antimicrobial

抗菌剂
  • 文章类型: Journal Article
    四种未描述的聚酮化合物,beshanzoneA(1)和B(2)以及beshanhexanolsA(3)和B(4),从与极度濒危的中国特有针叶树冷杉相关的两种内生真菌的水稻发酵中分离出三种已知的(5-7)。γ-丁内酯衍生物1、2和5分离自Phomopsissp。BSZ-AZ-2,一种有趣的菌株,这次引起了我们的注意。在对青霉菌BSZ-P-4-1的后续研究中获得了环己醇衍生物3、4、6和7。化合物1-4的化学结构包括绝对构型通过光谱法测定,Mo2(OAc)4诱导电子圆二色性(IECD),GIAONMR计算和DP4+概率分析。特别是,化合物2包含一个新的5/5双环系统,其可以通过水解随后进行Aldol反应从已知化合物5生物源衍生。评估所有分离株对一小组细菌和真菌病原体的抗微生物活性。化合物6和7对白色念珠菌表现出中等抑制活性,MIC值为16和32μg/mL,分别。
    Four undescribed polyketides, beshanzones A (1) and B (2) as well as beshanhexanols A (3) and B (4), along with three known ones (5-7) were isolated from the rice fermentation of two endophytic fungi associated with the critically endangered Chinese endemic conifer Abies beshanzuensis. γ-Butyrolactone derivatives 1, 2, and 5 were isolated from Phomopsis sp. BSZ-AZ-2, an interesting strain that drawn our attention this time. The cyclohexanol derivatives 3, 4, 6, and 7 were obtained during a follow-up investigation on Penicillium commune BSZ-P-4-1. The chemical structures including absolute configurations of compounds 1-4 were determined by spectroscopic methods, Mo2(OAc)4 induced electronic circular dichroism (IECD), GIAO NMR calculations and DP4+ probability analyses. In particular, compound 2 contains a novel 5/5 bicyclic ring system, which might be biogenetically derived from the known compound 5 through hydrolysis followed by an Aldol reaction. All isolates were evaluated for their antimicrobial activities against a small panel of bacterial and fungal pathogens. Compounds 6 and 7 showed moderate inhibitory activities against Candida albicans, with MIC values of 16 and 32 μg/mL, respectively.
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  • 文章类型: Journal Article
    全球微生物耐药性严重威胁人类健康,和多靶向化合物被认为有希望对抗微生物抗性。在这项工作中,使用三乙氧基甲烷和取代的苯胺作为起始材料,通过多步反应开发了一系列具有多靶向抗菌潜力的新型噻唑基喹诺酮类药物。其结构经1HNMR确证,13CNMR和HRMS光谱。抗菌评价显示,一些目标化合物能有效抑制微生物生长。尤其是,硫代酰氨基肼基氨基噻唑基喹诺酮8a对耐药金黄色葡萄球菌具有很强的抑制活性,MIC值为0.0047mM,比诺氟沙星活性高5倍。高活性化合物8a表现出可忽略的溶血,在体外和体内没有明显的毒性,耐药性低,以及快速杀菌作用,这表明其良好的可药用性。此外,化合物8a能够有效地破坏细菌膜的完整性,插入DNA并抑制拓扑异构酶IV的活性,提示多靶向作用机制。化合物8a可以与DNA-拓扑异构酶IV复合物形成氢键和疏水相互作用,表明氨基噻唑基部分的插入有利于提高抗菌效率。这些发现表明,作为化学治疗候选物的活性硫代氨基肼酰氨基噻唑基喹诺酮8a显示出解决耐药细菌感染的巨大潜力。
    The global microbial resistance is a serious threat to human health, and multitargeting compounds are considered to be promising to combat microbial resistance. In this work, a series of new thiazolylquinolones with multitargeting antimicrobial potential were developed through multi-step reactions using triethoxymethane and substituted anilines as start materials. Their structures were confirmed by 1H NMR, 13C NMR and HRMS spectra. Antimicrobial evaluation revealed that some of the target compounds could effectively inhibit microbial growth. Especially, carbothioamido hydrazonyl aminothiazolyl quinolone 8a showed strong inhibitory activity toward drug-resistant Staphylococcus aureus with MIC value of 0.0047 mM, which was 5-fold more active than that of norfloxacin. The highly active compound 8a exhibited negligible hemolysis, no significant toxicity in vitro and in vivo, low drug resistance, as well as rapidly bactericidal effects, which suggested its favorable druggability. Furthermore, compound 8a was able to effectively disrupt the integrity of the bacterial membrane, intercalate into DNA and inhibit the activity of topoisomerase IV, suggesting multitargeting mechanism of action. Compound 8a could form hydrogen bonds and hydrophobic interactions with DNA-topoisomerase IV complex, indicating the insertion of aminothiazolyl moiety was beneficial to improve antibacterial efficiency. These findings indicated that the active carbothioamido hydrazonyl aminothiazolyl quinolone 8a as a chemical therapeutic candidate demonstrated immense potential to tackle drug-resistant bacterial infections.
