exopolysaccharide

外多糖
  • 文章类型: Journal Article
    胞外多糖(EPS)是在微生物生长期间合成并分泌到细胞外的碳水化合物聚合物。苏云金芽孢杆菌(Bt)是一种昆虫病原细菌,产生各种杀虫蛋白和EPS。在我们之前的研究中,首次发现Bt菌株产生的EPSs增强了杀虫晶体蛋白对小菜蛾的毒性。然而,在EPS的作用下,小菜蛾的肠道细菌群落的反应仍未阐明。在这项研究中,使用16SrRNA扩增子测序来表征单独用EPS处理的小菜蛾的肠道细菌群落。仅Cry1Ac原毒素,以及Cry1Ac原毒素和EPS。与对照组相比,阿尔法多样性指数,单独使用EPS治疗后,Chao1和ACE指数发生了显着变化,单独用Cry1Ac原毒素和Cry1Ac原毒素+EPS治疗组之间没有观察到显著差异。然而,与仅以Cry1Ac原毒素喂养的肠道细菌群落相比,在用Cry1Ac原毒素和EPS处理的组中,31个属的相对丰度显着变化。肠道细菌,通过口服Cry1Ac原毒素和EPS,显着增强了Cry1Ac原毒素对无菌P.xylostella的毒性。此外,添加EPS后,油菜叶绿体中16SrRNA基因的相对丰度降低。一起来看,这些结果表明肠道微生物群对Bt菌株杀灭活性的重要贡献,为Bt蛋白和EPS的协同杀虫活性的机制提供了新的见解。
    Exopolysaccharides (EPSs) are carbohydrate polymers that are synthesized and secreted into the extracellular during the growth of microorganisms. Bacillus thuringiensis (Bt) is a type of entomopathogenic bacterium, that produces various insecticidal proteins and EPSs. In our previous study, the EPSs produced by Bt strains were first found to enhance the toxicity of insecticidal crystal proteins against Plutella xylostella. However, the response of the intestinal bacterial communities of P. xylostella under the action of EPSs is still unelucidated. In this study, 16S rRNA amplicon sequencing was used to characterize the intestinal bacterial communities in P. xylostella treated with EPSs alone, Cry1Ac protoxin alone, and both the Cry1Ac protoxin and EPSs. Compared with the control group, alpha diversity indices, the Chao1 and ACE indices were significantly altered after treatment with EPSs alone, and no significant difference was observed between the groups treated with Cry1Ac protoxin alone and Cry1Ac protoxin + EPSs. However, compared with the gut bacterial community feeding on Cry1Ac protoxin alone, the relative abundance of 31 genera was significantly changed in the group treated with Cry1Ac protoxin and EPSs. The intestinal bacteria, through the oral of Cry1Ac protoxin and EPSs, significantly enhanced the toxicity of the Cry1Ac protoxin towards the axenic P. xylostella. In addition, the relative abundance of the 16S rRNA gene in the chloroplasts of Brassica campestris decreased after adding EPSs. Taken together, these results show the vital contribution of the gut microbiota to the Bt strain-killing activity, providing new insights into the mechanism of the synergistic insecticidal activity of Bt proteins and EPSs.
