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粘质沙雷氏菌次级代谢产物灵菌红素通过产生活性氧损伤生物分子来抑制铜绿假单胞菌生物膜的形成。

Serratia Secondary Metabolite Prodigiosin Inhibits Pseudomonas aeruginosa Biofilm Development by Producing Reactive Oxygen Species that Damage Biological Molecules.

作者信息

Kimyon Önder, Das Theerthankar, Ibugo Amaye I, Kutty Samuel K, Ho Kitty K, Tebben Jan, Kumar Naresh, Manefield Mike

机构信息

School of Biotechnology and Biomolecular Sciences, The University of New South Wales Sydney, NSW, Australia.

School of Biotechnology and Biomolecular Sciences, The University of New South WalesSydney, NSW, Australia; Department of Infectious Diseases and Immunology, Sydney Medical School, The University of SydneySydney, NSW, Australia.

出版信息

Front Microbiol. 2016 Jun 27;7:972. doi: 10.3389/fmicb.2016.00972. eCollection 2016.

DOI:10.3389/fmicb.2016.00972
PMID:27446013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4922266/
Abstract

Prodigiosin is a heterocyclic bacterial secondary metabolite belonging to the class of tripyrrole compounds, synthesized by various types of bacteria including Serratia species. Prodigiosin has been the subject of intense research over the last decade for its ability to induce apoptosis in several cancer cell lines. Reports suggest that prodigiosin promotes oxidative damage to double-stranded DNA (dsDNA) in the presence of copper ions and consequently leads to inhibition of cell-cycle progression and cell death. However, prodigiosin has not been previously implicated in biofilm inhibition. In this study, the link between prodigiosin and biofilm inhibition through the production of redox active metabolites is presented. Our study showed that prodigiosin (500 μM) (extracted from Serratia marcescens culture) and a prodigiosin/copper(II) (100 μM each) complex have strong RNA and dsDNA cleaving properties while they have no pronounced effect on protein. Results support a role for oxidative damage to biomolecules by H2O2 and hydroxyl radical generation. Further, it was demonstrated that reactive oxygen species scavengers significantly reduced the DNA and RNA cleaving property of prodigiosin. P. aeruginosa cell surface hydrophobicity and biofilm integrity were significantly altered due to the cleavage of nucleic acids by prodigiosin or the prodigiosin/copper(II) complex. In addition, prodigiosin also facilitated the bactericidal activity. The ability of prodigiosinto cause nucleic acid degradation offers novel opportunities to interfere with extracellular DNA dependent bacterial biofilms.

摘要

灵菌红素是一种杂环细菌次级代谢产物,属于三吡咯化合物类别,由包括沙雷氏菌属在内的多种细菌合成。在过去十年中,灵菌红素因其能够诱导多种癌细胞系凋亡而成为深入研究的对象。报告表明,灵菌红素在铜离子存在的情况下会促进双链DNA(dsDNA)的氧化损伤,从而导致细胞周期进程的抑制和细胞死亡。然而,灵菌红素此前尚未被认为与生物膜抑制有关。在本研究中,展示了灵菌红素与通过产生氧化还原活性代谢产物实现生物膜抑制之间的联系。我们的研究表明,灵菌红素(500μM)(从粘质沙雷氏菌培养物中提取)和灵菌红素/铜(II)(各100μM)复合物具有很强的RNA和dsDNA切割特性,而对蛋白质没有明显影响。结果支持了H2O2和羟基自由基生成对生物分子造成氧化损伤的作用。此外,已证明活性氧清除剂显著降低了灵菌红素的DNA和RNA切割特性。由于灵菌红素或灵菌红素/铜(II)复合物对核酸的切割,铜绿假单胞菌的细胞表面疏水性和生物膜完整性发生了显著改变。此外,灵菌红素还促进了杀菌活性。灵菌红素导致核酸降解的能力为干扰细胞外DNA依赖性细菌生物膜提供了新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/d2dc1e1a7f02/fmicb-07-00972-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/11fc2ac41c7b/fmicb-07-00972-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/d9592cfdcefb/fmicb-07-00972-g0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/0c1319bdb2d3/fmicb-07-00972-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/6857d42e828b/fmicb-07-00972-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/20dcd994adba/fmicb-07-00972-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/97199a87809b/fmicb-07-00972-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/57b07e19a0d4/fmicb-07-00972-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/d2dc1e1a7f02/fmicb-07-00972-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/11fc2ac41c7b/fmicb-07-00972-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/d9592cfdcefb/fmicb-07-00972-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/0c687ca28c9d/fmicb-07-00972-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/0c1319bdb2d3/fmicb-07-00972-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/6857d42e828b/fmicb-07-00972-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/20dcd994adba/fmicb-07-00972-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/97199a87809b/fmicb-07-00972-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/57b07e19a0d4/fmicb-07-00972-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff21/4922266/d2dc1e1a7f02/fmicb-07-00972-g0009.jpg

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