Difference between revisions of "Part:BBa K5071013"

 
 
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BGCII-8
 
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===Usage and Biology===
 
  
 
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===Functional Parameters===
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    <h2>Composite part BBa_K5071013 (BGCII-8)</h2>
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    <h3>Name: BGCII-8</h3>
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    <p><strong>Base Pairs:</strong> 350 bp</p>
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    <p><strong>Origin:</strong> Paceibacterales</p>
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    <h3>Usage and Biology</h3>
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        BGCII-8 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-8 gene, with a length of 350 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-k5071013/1.jpg" alt="Fig 1. The purpose segment of plasmid pRSFuet-BGCII-gene685">
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        <div class="caption">Fig 1. The purpose segment of plasmid pRSFuet-BGCII-gene685</div>
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Latest revision as of 05:36, 30 September 2024

BGCII-8


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


BBa_K5071013 (BGCII-8)

Composite part BBa_K5071013 (BGCII-8)

Name: BGCII-8

Base Pairs: 350 bp

Origin: Paceibacterales

Usage and Biology

BGCII-8 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-8 gene, with a length of 350 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.

Fig 1. The purpose segment of plasmid pRSFuet-BGCII-gene685
Fig 1. The purpose segment of plasmid pRSFuet-BGCII-gene685