AI-2 Biosynthesis Module in a Magnetic Nanofactory Alters Bacterial Response Via Localized Synthesis and Delivery

被引:24
作者
Fernandes, Rohan [1 ,2 ]
Bentley, William E. [1 ,2 ]
机构
[1] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
[2] Univ Maryland, Inst Biotechnol, Ctr Biosyst Res, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
nanofactory; magnetic nanofactories; synthesis module and cell capture module; AI-2; quorum sensing; localized synthesis and delivery; CHITOSAN-CONJUGATED MAGNETITE; QUORUM-SENSING SIGNAL; ESCHERICHIA-COLI; VIBRIO-HARVEYI; S-RIBOSYLHOMOCYSTEINASE; MOLECULE AUTOINDUCER-2; STREPTOCOCCUS-MUTANS; PATHOGENIC BACTERIA; CATALYTIC MECHANISM; BIOFILM FORMATION;
D O I
10.1002/bit.22078
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nanofactories are nano-dimensioned and comprised of modules serving various functions that alter the response of targeted cells when deployed by locally synthesizing and delivering cargo to the surfaces of the targeted cells. In its basic form, a nanofactory consists of a minimum of two functional modules: a cell capture module and a synthesis module. In this work, magnetic nanofactories that alter the response of targeted bacteria by the localized synthesis and delivery of the "universal" bacterial quorum sensing signal molecule autoinducer AI-2 are demonstrated. The magnetic nanofactories consist of a cell capture module (chitosan-mag nanoparticles) and an AI-2 biosynthesis module that contains both AI-2 biosynthetic enzymes Pfs and LLIXS on a fusion protein (His-LuxS-Pfs-Tyr, HLPT) assembled together. HUT is hypothesized to be more efficient than its constituent enzymes (used separately) at conversion of the substrate SAH to product AI-2 on account of the proximity of the two enzymes within the fusion protein. HLPT is demonstrated to be more active than the constituent enzymes, Pfs and LuxS, over a wide range of experimental conditions. The magnetic nanofactories (containing bound HLPT) are also demonstrated to be more active than free, unbound HLPT. They are also shown to elicit an increased response in targeted Escherichia coli cells, due to the localized synthesis and delivery of AI-2, when compared to the response produced by the addition of AI-2 directly to the cells. Studies investigating the univvrsality of AI-2 and unraveling AI-2 based quorum sensing in bacteria using magnetic nanofactories are envisioned. The prospects of using such multi-modular nanofactories in developing the next generation of antimicrobials based on intercepting and interrupting quorum sensing based signaling are discussed.
引用
收藏
页码:390 / 399
页数:10
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