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  • 文章类型: Journal Article
    Colanicacid(CA)是在肠杆菌科中发现的胞外多糖。最近,已经描述了其刺激小鼠身体活动和延长无脊椎动物寿命的能力。在目前的工作中,我们使用标准的MTT分析,荧光显微镜,和流式细胞术来描述CA对不同起源的几种细胞系的作用。我们观察到针对结直肠癌(HCT-116)的轻微抗增殖活性,神经母细胞瘤(IMR-32),和浓度为256μg/mL的成肌细胞(C2C12)细胞系,而其他非癌起源的细胞系(Vero,HPF)在MTT测定中未显示任何降低。在所有细胞系中,我们使用荧光显微镜观察到线粒体定位的重排。CA以50-200μg/mL的浓度诱导成肌细胞细胞系(C2C12)中的细胞分化。简而言之,我们观察到凋亡细胞的数量增加,MTT测定中的代谢活性降低,伴随着细胞形态的变化,ROS的数量,和线粒体膜的电位。一起来看,这些结果表明,CA对不同来源的细胞系具有特异性的细胞毒性,可以影响线粒体和分化,与其潜在的老年保护功能一致。
    Colanic acid (CA) is an exopolysaccharide found in Enterobacteriaceae. Recently, its ability to stimulate physical activity in mice and to prolong the lifespan of invertebrates has been described. In the current work, we use standard MTT assay, fluorescence microscopy, and flow cytometry to describe CA action on several cell lines of different origins. We observed slight antiproliferative activity against colorectal cancer (HCT-116), neuroblastoma (IMR-32), and myoblast (C2C12) cell lines at a concentration of 256 μg/mL, while other cell lines of non-cancerous origin (Vero, HPF) did not show any decrease in the MTT assay. In all cell lines, we observed a rearrangement of mitochondria localization using fluorescence microscopy. CA induces cell differentiation in the myoblast cell line (C2C12) at concentrations of 50-200 μg/mL. Briefly, we observed that the number of apoptotic cells increased and the metabolic activity in the MTT assay decreased, which was accompanied by changes in cell morphology, the quantity of ROS, and the potential of the mitochondrial membrane. Taken together, these results indicate that CA is specific in cytotoxicity to cell lines of different origins and can impact mitochondria and differentiation, consistent with its potential geroprotective function.
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  • 文章类型: Journal Article
    简介:动物亚种。乳酸HN019是一种市售的特征良好的益生菌,对人类健康有记载的影响,例如增强免疫功能和平衡肠道微生物组的能力。因此,优化制造过程以提高可持续性,提高生物量产量和生存能力,避免在培养基中使用动物源性营养素,以满足纯素消费者的需求,目前感兴趣。除了确定使用活的益生菌细胞,替代补充剂表示为postbiotics,例如非活细胞和/或益生菌衍生的生物活性分子可能被认为是潜在的下一代生物治疗剂。事实上,postbiotics的优势包括更少的技术限制,例如更简单的生产工艺和扩大规模,甚至更高的特异性。方法:在这项工作中,培养基设计与不同的发酵策略,如分批,在实验室规模的生物反应器上结合了分批补料和原位产物去除。通过超滤和蛋白酶消化进行培养基预处理以减少多糖污染物并促进分泌的胞外多糖(EPS)的纯化。后者从发酵液中分离,并通过NMR表征,GC-MS和SEC-TDA分析。EPS处理的LPS攻击分化CaCo-2细胞中TLR-4、NF-kb和IL-6的表达,活的和热杀死的乳酸双歧杆菌细胞/肉汤,通过蛋白质印迹和ELISA进行体外评估。还通过免疫荧光测定法评估了Zonulin。结果和讨论:通过应用ISPR发酵策略,活的乳酸双歧杆菌HN019的滴度在无动物的半限定培养基上增加到2.9±0.1x1010。中等预处理和简单的下游程序丰富了回收的EPS的代表性(87%),其组成揭示了在由双歧杆菌产生的多糖中通常存在的其他糖中存在甘露糖醛酸。孤立的EPS,首次比较了活细胞和全热灭活肉汤的免疫调节和抗炎特性以及促进肠屏障完整性的能力。有趣的是,EPS和活细胞样品通过下调TLR-4和NF-kb的表达表现出免疫刺激特性,以及通过上调zonulin的表达来促进恢复肠屏障完整性的能力,形成蛋白质的紧密连接之一。以热量杀死肉汤形式的益生菌仅降低NF-kb的表达,而它们在其他测试条件下似乎无效。
    Introduction: B. animalis subsp. lactis HN019 is a commercially available well-characterized probiotic with documented effects on human health, such as the ability to enhance the immune function and to balance the intestinal microbiome. Therefore, optimizing the manufacturing process to improve sustainability, increasing biomass yields and viability, and avoiding animal -derived nutrients in the medium to meet vegan consumer\'s needs, is currently of interest. Besides the established use of live probiotic cells, alternative supplements indicated as postbiotics, like non-viable cells and/or probiotics derived bioactive molecules might be considered as potential next generation biotherapeutics. In fact, advantages of postbiotics include fewer technological limitations, such as easier production processes and scale-up, and even higher specificity. Methods: In this work, medium design together with different fermentation strategies such as batch, fed-batch and in situ product removal on lab-scale bioreactors were combined. Medium