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  • 文章类型: Journal Article
    各种各样的微生物以粘附的表面生物膜的形式与金属腐蚀密切相关。生物膜允许局部腐蚀性环境的发展和维持和/或允许包括点蚀在内的直接腐蚀。口腔环境中许多遗传上不同的微生物的存在对常规牙科中使用的金属假体和植入物的表面的完整性和耐久性构成威胁。然而,口腔微生物与特定腐蚀机制之间的关联尚不清楚。了解口腔环境中微生物腐蚀的发生方式以及金属材料的相关风险具有实际意义。这些知识对于越来越关注释放的腐蚀产物的生物活性的研究人员和临床医生也很重要。因此,主要目标是全面回顾目前有关口腔微生物影响腐蚀(MIC)的文献,包括生物膜和口腔环境的特征,MIC机制,在口腔微生物和潜在缓解技术存在下的腐蚀行为。发现包括口服MIC主要归因于微生物代谢过程中分泌的侵袭性代谢物(代谢物介导的MIC)。然而,从热力学的角度来看,不能排除通过菌毛或电子转移化合物的细胞外电子转移机制(EET-MIC)。各种减少MIC的方法已被证明是有效的在短期内,但是在考虑临床应用之前,需要进行长期评估。目前,大多数体外研究未能模拟口腔内生理条件的复杂性,这些条件可能会降低或加剧腐蚀风险,这必须在未来的研究中解决。重要性声明:对有关生物医学金属材料的口腔MIC(微生物影响的腐蚀)的文献进行了彻底的分析,包括口腔环境的特点,MIC机制,在存在典型口腔微生物和潜在缓解方法(材料设计和表面设计)的情况下的腐蚀行为。目前缺乏对口腔MIC的机械理解,这不仅对腐蚀研究人员而且对牙医和临床医生都非常重要。本文从生物腐蚀的角度讨论了生物膜的意义,并总结了口腔微生物可能引起的MIC机制的几个方面。在这项工作中,口腔MIC不仅与材料研究密切相关,而且与牙科/临床研究领域密切相关。
    A wide variety of microorganisms have been closely linked to metal corrosion in the form of adherent surface biofilms. Biofilms allow the development and maintenance of locally corrosive environments and/or permit direct corrosion including pitting corrosion. The presence of numerous genetically distinct microorganisms in the oral environment poses a threat to the integrity and durability of the surface of metallic prostheses and implants used in routine dentistry. However, the association between oral microorganisms and specific corrosion mechanisms is not clear. It is of practical importance to understand how microbial corrosion occurs and the associated risks to metallic materials in the oral environment. This knowledge is also important for researchers and clinicians who are increasingly concerned about the biological activity of the released corrosion products. Accordingly, the main goal was to comprehensively review the current literature regarding oral microbiologically influenced corrosion (MIC) including characteristics of biofilms and of the oral environment, MIC mechanisms, corrosion behavior in the presence of oral microorganisms and potentially mitigating technologies. Findings included that oral MIC has been ascribed mostly to aggressive metabolites secreted during microbial metabolism (metabolite-mediated MIC). However, from a thermodynamic point of view, extracellular electron transfer mechanisms (EET-MIC) through pili or electron transfer compounds cannot be ruled out. Various MIC mitigating methods have been demonstrated to be effective in short term, but long term evaluations are necessary before clinical applications can be considered. Currently most in-vitro studies fail to simulate the complexity of intraoral physiological conditions which may either reduce or exacerbate corrosion risk, which must be addressed in future studies. STATEMENT OF SIGNIFICANCE: A thorough analysis on literature regarding oral MIC (microbiologically influenced corrosion) of biomedical metallic materials has been carried out, including characteristics of oral environment, MIC mechanisms, corrosion behaviors in the presence of typical oral microorganisms and potential mitigating methods (materials design and surface design). There is currently a lack of mechanistic understanding of oral MIC which is very important not only to corrosion researchers but also to dentists and clinicians. This paper discusses the significance of biofilms from a biocorrosion perspective and summarizes several aspects of MIC mechanisms which could be caused by oral microorganisms. Oral MIC has been closely associated with not only the materials research but also the dental/clinical research fields in this work.
