method of recombination requires two recombination sites, each around 300bp long. Recombination events are rare enough, and adding on the need to generate two recombination events only makes things worse. Fortunately, ASU iGEM has the solution: | ||
| − | <h3>Introducing: | + | <h3>Introducing: MiKOP, or Micro Knock Out Plasmid</h3> |
| − | This year, we have inadvertently produced a novel technique that is both more accessible and relatively simple to design and build with. However, it must be stressed that this KO technique only applies to genes that are directly downstream of promoter regions, as well as genes that are not polycistronically expressed with vital genes. With that out of the way, let's begin. The design of an | + | This year, we have inadvertently produced a novel technique that is both more accessible and relatively simple to design and build with. However, it must be stressed that this KO technique only applies to genes that are directly downstream of promoter regions, as well as genes that are not polycistronically expressed with vital genes. With that out of the way, let's begin. The design of an MiKOP is very simple, with only 4 major parts: |
<ol> | <ol> | ||
<li>600+bp recombination site</li> | <li>600+bp recombination site</li> | ||
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===Functional Parameters=== | ===Functional Parameters=== | ||
<partinfo>BBa_K4895996 parameters</partinfo> | <partinfo>BBa_K4895996 parameters</partinfo> | ||
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Latest revision as of 20:51, 11 October 2023
Micro-Knock-Out-Plasmid Insert 1
This part is to serve as a template for designing and integrating you own micro-plasmid Knock Out.
Knock Out Plasmids
Often, teams may seek to knock out genomic expression of specific enzymes or regulatory sequences in bacteria, as their one, circularized chromosome is relatively simple to recombine with. While recombination events may be rare, it is often that this low statistical probability can be circumvented with higher efficiency transformations as well as higher quality transformants. However, in the past, recombination often requires a separate bacterium along with a full expression plasmid. For instance, it is commonplace to create a full plasmid that includes an origin of replication that may not be compatible with the targeted strain of bacteria, as a way of easily cloning the plasmid and repairing any nicks in a separate cloning step. It is understandable that using a different strain or even species of bacteria can be daunting, and generating or buying a full plasmid can be pricey. Along with this, the old method of recombination requires two recombination sites, each around 300bp long. Recombination events are rare enough, and adding on the need to generate two recombination events only makes things worse. Fortunately, ASU iGEM has the solution:
Introducing: MiKOP, or Micro Knock Out Plasmid
This year, we have inadvertently produced a novel technique that is both more accessible and relatively simple to design and build with. However, it must be stressed that this KO technique only applies to genes that are directly downstream of promoter regions, as well as genes that are not polycistronically expressed with vital genes. With that out of the way, let's begin. The design of an MiKOP is very simple, with only 4 major parts:
- 600+bp recombination site
- 2 constitutive terminators, upstream of the recombination site
- Antibiotic resistance, upstream of the two terminators
- Constitutive promoter, upstream of the antibiotic resistance, and facing away from the recombination site.
The rationale here is simple: Why use a separate organism for plasmid repair and cloning when it is possible to be done in vitro. The microplasmid takes a bare-bones approach to the KO gene problem. The 600bp recombination site is to increase the chances of recombination, as well as increase the specificity of the recombination site. The 2 constitutive terminators serve as the "KO" mechanism; because we are inserting directly between the gene and its promoter, we know that by inserting two terminators, it definitively shuts down gene expression. Finally, the antibiotic resistance and constitutive promoter serve as a selection mechanism; it is a way of directly confirming the success of the recombination without needing to sequence genomically en masse.
How to use this part
This part serves as a template for designing inserts to be synthesized from either IDT or Twist; the idea is that only the end vision needs to be preserved, as long as the annealing regions lie in non-promoter/terminator regions. Try to avoid overhangs in regions with hairpins
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]