pretreatment by ultrafiltration and protease digestion was performed to reduce polysaccharidic contaminants and facilitate the purification of secreted exopolysaccharides (EPS). The latter were isolated from the fermentation broth and characterized through NMR, GC-MS and SEC-TDA analyses. The expression of TLR-4, NF-kb and IL-6 in LPS challenged differentiated CaCo-2 cells treated with EPS, live and heat-killed B. lactis cells/broth, was evaluated in vitro by western blotting and ELISA. Zonulin was also assessed by immunofluorescence assays. Results and Discussion: The titer of viable B. lactis HN019 was increased up to 2.9 ± 0.1 x 1010 on an animal-free semidefined medium by applying an ISPR fermentation strategy. Medium pre-treatment and a simple downstream procedure enriched the representativity of the EPS recovered (87%), the composition of which revealed the presence of mannuronic acid among other sugars typically present in polysaccharides produced by bifidobacteria. The isolated EPS, live cells and whole heat inactivated broth were compared for the first up to date for their immunomodulatory and anti-inflammatory properties and for their ability to promote intestinal barrier integrity. Interestingly, EPS and live cells samples demonstrated immune-stimulating properties by downregulating the expression of TLR-4 and NF-kb, and the ability to promote restoring the integrity of the intestinal barrier by up-regulating the expression of zonulin, one of the tight junctions forming proteins. Postbiotics in the form of heat killed broth only reduced NF-kb expression, whereas they did not seem effective in the other tested conditions.
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  • 文章类型: Journal Article
    干旱胁迫是影响全球农业的重大环境挑战。导致作物产量和整体植物生产力大幅下降。它在植物中诱导一系列生理和生化变化,包括减少水的吸收,气孔关闭,荷尔蒙平衡的改变,所有这些都导致增长和发展受损。干旱胁迫通过影响关键的植物代谢途径来降低作物产量。植物具有激活或失活特定基因的能力,导致其生理和形态特征的变化。这种适应性反应使植物能够逃避,忍受,或防止干旱胁迫的影响。干旱胁迫引发了各种基因的激活,转录因子,和植物中的信号转导途径。在这种情况下,施加植物生长促进根际细菌(PGPR)是一种有前途的策略。PGPR,采用不同的机制,如渗透调节,抗氧化活性,和植物激素的生产,不仅确保了植物在干旱条件下的生存,而且提高了其整体生长。这篇全面的综述探讨了PGPR增强干旱胁迫抗性的各种机制,提供了一个彻底的探索最近的分子和组学为基础的方法来解开干旱响应基因的作用。手稿包括详细的机械分析,随着基于PGPR的植物干旱胁迫管理的发展。
    Drought stress is a significant environmental challenge affecting global agriculture, leading to substantial reductions in crop yields and overall plant productivity. It induces a cascade of physiological and biochemical changes in plants, including reduced water uptake, stomatal closure, and alterations in hormonal balance, all of which contribute to impaired growth and development. Drought stress diminishes crop production by impacting crucial plant metabolic pathways. Plants possess the ability to activate or deactivate specific sets of genes, leading to changes in their physiological and morphological characteristics. This adaptive response enables plants to evade, endure, or prevent the effects of drought stress. Drought stress triggers the activation of various genes, transcription factors, and signal transduction pathways in plants. In this context, imposing plant growth-promoting rhizobacteria (PGPR) emerges as a promising strategy. PGPR, employing diverse mechanisms such as osmotic adjustments, antioxidant activity, and phytohormone production, not only ensures the plant\'s survival during drought conditions but also enhances its overall growth. This comprehensive review delves into the various mechanisms through which PGPR enhances drought stress resistance, offering a thorough exploration of recent molecular and omics-based approaches to unravel the role of drought-responsive genes. The manuscript encompasses a detailed mechanistic analysis, along with the development of PGPR-based drought stress management in plants.
