Journal: mSystems
Article Title: Preparation of functional metagenomic libraries from low biomass samples using METa assembly and their application to capture antibiotic resistance genes
doi: 10.1128/msystems.01039-25
Figure Lengend Snippet: Functional metagenomics and METa assembly. (A) The general steps in the preparation and application of a functional metagenomic library consist of the following. (1) Extraction of metagenomic DNA from a source microbiome. (2) Fragmentation of metagenomic DNA to the preferred size range. (3) Packaging of inserts into expression vectors. (4) Transformation of host cells with vector library. (5) Screen or selection of a functional metagenomic library for a phenotype of interest. (6) Collection of screened or selected metagenomic fragments. (7) Sequencing of selected inserts. (8) Open reading frame calling and annotation to identify potential genes underlying phenotypes of interest. (B) Steps 2 and 3 above are modified in Mosaic ends tagmentation (METa) assembly. Fragmentation is achieved using Tn5 transposase tagmentation with mosaic end sequence oligos. Tagmented DNA is gap-filled by polymerase and directly cloned (without amplification) into an expression vector with matching mosaic end sequences defining the cloning site using assembly cloning.
Article Snippet: The ZymoBIOMICS fecal standard, the source of our stool functional metagenomic library input DNA, has been sequenced and annotated for known antibiotic resistance genes by the Zymo corporation, but the data associated with this product do not list any known streptothricin resistance genes.
Techniques: Functional Assay, Extraction, Expressing, Transformation Assay, Plasmid Preparation, Selection, Sequencing, Modification, Clone Assay, Amplification, Cloning