Difference between revisions of "Part:BBa K5071006"

 
 
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BGCII-1
 
  
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===Usage and Biology===
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    <h2>Composite part BBa_K5071006 (BGCII-1)</h2>
  
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    <h3>Name: BGCII-1</h3>
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===Functional Parameters===
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    <p><strong>Base Pairs:</strong> 180 bp</p>
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<partinfo>BBa_K5071006 parameters</partinfo>
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    <p><strong>Origin:</strong> Paceibacterales</p>
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    <h3>Usage and Biology</h3>
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        BGCII-1 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-1 gene, with a length of 180 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 pACYCDuet-BGCII-gene143.
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        <img src="https://static.igem.wiki/teams/5071/bba-k5071006/1.jpg" alt="Fig 1. The purpose segment of plasmid pACYCDuet-BGCII-gene143">
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        <div class="caption">Fig 1. The purpose segment of plasmid pACYCDuet-BGCII-gene143</div>
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Latest revision as of 04:46, 30 September 2024


BGCII-1



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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 73
  • 1000
    COMPATIBLE WITH RFC[1000]

<!DOCTYPE html> BBa_K5071006 (BGCII-1)

Composite part BBa_K5071006 (BGCII-1)

Name: BGCII-1

Base Pairs: 180 bp

Origin: Paceibacterales

Usage and Biology

BGCII-1 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-1 gene, with a length of 180 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 pACYCDuet-BGCII-gene143.

Fig 1. The purpose segment of plasmid pACYCDuet-BGCII-gene143
Fig 1. The purpose segment of plasmid pACYCDuet-BGCII-gene143