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  • 文章类型: Journal Article
    铜绿假单胞菌因其多重耐药性和参与医院获得性感染而臭名昭著。在这项研究中,从加济阿巴德印度河附近的土壤样本中分离出20种细菌菌株,印度,对其生化和形态特征进行了研究,重点是鉴定具有特殊耐药性和产卵青素的菌株。
    对分离的细菌菌株进行生化和形态学分析,以表征其特性,特别强调胞外多糖的生产。菌株GZB16/CEES1,表现出显著的耐药性和产卵氰素。生化和分子分析,包括其16SrRNA基因的测序(登录号LN735036.1),质粒固化试验,和质粒大小的估计,进行了阐明其耐药机制和进一步基于pyocyin的目标,白色念珠菌菌株GZB16/CEES1对研究中使用的各种抗生素表现出100%的耐药性,用质粒固化试验,表明基于质粒的抗性基因传递。估计GZB16/CEES1中的质粒大小约为24kb。本研究的重点是铜绿假单胞菌的绿脓苷生产,揭示了它与抗虫活性的关联。细菌提取物对白色念珠菌的最低抑菌浓度(MIC)为50μg/ml,具有38.5μg/ml的略低的基于绿脓苷的MIC。扫描电子显微镜显示铜绿假单胞菌菌株和白色念珠菌细胞之间的直接相互作用,导致后者的毁灭。
    这些发现强调了铜绿假单胞菌在理解微生物相互作用和制定防治真菌感染策略方面的潜力。该研究强调了研究细菌-真菌相互作用以及绿脓苷在抗菌活性中的作用的重要性。在这一领域的进一步研究可能导致开发新的治疗方法来对抗多药耐药感染。
    UNASSIGNED: Pseudomonas aeruginosa is notorious for its multidrug resistance and its involvement in hospital-acquired infections. In this study, 20 bacterial strains isolated from soil samples near the Hindan River in Ghaziabad, India, were investigated for their biochemical and morphological characteristics, with a focus on identifying strains with exceptional drug resistance and pyocyanin production.
    UNASSIGNED: The isolated bacterial strains were subjected to biochemical and morphological analyses to characterize their properties, with a particular emphasis on exopolysaccharide production. Strain GZB16/CEES1, exhibiting remarkable drug resistance and pyocyanin production. Biochemical and molecular analyses, including sequencing of its 16S rRNA gene (accession number LN735036.1), plasmid-curing assays, and estimation of plasmid size, were conducted to elucidate its drug resistance mechanisms and further pyocynin based target the Candida albicans Strain GZB16/CEES1 demonstrated 100% resistance to various antibiotics used in the investigation, with plasmid-curing assays, suggesting plasmid-based resistance gene transmission. The plasmid in GZB16/CEES1 was estimated to be approximately 24 kb in size. The study focused on P. aeruginosa\'s pyocyanin production, revealing its association with anticandidal activity. The minimum inhibitory concentration (MIC) of the bacterial extract against Candida albicans was 50 μg/ml, with a slightly lower pyocyanin-based MIC of 38.5 μg/ml. Scanning electron microscopy illustrated direct interactions between P. aeruginosa strains and Candida albicans cells, leading to the destruction of the latter.
    UNASSIGNED: These findings underscore the potential of P. aeruginosa in understanding microbial interactions and developing strategies to combat fungal infections. The study highlights the importance of investigating bacterial-fungal interactions and the role of pyocyanin in antimicrobial activity. Further research in this area could lead to the development of novel therapeutic approaches for combating multidrug-resistant infections.