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  • 文章类型: Journal Article
    牙髓感染是由复杂的根管系统中微生物群落定植的相互作用活动引起的。本研究旨在更新纳米材料的最新知识,它们的抗菌机制,以及它们在牙髓学中的应用。使用PubMed数据库对牙髓应用中使用的纳米材料的当前知识进行了详细的文献综述。具有小尺寸的抗菌纳米材料,大的比表面积,引入高化学活性作为灌溉剂,光敏剂输送系统,和药物,或修改密封剂。纳米材料在牙髓领域的应用可以提高抗菌效率,增加牙本质小管渗透,改善治疗结果。这项研究支持纳米材料作为治疗牙髓感染的有希望的策略的潜力。
    Endodontic infections arise from the interactive activities of microbial communities colonizing in the intricate root canal system. The present study aims to update the latest knowledge of nanomaterials, their antimicrobial mechanisms, and their applications in endodontics. A detailed literature review of the current knowledge of nanomaterials used in endodontic applications was performed using the PubMed database. Antimicrobial nanomaterials with a small size, large specific surface area, and high chemical activity are introduced to act as irrigants, photosensitizer delivery systems, and medicaments, or to modify sealers. The application of nanomaterials in the endodontic field could enhance antimicrobial efficiency, increase dentin tubule penetration, and improve treatment outcomes. This study supports the potential of nanomaterials as a promising strategy in treating endodontic infections.
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  • 文章类型: Journal Article
    具有抗菌和载药功能的复合海绵在医学组织工程领域的应用前景广阔。以Ca(NO3)2为溶剂制备木薯丝素蛋白(CSF)溶液,然后将其与壳聚糖(CS)组合以通过冷冻干燥产生海绵多孔材料。通过氢键成功制备了具有网状结构的CSF-CS复合海绵。扫描电子显微镜(SEM),采用傅里叶变换红外吸收(FTIR)和X射线衍射(XRD)研究了木薯丝素材料的外观和结构,特别检查不同质量百分比的CS对海绵结构的影响。分析了CSF-CS海绵的溶胀率和力学性能,以及它的抗菌性能。此外,通过将布洛芬作为模型药物加入这些装载的海绵中,它们作为有效药物递送系统的潜在功效得到证实.结果表明,CSF-CS海绵具有三维多孔结构,孔隙率超过70%,膨胀率超过400%,同时还表现出良好的耐压性。此外,它表现出优异的药物携带能力,对大肠杆菌具有显著的抑菌效果。总的来说,这些发现支持将CSF-CS复合海绵视为用于药物递送系统或伤口敷料的可行候选物.
    The application prospects of composite sponges with antibacterial and drug-carrying functions in the field of medical tissue engineering are extensive. A solution of cassava silk fibroin (CSF) was prepared with Ca(NO3)2 as a solvent, which was then combined with chitosan (CS) to create a sponge-porous material by freeze-drying. The CSF-CS composite sponge with a mesh structure was successfully fabricated through hydrogen bonding. Scanning electron microscopy (SEM), Fourier transform infrared absorption (FTIR) and X-ray diffraction (XRD) were employed to investigate the appearance and structure of the cassava silk\'s fibroin materials, specifically examining the impact of different mass percentages of CS on the sponge\'s structure. The swelling rate and mechanical properties of the CSF-CS sponge were analyzed, along with its antibacterial properties. Furthermore, by incorporating ibuprofen as a model drug into these loaded sponges, their potential efficacy as efficient drug delivery systems was demonstrated. The results indicate that the CSF-CS sponge possesses a three-dimensional porous structure with over 70% porosity and an expansion rate exceeding 400% while also exhibiting good resistance against pressure. Moreover, it exhibits excellent drug-carrying ability and exerts significant bacteriostatic effects on Escherichia coli. Overall, these findings support considering the CSF-CS composite sponge as a viable candidate for use in drug delivery systems or wound dressings.
