2009
DOI: 10.1002/cbic.200900297
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Identifying Natural Product Biosynthetic Genes from a Soil Metagenome by Using T7 Phage Selection

Abstract: Doing the dirty work: Metagenomic DNA was directly isolated from soil bacteria to construct a T7 phage library. Iterative phage selection by protein modification catalyzed by phosphopantetheinyl transferase enriched putative acyl carrier protein and peptidyl carrier protein genes that are associated with natural product biosynthetic enzymes.

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Cited by 16 publications
(12 citation statements)
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“…Similar trends, in terms of relative differences, have been found for other soil samples (Castañeda & Barbosa, 2017). The higher differences in terms of relative abundance (1.1%) were found for the eggNOG category "Replication, recombination and repair", (which were also over-represented in Cq+Da) to fill gaps and complete the recombination process (Zhang et al, 2009). Insertion of a transposon in a certain genomic position may change underlying DNA sequences, subsequently activating or inactivating gene expression which ultimately may have an impact on their hosts' fitness (Aziz et al, 2010).…”
Section: Discussionsupporting
confidence: 75%
“…Similar trends, in terms of relative differences, have been found for other soil samples (Castañeda & Barbosa, 2017). The higher differences in terms of relative abundance (1.1%) were found for the eggNOG category "Replication, recombination and repair", (which were also over-represented in Cq+Da) to fill gaps and complete the recombination process (Zhang et al, 2009). Insertion of a transposon in a certain genomic position may change underlying DNA sequences, subsequently activating or inactivating gene expression which ultimately may have an impact on their hosts' fitness (Aziz et al, 2010).…”
Section: Discussionsupporting
confidence: 75%
“…Microorganisms are considered to be the best indicators, due to their function, ubiquitous presence, and high sensitivity to pollutant stress (Andreoni et al, 2004;Abd Elsalam et al, 2006). However, as more than 99% of soil microorganisms cannot be cultivated by traditional laboratory techniques (Baker et al, 2001;Zhang et al, 2009a;Lee et al, 2010), culture-independent molecular techniques, such as denaturing gradient gel electrophoresis (DGGE), were developed to obtain both quantitative and qualitative microbial data in the respective environments (Ueno et al, 2001;Lee et al, 2010). The DGGE method has been widely applied to characterize microbial community shifts and to identify the affiliations of microbial populations affected by heavy metals, pesticides, polycyclic aromatic hydrocarbons (PAHs), and other pollutants in the soil (Andreoni et al, 2004;Wang et al, 2007;Wang et al, 2008;Zhang et al, 2009b).…”
Section: Introductionmentioning
confidence: 99%
“…Enzyme activities unique to secondary metabolism can be harnessed to greatly improve the efficiency of identifying eDNA clones with functional biosynthetic gene pathways for downstream phenotypic screens. Required for the posttranslational activation of NRPSs and PKSs, PPTases were harnessed in a phage display study to recover NRPS and PKS sequences from environmental samples [100]. By coupling pigment production or cellular growth to PPTase function, complementation of PPTase activity can be used to screen or select for eDNA clones that contain PKS and/or NRPS gene clusters [87, 101].…”
Section: Metagenomics-driven Drug Discoverymentioning
confidence: 99%