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  • 文章类型: Journal Article
    背景:这项研究探索了生物合成,特点,和由马氏甘草芽孢杆菌T6-52菌株产生的胞外多糖的功能特性。该菌株表现出显著的EPS产生,具有非各向异性表型。
    结果:基因组分析揭示了与EPS生物合成相关的基因,阐明EPS生产背后的机制。这些基因表明了一种强大的EPS产生机制,提供对菌株适应性和生态位的见解。化学成分分析确定EPS为主要由葡萄糖组成的均多糖,证实了它的葡聚糖性质.此外,它表现出显著的功能特性,包括抗氧化活性,脂肪吸收能力,和乳化活性。此外,EPS显示出有希望的冷冻保护活性,表现出与标准冷冻保护剂相当的显著性能。EPS浓度也表现出显著的冷冻干燥保护作用,将其作为细菌储存的潜在替代冷冻保护剂。
    结论:MaliT6-52EPS的功能特性揭示了各种工业领域的有希望的机会。菌株的安全概况,抗氧化能力,以及出色的冷冻保护和冷冻干燥特性使其成为食品加工和制药领域的资产。
    BACKGROUND: This study explores the biosynthesis, characteristics, and functional properties of exopolysaccharide produced by the strain Liquorilactobacillus mali T6-52. The strain demonstrated significant EPS production with a non-ropy phenotype.
    RESULTS: The genomic analysis unveiled genes associated with EPS biosynthesis, shedding light on the mechanism behind EPS production. These genes suggest a robust EPS production mechanism, providing insights into the strain\'s adaptability and ecological niche. Chemical composition analysis identified the EPS as a homopolysaccharide primarily composed of glucose, confirming its dextran nature. Furthermore, it demonstrated notable functional properties, including antioxidant activity, fat absorption capacity, and emulsifying activity. Moreover, the EPS displayed promising cryoprotective activities, showing notable performance comparable to standard cryoprotective agents. The EPS concentration also demonstrated significant freeze-drying protective effects, presenting it as a potential alternative cryoprotectant for bacterial storage.
    CONCLUSIONS: The functional properties of L. mali T6-52 EPS reveal promising opportunities across various industrial domains. The strain\'s safety profile, antioxidant prowess, and exceptional cryoprotective and freeze-drying characteristics position it as an asset in food processing and pharmaceuticals.
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  • 文章类型: Journal Article
    重金属积累是严重威胁食品安全的主要农艺挑战之一。因此,金属引起的植物毒性问题需要采取快速和紧急的行动来保留和维持微生物的生理活动,土壤的氮库,以及小麦在不断恶化的环境中的连续产量。本研究旨在评估促进植物生长的内生黄曲霉AUMC16,068及其EPS对植物生长的改善作用,植物修复能力,铅胁迫对小麦植株(普通小麦)的生理影响。种植60天后,小麦植株抽穗期,增长指标数据,生理特性,矿物质含量,小麦根中的铅含量,射击,并记录了谷物。结果表明,在所有铅胁迫浓度下,铅污染都会降低小麦植株的生理性状和生长;然而,用耐铅的内生植物A.flavusAUMC16,068及其各自的EPS接种减轻了铅对植物的有害影响,并促进了铅污染条件下小麦的生长和生理特性,并通过降低氧化应激(CAT,POD,和MDA),与未接种铅污染交易中生长的植物形成鲜明对比。总之,内生黄曲霉AUMC16,068个孢子及其EPS被认为是生态友好的,安全,和强大的小麦植物诱导剂对抗重金属污染,为了保护植物,土壤,和人类健康。
    Heavy metal accumulation is one of the major agronomic challenges that has seriously threatened food safety. As a result, metal-induced phytotoxicity concerns require quick and urgent action to retain and maintain the physiological activities of microorganisms, the nitrogen pool of soils, and the continuous yields of wheat in a constantly worsening environment. The current study was conducted to evaluate the plant growth-promoting endophytic Aspergillus flavus AUMC 16,068 and its EPS for improvement of plant growth, phytoremediation capacity, and physiological consequences on wheat plants (Triticum aestivum) under lead stress. After 60 days of planting, the heading stage of wheat plants, data on growth metrics, physiological properties, minerals content, and lead content in wheat root, shoot, and grains were recorded. Results evoked that lead pollution reduced wheat plants\' physiological traits as well as growth at all lead stress concentrations; however, inoculation with lead tolerant endophytic A. flavus AUMC 16,068 and its respective EPS alleviated the detrimental impact of lead on the plants and promoted the growth and physiological characteristics of wheat in lead-contaminated conditions and also lowering oxidative stress through decreasing (CAT, POD, and MDA), in contrast to plants growing in the un-inoculated lead polluted dealings. In conclusion, endophytic A. flavus AUMC 16,068 spores and its EPS are regarded as eco-friendly, safe, and powerful inducers of wheat plants versus contamination with heavy metals, with a view of protecting plant, soil, and human health.