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  • 文章类型: Journal Article
    海藻酸钠(SA)广泛应用于食品中,生物医学,和化学工业由于其生物相容性,生物降解性,和优异的成膜性能。本文介绍了一种简单的方法,用于制备均匀的海藻酸盐基包装材料,具有出色的水果保鲜性能。海藻酸盐通过逐渐释放由葡糖酸内酯(GDL)的持续水解引发的钙离子而均匀交联。肉桂醛(CA)乳液,由黄原胶稳定,不使用传统表面活性剂,紧密地结合到海藻酸盐薄膜中以增强其抗菌性,抗氧化剂,和紫外线屏蔽性能。藻酸盐基薄膜有效地阻挡了400-200nm范围内的紫外线,同时允许高达70%的可见光透射率。此外,它显示出增加的水接触角和降低的水蒸气渗透性。藻酸盐基膜也通过造纸工业中常用的涂布工艺用于制备涂布纸。藻酸盐基材料表现出优异的抗氧化性能和对大肠杆菌的抗菌活性,金黄色葡萄球菌和灰葡萄孢菌,在室温下成功将草莓的保质期延长至7天。这种低成本和简便的方法有可能通过将活性油紧密结合到广泛的生物大分子底物上来推动食品和生物医学领域的进步。
    Sodium alginate (SA) is widely used in the food, biomedical, and chemical industries due to its biocompatibility, biodegradability, and excellent film-forming properties. This article introduces a simple method for preparing uniform alginate-based packaging materials with exceptional properties for fruit preservation. The alginate was uniformly crosslinked by gradually releasing calcium ions triggered by the sustained hydrolysis of gluconolactone (GDL). A cinnamaldehyde (CA) emulsion, stabilized by xanthan without the use of traditional surfactants, was tightly incorporated into the alginate film to enhance its antimicrobial, antioxidant, and UV shielding properties. The alginate-based film effectively blocked ultraviolet rays in the range of 400-200 nm, while allowing for a visible light transmittance of up to 70 %. Additionally, it showed an increased water contact angle and decreased water vapor permeability. The alginate-based film was also employed in the preparation of coated paper through the commonly used coating process in the papermaking industry. The alginate-based material displayed excellent antioxidant properties and antimicrobial activity against Escherichia coli, Staphylococcus aureus and Botrytis cinerea, successfully extending the shelf life of strawberries to 7 days at room temperature. This low-cost and facile method has the potential to drive advancements in the food and biomedical fields by tightly incorporating active oil onto a wide range of biomacromolecule substrates.
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  • 文章类型: Journal Article
    N-氯-N-氟苯磺酰胺(CFBSA),是一种新型的氯化试剂,具有潜在的抗菌活性。在这项研究中,CFBSA被确认为针对不同革兰氏阴性菌的广泛抗菌和杀菌药物,革兰氏阳性菌和真菌,同时发现它对真核细胞的细胞毒性较低。此外,微生物形态学分析和氧化应激试验用于确定CFBSA的抗菌机制。根据结果,CFBSA可能在细胞膜上具有靶标,并通过破坏其细胞膜来杀死微生物。然后,CFBSA首先通过静电纺丝与PLCL/SF组合并应用于伤口敷料。通过SEM研究了负载CFBSA的纳米纤维毡的不同PLCL/SF的表征,水接触角,FTIR,细胞相容性和抗菌试验。负载CFBSA的PLCL/SF纳米纤维垫显示出优异的抗微生物活性。为了平衡生物相容性和抗菌效率,选择SP-2.5作为进一步应用负载CFBSA的PLCL/SF的理想负载浓度。总之,静电纺丝CFBSA负载的PLCL/SF纳米纤维垫具有广谱抗菌和杀菌活性以及良好的生物相容性,显示出巨大的伤口敷料潜力。
    N-chloro-N-fluorobenzenesulfonylamide (CFBSA), was a novel chlorinating reagent, which exhibits potential antibacterial activities. In this study, CFBSA was confirmed as a wide-broad antimicrobial and bactericidal drug against different gram-negative bacteria, gram-positive bacteria and fungi, while it was found to have low cytotoxicity for eukaryotic cells. In addition, microorganism morphology assay and oxidative stress test was used to determine the antimicrobial mechanisms of CFBSA. According to the results, CFBSA probably had a target on cell membrane and killed microorganism by disrupting its cell membrane. Then, CFBSA was first combined with PLCL/SF via electrospinning and applied in wound dressings. The characterization of different PLCL/SF of CFBSA-loaded nanofibrous mats was investigated by SEM, water contact angle, FTIR, cell compatibility and antimicrobial test. CFBSA-loaded PLCL/SF nanofibrous mats showed excellent antimicrobial activities. In order to balance of the biocompatibility and antibacterial efficiency, SP-2.5 was selected as the ideal loading concentration for further application of CFBSA-loaded PLCL/SF. In conclusion, the electrospun CFBSA-loaded PLCL/SF nanofibrous mat with its broad-spectrum antimicrobial and bactericidal activity and good biocompatibility showed enormous potential for wound dressing.
