Whole-Genome Shotgun Sequencing of Two β-Proteobacterial Species in Search of the Bulgecin Biosynthetic Cluster

被引:21
|
作者
Horsman, Mark E. [1 ]
Marous, Daniel R. [1 ]
Li, Rongfeng [3 ]
Oliver, Ryan A. [3 ]
Byun, Byungjin [1 ]
Emrich, Scott J. [2 ]
Boggess, Bill [1 ]
Townsend, Craig A. [3 ]
Mobashery, Shahriar [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Comp Sci & Engn, Notre Dame, IN 46556 USA
[3] Johns Hopkins Univ, Dept Chem, Charles & 34Th St, Baltimore, MD 21218 USA
基金
美国国家卫生研究院;
关键词
LACTAM ANTIBIOTICS; PSEUDOMONAS-COCOVENENANS; BACTERIAL METABOLITES; IDENTIFICATION; POTENTIATORS; SULFAZECIN; MM-42842; ESKAPE; MEMBER;
D O I
10.1021/acschembio.7b00687
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have-produced draft Whole-genome sequences for two bacterial strains reported to produce the bulgecins as well as NRPS-derived monobactam beta-lactam antibiotics. We propose classification, of ATCC 31363 as Paraburkholderia acidophila. We further reaffirm that ATCC 31433, (Burkholderia ubonensis subsp. mesacidophila) is a taxonomically distinct producer of bulgecins with notable gene regions shared with Paraburkholderia acidophila. We use RAST multiple-gene comparison and MASH distancing with published genomes to order the draft contigs and identify unique gene regions for characterization. Forty-eight natural-product gene clusters are presented from PATRIC (RASTtk) and antiSMASH annotations. We present evidence that the 10 genes that follow the sulfazecin and isosulfazecin pathways in both species are likely involved in bulgecin A biosynthesis.
引用
收藏
页码:2552 / 2557
页数:6
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