Cloacaenodin, an Antimicrobial Lasso Peptide with Activity against

被引:10
|
作者
Carson, Drew V. [1 ]
Patino, Monica [1 ]
Elashal, Hader E. [1 ]
Cartagena, Alexis Jaramillo [2 ]
Zhang, Yi [1 ]
Whitley, Megan E. [1 ]
So, Larry [1 ]
Kayser-Browne, Angelo K. [1 ]
Earl, Ashlee M. [2 ]
Bhattacharyya, Roby P. [2 ,3 ]
Link, A. . James [1 ,4 ,5 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[2] Broad Inst MIT & Harvard, Infect Dis & Microbiome Program, Cambridge, MA 02142 USA
[3] Massachusetts Gen Hosp, Dept Med, Infect Dis Div, Boston, MA 02114 USA
[4] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
[5] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
来源
ACS INFECTIOUS DISEASES | 2023年 / 9卷 / 01期
基金
美国国家卫生研究院;
关键词
cloacaenodin; genome mining; antimicrobial lasso peptide; Enterobacter cloacae; RiPPs; carbapenem-resistant Enterobacterales; MICROCIN J25; ENTEROBACTER-CLOACAE; RNA-POLYMERASE; SEQUENCE-ANALYSIS; GENOME SEQUENCE; I-III; COLISTIN; STABILITY; TRANSCRIPTION; BIOSYNTHESIS;
D O I
10.1021/acsinfecdis.2c00446
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Using genome mining and heterologous expression, we report the discovery and production of a new antimicrobial lasso peptide from species related to the Enterobacter cloacae complex. Using NMR and mass spectrometric analysis, we show that this lasso peptide, named cloacaenodin, employs a threaded lasso fold which imparts proteolytic resistance that its unthreaded counterpart lacks. Cloacaenodin has selective, low micromolar, antimicrobial activity against species related to the E. cloacae complex, including species implicated in nosocomial infections and against clinical isolates of carbapenem-resistant Enterobacterales. We further used site-directed mutagenesis to probe the importance of specific residues to the peptide's biosynthesis, stability, and bioactivity.
引用
收藏
页码:111 / 121
页数:11
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