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  • 文章类型: Journal Article
    广泛的机会性病原体对全球健康构成严重威胁,特别是在易感人群中。不断升级的抗生素耐药性危机凸显了对新型抗菌剂和替代治疗方法的迫切需要。中药及其化合物在感染性疾病的治疗中有着深厚的根基。它具有多种活性成分和多目标特性,为发现和开发抗菌药物开辟了新的途径。
    这项研究的重点是通过肉汤微量稀释和琼脂圆盘扩散方法评估神生-皮文变味药粉(SPC)提取物对机会性病原体感染的功效。此外,进行生物膜抑制和根除试验以评估SPC提取物的抗生物膜作用。
    用LC-MS分析代谢物分布。此外,通过细菌生长曲线分析研究了SPC和金属有机框架(MOF)之间的潜在协同作用。结果表明,SPC提取物对金黄色葡萄球菌具有抗菌活性,最低抑制浓度(MIC)为7.8mg/mL(原料药浓度)。值得注意的是,在1/2MIC,SPC提取物显著抑制生物膜形成,抑制超过80%,这对于解决慢性和医院获得性感染至关重要。金黄色葡萄球菌的代谢组学分析显示,SPC提取物诱导各种代谢物水平显着降低,包括L-脯氨酸,L-天冬酰胺.这表明SPC提取物可能干扰金黄色葡萄球菌的代谢。同时,生长曲线实验证明SPC提取物与MOFs具有协同抗菌作用。
    总而言之,本研究强调了SPC提取物作为抗金黄色葡萄球菌感染的新型抗菌剂的潜力,具有良好的生物膜抑制性能。在SPC提取物和MOFs之间观察到的协同作用进一步支持了该组合作为替代治疗方法的探索。
    UNASSIGNED: Widespread opportunistic pathogens pose a serious threat to global health, particularly in susceptible hospital populations. The escalating crisis of antibiotic resistance highlights the urgent need for novel antibacterial agents and alternative treatment approaches. Traditional Chinese Medicine (TCM) and its compounds have deep roots in the treatment of infectious diseases. It has a variety of active ingredients and multi-target properties, opening up new avenues for the discovery and development of antimicrobial drugs.
    UNASSIGNED: This study focuses on assessing the efficacy of the Shensheng-Piwen changed medicinal powder (SPC) extracts against opportunistic pathogen infections by broth microdilution and agar disc diffusion methods. Additionally, biofilm inhibition and eradication assays were performed to evaluate the antibiofilm effects of SPC extracts.
    UNASSIGNED: Metabolite profiles were analyzed by LC-MS. Furthermore, the potential synergistic effect between SPC and Metal-Organic Framework (MOF) was investigated by bacterial growth curve analysis. The results indicated that the SPC extracts exhibited antibacterial activity against S. aureus, with a minimum inhibitory concentration (MIC) of 7.8 mg/mL (crude drug concentration). Notably, at 1/2 MIC, the SPC extracts significantly inhibited biofilm formation, with over 80% inhibition, which was critical in tackling chronic and hospital-acquired infections. Metabolomic analysis of S. aureus revealed that SPC extracts induced a notable reduction in the levels of various metabolites, including L-proline, L-asparagine. This suggested that the SPC extracts could interfere with the metabolism of S. aureus. Meanwhile, the growth curve experiment proved that SPC extracts and MOFs had a synergistic antibacterial effect.
    UNASSIGNED: In conclusion, the present study highlights the potential of SPC extracts as a novel antibacterial agent against S. aureus infections, with promising biofilm inhibition properties. The observed synergistic effect between SPC extracts and MOFs further supports the exploration of this combination as an alternative treatment approach.
