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Insertion sequence IS6100 on plasmid pOAD2, which degrades nylon oligomers
Journal of Bacteriology
|February 1, 1994
Summary
Researchers identified an 880 bp identical sequence in the nylon-degrading plasmid pOAD2, matching the IS6100 insertion sequence. This sequence, found in Flavobacterium sp., also showed homology in Pseudomonas sp. plasmids.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- Nylon oligomer degradation is facilitated by specific bacterial plasmids.
- Plasmid pOAD2 from Flavobacterium sp. strain K172 contains repeated sequence I.
- Insertion sequences (IS) are mobile genetic elements that can influence plasmid structure and function.
Purpose of the Study:
- To determine the nucleotide sequence of repeated sequence I in plasmid pOAD2.
- To compare repeated sequence I with known insertion sequences.
- To investigate the presence of homologous sequences in other nylon-degrading plasmids.
Main Methods:
- DNA sequencing of repeated sequence I from plasmid pOAD2.
- Sequence comparison analysis.
- Southern hybridization experiments.
Main Results:
- Repeated sequence I consists of 880 bp of identical sequence.
- This sequence is identical to IS6100, an insertion sequence from the IS6 family.
- Homologous sequences to IS6100 were detected in the nylon-degrading plasmid pNAD2 from Pseudomonas sp. strain NK87.
Conclusions:
- Repeated sequence I in pOAD2 is an instance of the IS6100 insertion sequence.
- IS6100 is present in plasmids from different bacterial genera involved in nylon degradation.
- This finding suggests horizontal transfer or shared ancestry of IS6100 among nylon-degrading bacteria.