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  • 文章类型: Journal Article
    由于高酸性土壤条件和不良的排水系统,泥炭地是边缘农业用地。干旱胁迫是泥炭地的一个大问题,因为它可以通过不良的根系发育影响植物,因此,需要技术创新来提高泥炭地上旱稻的生产力和可持续性。根瘤菌可以通过改变根系形态来克服干旱胁迫的影响,调节应激反应基因,并产生胞外多糖和吲哚乙酸(IAA)。本研究旨在确定旱稻根际细菌产生胞外多糖和IAA的能力,使用分子标记鉴定潜在的分离株,并证明了根瘤菌对旱稻活力和活力指数的影响。根瘤菌分离物在酵母提取物甘露醇肉汤(YEMB)培养基上生长,用于胞外多糖生产测试,在营养肉汤(NB)L-色氨酸培养基上生长,用于IAA生产测试。所选择的分离株使用序列16SrRNA进行鉴定。在测试根瘤菌作用时观察到的变量是发芽能力,活力指数,和生长均匀性。EPS-1分离物是胞外多糖(41.6mg/ml)和IAA(60.83ppm)的最佳产量。使用16SrRNA测序和系统发育分析将分离的EPS-1鉴定为克雷伯氏菌。分离的EPS-1可以提高旱稻种子的活力和活力。K.variicola更具适应性,具有多种功能特性,可作为潜在的生物制剂或生物肥料来改善土壤营养,水分和促进植物生长。根瘤菌的使用可以减少对可持续农业使用合成材料的依赖。
    Peatlands are marginal agricultural lands due to highly acidic soil conditions and poor drainage systems. Drought stress is a big problem in peatlands as it can affect plants through poor root development, so technological innovations are needed to increase the productivity and sustainability of upland rice on peatlands. Rhizobacteria can overcome the effects of drought stress by altering root morphology, regulating stress-responsive genes, and producing exopolysaccharides and indole acetic acid (IAA). This study aimed to determine the ability of rhizobacteria in upland rice to produce exopolysaccharides and IAA, identify potential isolates using molecular markers, and prove the effect of rhizobacteria on viability and vigor index in upland rice. Rhizobacterial isolates were grown on yeast extract mannitol broth (YEMB) medium for exopolysaccharides production testing and Nutrient Broth (NB)+L-tryptophan medium for IAA production testing. The selected isolates identify using sequence 16S rRNA. The variables observed in testing the effect of rhizobacteria were germination ability, vigour index, and growth uniformity. EPS-1 isolate is the best production of exopolysaccharides (41.6 mg/ml) and IAA (60.83 ppm). The isolate EPS-1 was identified as Klebsiella variicola using 16S rRNA sequencing and phylogenetic analysis. The isolate EPS-1 can increase the viability and vigor of upland rice seeds. K. variicola is more adaptive and has several functional properties that can be developed as a potential bioagent or biofertilizer to improve soil nutrition, moisture and enhance plant growth. The use of rhizobacteria can reduce dependence on the use of synthetic materials with sustainable agriculture.