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  • 文章类型: Journal Article
    精油,以其抗真菌特性而闻名,被广泛用于对抗水果腐烂。然而,由于它们的高挥发性和疏水特性,它们的应用面临着巨大的挑战,导致强烈的气味,有效时间短,分散性差。本研究旨在通过配制由精油和鼠李糖脂组成的微乳液来解决这些挑战。优化的微乳液,具有6.8nm的小粒径,比常规乳液具有更高的稳定性和更低的挥发性。值得注意的是,所制备的微乳液对大肠杆菌表现出显著的抗菌效果,金黄色葡萄球菌,C.白色念珠菌,酿酒酵母,还有A.Niger.这些微乳液的应用被证明是非常有效的防止蓝莓腐烂,同时保持水果的质量,特别是通过减少必需营养素如花青素的损失。因此,精油微乳液是一种高效的水果采后防腐剂,提供了一个有前途的解决方案,以延长其保质期和提高整体质量。
    Essential oils, well-known for their antifungal properties, are widely utilized to combat fruit decay. However, their application faces big challenges due to their high volatility and hydrophobic traits, which leads to strong odor, short effective time and poor dispersivity. This study aimed to address these challenges by formulating microemulsions consisting of essential oils and rhamnolipids. The optimized microemulsion, featuring a small particle size of 6.8 nm, exhibited higher stability and lower volatility than conventional emulsion. Notably, the prepared microemulsions demonstrated remarkable antimicrobial efficacy against E. coli, S. aureus, C. albicans, S. cerevisiae, and A. niger. The application of these microemulsions proved to be highly effective in preventing blueberry decay while preserving fruit\'s quality, particularly by minimizing the loss of essential nutrients such as anthocyanins. Consequently, essential oil microemulsions emerge as a highly effective postharvest preservative for fruits, offering a promising solution to extend their shelf life and enhance overall quality.
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  • 文章类型: Journal Article
    耐甲氧西林金黄色葡萄球菌(MRSA)很容易在食品表面形成生物膜,从而导致交叉污染,这是难以删除的。因此,迫切需要找到具有良好抗菌和抗生物膜效果的替代品。在这项研究中,两种吲哚倍半萜化合物,Xiamycin(1)和氯化代谢产物氯霉素(2),从海洋链霉菌属的发酵液中分离出来。NBU3429第一次通过光谱数据解释对这两种化合物的化学结构进行了表征,包括1DNMR和HRESIMS分析。抑菌试验表明,氯霉素(2)(最低抑菌浓度,MIC=16μg/mL)对MRSAATCC43300的抗菌活性优于西霉素(1)(MIC=32μg/mL)。此外,化合物(2)在32-512μg/mL的浓度范围内,使MRSAATCC43300的生物膜形成率降低了12.7%-84.6%,也比Xiamycin(1)(4.1%-49.9%)相对更强。抗菌/抗生物膜机制研究表明,氯霉素(2)可以破坏MRSA的细胞壁和细胞膜,抑制生物膜胞外多糖的产生。所有这些结果表明,氯霉素(2)是一种有效的抗菌/抗生物膜剂,这使得它成为食品防腐剂的有吸引力的候选者。
    Methicillin-resistant Staphylococcus aureus (MRSA) can easily form biofilms on food surfaces, thus leading to cross-contamination, which is difficult to remove. Therefore, there is an urgent need to find alternatives with good antibacterial and antibiofilm effects. In this study, two indole sesquiterpene compounds, xiamycin (1) and chlorinated metabolite chloroxiamycin (2), were isolated from the fermentation liquid of marine Streptomyces sp. NBU3429 for the first time. The chemical structures of the two compounds were characterized by spectroscopic data interpretation, including 1D NMR and HRESIMS analysis. Antimicrobial test showed that chloroxiamycin (2) (minimum inhibitory concentration, MIC = 16 μg/mL) exhibited superior antibacterial activity than xiamycin (1) (MIC = 32 μg/mL) against MRSA ATCC43300. Moreover, compound (2) decreased the biofilm formation rate of MRSA ATCC43300 by 12.7%-84.6% in the concentration range of 32-512 μg/mL, which is relatively stronger than xiamycin (1) (4.1%-49.9%) as well. Antibacterial/antibiofilm mechanism investigation indicated that chloroxiamycin (2) could disrupt the cell wall and membrane of MRSA, inhibiting the production of biofilm extracellular polysaccharides. All these results illustrated that chloroxiamycin (2) is an effective antibacterial/antibiofilm agent, which makes it an attractive candidate for food preservatives.
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