Difference between revisions of "Part:BBa K5071010"
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+ | <title>BBa_K5071010 (BGCII-5)</title> | ||
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+ | <h2>Composite part BBa_K5071010 (BGCII-5)</h2> | ||
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+ | <h3>Name: BGCII-5</h3> | ||
+ | <p><strong>Base Pairs:</strong> 1500 bp</p> | ||
+ | <p><strong>Origin:</strong> Paceibacterales</p> | ||
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+ | <h3>Usage and Biology</h3> | ||
+ | <p> | ||
+ | BGCII-5 is a gene identified within a predicted terpene biosynthesis gene cluster, with bioinformatic tools suggesting a potential role in terpene production. Although its precise function remains unknown, sequence analysis indicates the presence of conserved domains common to enzymes involved in secondary metabolite pathways, highlighting its potential importance in the biosynthesis of terpenoids. Further experimental validation is required to elucidate its specific role. | ||
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+ | <h3>Cultivation</h3> | ||
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+ | We used PCR to amplify the BGCII-5 gene, with a length of 1500 bp. Fig 1 shows a band consistent with the target size, indicating that the target gene was successfully amplified. After agarose gel electrophoresis and gel recovery, homologous recombination was used to obtain the recombinant plasmid pRSFuet-BGCII-gene685. | ||
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+ | <img src="https://static.igem.wiki/teams/5071/bba-k5071010/1.jpg" alt="Fig 1. The purpose segment of plasmid pRSFuet-BGCII-gene685"> | ||
+ | <div class="caption">Fig 1. The purpose segment of plasmid pRSFuet-BGCII-gene685</div> | ||
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Latest revision as of 04:52, 30 September 2024
BGCII-5
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 700
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 700
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 700
Illegal BglII site found at 1131 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 700
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 700
- 1000COMPATIBLE WITH RFC[1000]
Composite part BBa_K5071010 (BGCII-5)
Name: BGCII-5
Base Pairs: 1500 bp
Origin: Paceibacterales
Usage and Biology
BGCII-5 is a gene identified within a predicted terpene biosynthesis gene cluster, with bioinformatic tools suggesting a potential role in terpene production. Although its precise function remains unknown, sequence analysis indicates the presence of conserved domains common to enzymes involved in secondary metabolite pathways, highlighting its potential importance in the biosynthesis of terpenoids. Further experimental validation is required to elucidate its specific role.
Cultivation
We used PCR to amplify the BGCII-5 gene, with a length of 1500 bp. Fig 1 shows a band consistent with the target size, indicating that the target gene was successfully amplified. After agarose gel electrophoresis and gel recovery, homologous recombination was used to obtain the recombinant plasmid pRSFuet-BGCII-gene685.