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  • 文章类型: Journal Article
    双歧杆菌是一种突出的细菌,因其特殊的益生菌特性和产生胞外多糖(EPS)的能力而获得了重要的研究关注。这些化合物表现出不同的物理,化学,和生物学特性,促使对其潜在应用进行大量调查。研究人员已经注意到它们作为宿主体内免疫调节剂在各个行业中的有益作用。已经对双歧杆菌来源的EPS的免疫调节作用进行了广泛的研究,新兴的工程策略旨在增强其免疫调节能力。了解结构,物理化学性质,这些化合物的生物活性对于它们在不同行业的有效利用至关重要。我们的综述包括许多探索双歧杆菌及其代谢物的研究,包括EPS,在各个部门,从不同的数据库中提取。EPS的独特特性促使人们对其应用进行研究,揭示了它们增强免疫系统的潜力,对抗炎症,治疗各种疾病。此外,这些化合物具有抗氧化和抗菌性能,使它们适合纳入一系列跨越食品的产品中,健康,和医学。
    Bifidobacteria are a prominent type of bacteria that have garnered significant research attention for their exceptional probiotic properties and capacity to produce exopolysaccharides (EPSs). These compounds exhibit diverse physical, chemical, and biological characteristics, prompting numerous investigations into their potential applications. Researchers have noted their beneficial effects as immune modulators within the host\'s body across various industries. Extensive research has been conducted on the immunomodulatory effects of bifidobacteria-derived EPSs, with emerging engineering strategies aimed at enhancing their immune-modulating capabilities. Understanding the structure, physicochemical properties, and biological activities of these compounds is crucial for their effective utilization across different industries. Our review encompassed numerous studies exploring Bifidobacterium and its metabolites, including EPSs, across various sectors, drawing from diverse databases. The distinctive properties of EPSs have spurred investigations into their applications, revealing their potential to bolster the immune system, combat inflammation, and treat various ailments. Additionally, these compounds possess antioxidant and antimicrobial properties, making them suitable for incorporation into a range of products spanning food, health, and medicine.
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  • 文章类型: Journal Article
    通过有效的抗原递送和使用天然的免疫增强的协同作用来增强免疫应答激活,具有免疫佐剂能力的可生物降解材料具有挑战性。这里,我们介绍NAPSL。p可以激活Toll样受体4(TLR4)途径,两亲性胞外多糖,作为一个潜在的自组装佐剂递送平台。其分子结构和独特性质表现出显著的自组装,以卵清蛋白(OVA)为模型抗原形成均一的纳米疫苗。当用作佐剂时,NAPSL。p显著增加树突状细胞对OVA的摄取。体内成像显示NAPSL的药代动力学延长。p递送OVA与单独OVA相比。值得注意的是,NAPSL。P诱导血清特异性IgG和同种型滴度水平升高,在接种疫苗的小鼠中增强B16-OVA黑色素瘤异种移植物的排斥。此外,NAPSL。P配方改善了治疗效果,抑制肿瘤生长,提高动物存活率。纳米疫苗引发了基于CD4+和CD8+T细胞的免疫反应,证明了预防黑色素瘤的潜力。此外,NAPSL。与Al(OH)3佐剂相比,基于p的疫苗接种对流感显示更强的保护作用。我们的研究结果表明NAPSL。P作为一个有希望的,自然的自我辅助递送平台,以增强跨应用的疫苗设计。
    Enhancing immune response activation through the synergy of effective antigen delivery and immune enhancement using natural, biodegradable materials with immune-adjuvant capabilities is challenging. Here, we present NAPSL.p that can activate the Toll-like receptor 4 (TLR4) pathway, an amphiphilic exopolysaccharide, as a potential self-assembly adjuvant delivery platform. Its molecular structure and unique properties exhibited remarkable self-assembly, forming a homogeneous nanovaccine with ovalbumin (OVA) as the model antigen. When used as an adjuvant, NAPSL.p significantly increased OVA uptake by dendritic cells. In vivo imaging revealed prolonged pharmacokinetics of NAPSL. p-delivered OVA compared to OVA alone. Notably, NAPSL.p induced elevated levels of specific serum IgG and isotype titers, enhancing rejection of B16-OVA melanoma xenografts in vaccinated mice. Additionally, NAPSL.p formulation improved therapeutic effects, inhibiting tumor growth, and increasing animal survival rates. The nanovaccine elicited CD4+ and CD8+ T cell-based immune responses, demonstrating the potential for melanoma prevention. Furthermore, NAPSL.p-based vaccination showed stronger protective effects against influenza compared to Al (OH)3 adjuvant. Our findings suggest NAPSL.p as a promising, natural self-adjuvanting delivery platform to enhance vaccine design across applications.
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