The activity of hydrolytic enzymes and antibiotics against biofilms of bacteria isolated from industrial-scale cooling towers.

IF 4.3 2区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Microbial Cell Factories Pub Date : 2024-10-16 DOI:10.1186/s12934-024-02502-1
Marcus Vinícius Dias-Souza, Andrea Lima Alves, Sérgio Pagnin, Andrea Azevedo Veiga, Ihtisham Ul Haq, Wadi B Alonazi, Vera Lúcia Dos Santos
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Abstract

Background: Cooling towers (CTs) are crucial to myriad industrial processes, supporting thermal exchange between fluids in heat exchangers using water from lakes and rivers as coolant. However, CT water can sometimes introduce microbial contaminants that adhere to and colonize various surfaces within the CT system. These microorganisms can form biofilms, significantly hindering the system's thermal exchange efficiency. Current treatment strategies employ oxidizing biocides to prevent microbial growth. However, despite their affordability, they do not eliminate biofilms effectively and can lead to corrosive damage within the system. Herein, we aim to devise an anti-biofilm strategy utilizing hydrolytic enzymes (such as α-amylase, glucoamylase, pectin-lyase, cellulase, protease, and DNase) alongside antibiotics (including meropenem, ciprofloxacin, gentamicin, erythromycin, chloramphenicol, and ceftriaxone) to combat microbial growth and biofilm formation in cooling systems.

Results: All enzymes reduced the development of the biofilms significantly compared to controls (p < 0.05). The polysaccharidases exhibited biomass reduction of 90%, except for pectin-lyase (80%), followed by DNAse and protease at 43% and 49%, respectively. The antibiotics reduced the biofilms of 70% of isolates in concentration of > 2 mg/mL. The minimal biofilm eradication concentration (MBEC) lower than 1 mg/mL was detected for some 7-day-old sessile isolates. The enzymes and antibiotics were also used in combination against biofilms using the modified Chequerboard method. We found six synergistic combinations, with Fractional inhibitory concentrations (FIC) < 0.5, out of the ten tested. In the presence of the enzymatic mixture, MBECs presented a significant decrease (p < 0.05), at least 4-fold for antibiotics and 32-fold for enzymes. Moreover, we characterized high molecular weight (> 12 kDa) exopolysaccharides (EPS) from biofilms of ten isolates, and glycosyl composition analysis indicated a high frequency of glucose, mannose, erythrose, arabinose, and idose across isolates EPS contrasting with rhamnose, allose, and those carbohydrates, which were detected in only one isolate.

Conclusion: The synergistic approach of combining enzymes with antibiotics emerges as a highly effective and innovative strategy for anti-biofilm intervention, highlighting its potential to enhance biofilm management practices.

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水解酶和抗生素对从工业规模冷却塔中分离出来的细菌生物膜的活性。
背景:冷却塔(CT)对众多工业流程至关重要,它支持热交换器中流体之间的热交换,使用湖泊和河流中的水作为冷却剂。然而,CT 水有时会引入微生物污染物,这些污染物会附着在 CT 系统的各种表面并形成菌落。这些微生物会形成生物膜,严重影响系统的热交换效率。目前的处理策略采用氧化型杀菌剂来防止微生物生长。然而,尽管它们价格低廉,却不能有效消除生物膜,还可能导致系统内的腐蚀性损坏。在此,我们旨在设计一种抗生物膜策略,利用水解酶(如α-淀粉酶、葡糖淀粉酶、果胶裂解酶、纤维素酶、蛋白酶和 DNase)和抗生素(包括美罗培南、环丙沙星、庆大霉素、红霉素、氯霉素和头孢曲松)来对抗冷却系统中的微生物生长和生物膜形成:与对照组相比,所有酶都能显著减少生物膜的形成(p 2 毫克/毫升)。在一些 7 天的无柄分离物中检测到的最小生物膜根除浓度(MBEC)低于 1 毫克/毫升。我们还采用改良的棋盘法,将酶和抗生素结合使用来对付生物膜。糖基组成分析表明,在所有分离物的 EPS 中,葡萄糖、甘露糖、赤藓糖、阿拉伯糖和惰糖的频率较高,而鼠李糖、阿洛糖和这些碳水化合物仅在一种分离物中检测到:结合酶与抗生素的协同方法是一种高效、创新的抗生物膜干预策略,凸显了其加强生物膜管理实践的潜力。
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来源期刊
Microbial Cell Factories
Microbial Cell Factories 工程技术-生物工程与应用微生物
CiteScore
9.30
自引率
4.70%
发文量
235
审稿时长
2.3 months
期刊介绍: Microbial Cell Factories is an open access peer-reviewed journal that covers any topic related to the development, use and investigation of microbial cells as producers of recombinant proteins and natural products, or as catalyzers of biological transformations of industrial interest. Microbial Cell Factories is the world leading, primary research journal fully focusing on Applied Microbiology. The journal is divided into the following editorial sections: -Metabolic engineering -Synthetic biology -Whole-cell biocatalysis -Microbial regulations -Recombinant protein production/bioprocessing -Production of natural compounds -Systems biology of cell factories -Microbial production processes -Cell-free systems
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