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一种用于减少钢生物腐蚀的酶促群体淬灭涂层添加剂的现场测试。

Field testing of an enzymatic quorum quencher coating additive to reduce biocorrosion of steel.

作者信息

Huang Siqian, Bergonzi Celine, Smith Sherry, Hicks Randall E, Elias Mikael H

机构信息

Department of Biology, University of Minnesota Duluth , Duluth, Minnesota, USA.

Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota Biotechnology Institute , St. Paul, Minnesota, USA.

出版信息

Microbiol Spectr. 2023 Sep 5;11(5):e0517822. doi: 10.1128/spectrum.05178-22.

Abstract

Microbial colonization can be detrimental to the integrity of metal surfaces and lead to microbiologically influenced corrosion. Biocorrosion is a serious problem for aquatic and marine industries in the world and severely affects the maritime transportation industry by destroying port infrastructure and increasing fuel usage and the time and cost required for maintenance of transport vessels. Here, we evaluate the potential of a stable quorum quenching lactonase enzyme to reduce biocorrosion in the field. Over the course of 21 months, steel samples coated with lactonase-containing acrylic paint were submerged at two different sites and depths in the Duluth-Superior Harbor (Lake Superior, MN, USA) and benchmarked against controls, including the biological biocide surfactin. In this experiment, the lactonase treatment outperformed the surfactin biocide treatment and significantly reduced the number of corrosion tubercles (37%; < 0.01) and the corroded surface area (39%; < 0.01) as compared to the acrylic-coated control coupons. In an attempt to evaluate the effects of signal disruption of surface microbial communities and the reasons for lower corrosion levels, 16S rRNA sequencing was performed and community populations were analyzed. Interestingly, surface communities were similar between all treatments, and only minor changes could be observed. Among these changes, several groups, including sulfate-reducing bacteria (SRB), appeared to correlate with corrosion levels, and more specifically, SRB abundance levels were lower on lactonase-treated steel coupons. We surmise that these minute community changes may have large impacts on corrosion rates. Overall, these results highlight the potential use of stable quorum quenching lactonases as an eco-friendly antifouling coating additive. IMPORTANCE Biocorrosion severely affects the maritime transportation industry by destroying port infrastructure and increasing fuel usage and the time and cost required to maintain transport vessels. Current solutions are partly satisfactory, and the antifouling coating still largely depends on biocide-containing products that are harmful to the environment. The importance of microbial signaling in biofouling and biocorrosion is not elucidated. We here take advantage of a highly stable lactonase that can interfere with N-acyl homoserine lactone-based quorum sensing and remain active in a coating base. The observed results show that an enzyme-containing coating can reduce biocorrosion over 21 months in the field. It also reveals subtle changes in the abundance of surface microbes, including sulfate-reducing bacteria. This work may contribute to pave the way for strategies pertaining to surface microbiome changes to reduce biocorrosion.

摘要

微生物定殖会损害金属表面的完整性,并导致微生物影响的腐蚀。生物腐蚀是全球水产和海洋工业面临的一个严重问题,它通过破坏港口基础设施、增加燃料消耗以及运输船只维护所需的时间和成本,严重影响海运业。在此,我们评估了一种稳定的群体淬灭内酯酶在实际应用中减少生物腐蚀的潜力。在21个月的时间里,将涂有含内酯酶丙烯酸漆的钢样本浸没在美国明尼苏达州苏必利尔湖德卢斯-苏必利尔港的两个不同地点和深度,并与包括生物杀微生物剂表面活性素在内的对照样本进行对比。在本实验中,与涂有丙烯酸漆的对照样本相比,内酯酶处理的效果优于表面活性素杀微生物剂处理,显著减少了腐蚀瘤的数量(37%;P<0.01)和腐蚀表面积(39%;P<0.01)。为了评估表面微生物群落信号干扰的影响以及腐蚀水平降低的原因,我们进行了16S rRNA测序并分析了群落组成。有趣的是,所有处理组的表面群落相似,仅观察到微小变化。在这些变化中,包括硫酸盐还原菌(SRB)在内的几个菌群似乎与腐蚀水平相关,更具体地说,在经内酯酶处理的钢样本上,SRB的丰度水平较低。我们推测这些微小的群落变化可能对腐蚀速率有很大影响。总体而言,这些结果凸显了稳定的群体淬灭内酯酶作为一种环保型防污涂层添加剂的潜在用途。重要性生物腐蚀通过破坏港口基础设施、增加燃料消耗以及运输船只维护所需的时间和成本,严重影响海运业。目前的解决方案部分令人满意,防污涂层在很大程度上仍依赖于对环境有害的含杀微生物剂产品。微生物信号在生物污损和生物腐蚀中的重要性尚未阐明。我们在此利用一种高度稳定的内酯酶,它可以干扰基于N-酰基高丝氨酸内酯的群体感应,并在涂层基质中保持活性。观察结果表明,含酶涂层在实际应用中可在21个月内减少生物腐蚀。它还揭示了包括硫酸盐还原菌在内的表面微生物丰度的细微变化。这项工作可能有助于为通过改变表面微生物群落来减少生物腐蚀的策略铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d140/10580884/f931bedadb26/spectrum.05178-22.f001.jpg

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