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来自沙特阿拉伯分离的海洋酸性生物活性胞外多糖的抗葡萄球菌、抗肿瘤、免疫学及结构特征的体外评估

In Vitro Assessment of Antistaphylococci, Antitumor, Immunological and Structural Characterization of Acidic Bioactive Exopolysaccharides from Marine   Isolated from Saudi Arabia.

作者信息

Selim Samy, Almuhayawi Mohammed S, Alharbi Mohanned Talal, Nagshabandi Mohammed K, Alanazi Awadh, Warrad Mona, Hagagy Nashwa, Ghareeb Ahmed, Ali Abdallah S

机构信息

Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Jouf University, Sakaka 72341, Saudi Arabia.

Department of Medical Microbiology and Parasitology, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia.

出版信息

Metabolites. 2022 Feb 1;12(2):132. doi: 10.3390/metabo12020132.

Abstract

A strain of was isolated from the Saudi Red Sea coast and identified based on culture features, biochemical characteristics, and phylogenetic analysis of 16S rRNA sequences. EPSR3 was a major fraction of exopolysaccharides (EP) containing no sulfate and had uronic acid (28.7%). The monosaccharide composition of these fractions is composed of glucose, galacturonic acid, and arabinose with a molar ratio of 2.0: 0.8: 1.0, respectively. EPSR3 was subjected to antioxidant, antitumor, and anti-inflammatory activities. The results revealed that the whole antioxidant activity was 90.4 ± 1.6% at 1500 µg/mL after 120 min. So, the IC value against DPPH radical found about 500 µg/mL after 60 min. While using HO, the scavenging activity was 75.1 ± 1.9% at 1500 µg/mL after 60 min. The IC value against HO radical found about 1500 µg/mL after 15 min. EPSR3 anticytotoxic effect on the proliferation of (Bladder carcinoma cell line) (T-24), (human breast carcinoma cell line) (MCF-7), and (human prostate carcinoma cell line) (PC-3) cells. The calculated IC50 for cell line T-24 was 121 ± 4.1 µg/mL, while the IC for cell line MCF-7 was 55.7 ± 2.3 µg/mL, and PC-3 was 61.4 ± 2.6 µg/mL. Anti-inflammatory activity was determined for EPSR3 using different methods as Lipoxygenase (LOX) inhibitory assay gave IC 12.9 ± 1.3 µg/mL. While cyclooxygenase (COX-2) inhibitory test showed 29.6 ± 0.89 µg /mL. EPSR3 showed potent inhibitory activity against methicillin-resistant (MRSA) and coagulase-negative staphylococci. The exposure times of EPSR3 for the complete inhibition of cell viability of methicillin resistant was found to be 5% at 60 min. Membrane stabilization inhibitory gave 35.4 ± 0.67 µg/mL. EPSR3 has antitumor activity with a reasonable margin of safety. The antitumor activity of EPSR3 may be attributed to its content from uronic acids with potential for cellular antioxidant and anticancer functional properties.

摘要

从沙特红海海岸分离出一株[菌株名称未给出],并根据培养特征、生化特性以及16S rRNA序列的系统发育分析进行鉴定。EPSR3是胞外多糖(EP)的主要成分,不含硫酸盐,含有糖醛酸(28.7%)。这些组分的单糖组成由葡萄糖、半乳糖醛酸和阿拉伯糖组成,摩尔比分别为2.0:0.8:1.0。对EPSR3进行了抗氧化、抗肿瘤和抗炎活性测试。结果显示,在1500μg/mL浓度下120分钟后,整体抗氧化活性为90.4±1.6%。因此,60分钟后对DPPH自由基的IC值约为500μg/mL。在使用HO时,60分钟后在1500μg/mL浓度下清除活性为75.1±1.9%。15分钟后对HO自由基的IC值约为1500μg/mL。EPSR3对(膀胱癌细胞系)(T - 24)、(人乳腺癌细胞系)(MCF - 7)和(人前列腺癌细胞系)(PC - 3)细胞的增殖具有抗细胞毒性作用。计算得出细胞系T - 24的IC50为121±4.1μg/mL,细胞系MCF - 7的IC为55.7±2.3μg/mL,PC - 3的IC为61.4±2.6μg/mL。使用不同方法测定了EPSR3的抗炎活性,脂氧合酶(LOX)抑制试验得出IC为12.9±1.3μg/mL。而环氧合酶(COX - 2)抑制试验显示为29.6±0.89μg/mL。EPSR3对耐甲氧西林金黄色葡萄球菌(MRSA)和凝固酶阴性葡萄球菌显示出强效抑制活性。发现EPSR3在60分钟时对耐甲氧西林金黄色葡萄球菌细胞活力完全抑制的暴露时间为5%。膜稳定抑制作用得出35.4±0.67μg/mL。EPSR3具有抗肿瘤活性且安全性合理。EPSR3的抗肿瘤活性可能归因于其糖醛酸含量,具有细胞抗氧化和抗癌功能特性的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a227/8874505/86ddc7022a8e/metabolites-12-00132-g001.jpg

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