Exopolysaccharide isolated from marine Bacillus subtilis strain AF2: production, characterization, purification and in vitro bioactivity.

IF 2.1 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Mohamed F Assar, Sahar S Mohamed, Mohamed Ali, Mahmoud I Afify, Mohamed E El Awady
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Abstract

Bacillus subtilis strain AF2 was obtained from the Mediterranean Sea and its identification was determined by its phylogenetic analysis of 16S rRNA sequences, as well as their morphological, physiological, and biochemical characteristics. The isolate yielded EPSS4 at a concentration of 7.4 g/l. EPSS4 constituted a significant proportion of the EPS recovered through purification using DEAE-Cellulose. The sample consisted of sulfate (24.71%) and uronic acid (18.55%). The fraction's viscosity was measured to be 1.1 mm2/sec, and the total hexose amine content was measured to be 9.06%. The monosaccharide composition of this fraction consists of glucose, fructose, xylose, and glucuronic acid in a molar ratio of 1.0:0.5:1.0:1.0, respectively. The toxicity studies on EPSS4 demonstrated its safety at 5 g/kg doses. EPSS4 underwent evaluation for its antioxidant, anticancer, and anti-inflammatory properties. The results indicated that the antioxidant activity percentages were as follows: 85.17 ± 0.77% for DPPH, 79.63 ± 1.05% for ABTS, 52.20 ± 0.67% for Fe2+ ion chelation ability, 75.80 ± 0.28% for Lipid peroxidation Inhibition capacity, 84.66 ± 1.21% for O2- radicals scavenging capacity, and 55.09 ± 0.34% for NO scavenging capacity. The IC50 value of EPSS4 for HepG-2 is 238.05 µg/ml. A-549 has determined the IC50 values to be 102.71 µg/ml. The concentration of HCT-116 was measured to be 328.01 µg/ml, while the IC50 value for the MCF-7 cell line was determined to be 204.77 µg/ml. The IC50 values for the HEP-2 and PC-3 cell lines were 118.95 and 128.94 µg/ml, respectively. The anti-inflammatory activity of EPSS4 was assessed using various methods, including measuring its inhibitory effects on lipoxygenase (LOX) and cyclooxygenase (COX2). At a dosage of 100 µg/ml, EPSS4 had a LOX inhibitory activity of 80.54 ± 1.09% and a COX2 inhibitory activity of 84.70 ± 1.05%. Due to its antioxidant capabilities, the EPS produced from Bacillus subtilis strain AF2 is a promising option for application as a potent antioxidant agent in the healthcare system. So, from observed activities demonstrate that it has the potential to be employed as an anticancer, antioxidant and non-steroidal anti-inflammatory substance via improving adaptive immune responses.

海洋枯草芽孢杆菌AF2胞外多糖的制备、鉴定、纯化及体外生物活性研究。
枯草芽孢杆菌AF2菌株来源于地中海,通过对其16S rRNA序列的系统发育分析及其形态、生理和生化特征确定其鉴定。分离得到的EPSS4浓度为7.4 g/l。通过DEAE-Cellulose纯化得到的EPS中,EPSS4占很大比例。样品主要成分为硫酸根(24.71%)和脲酸(18.55%)。测得该馏分粘度为1.1 mm2/sec,总己糖胺含量为9.06%。该部分的单糖组成由葡萄糖、果糖、木糖和葡萄糖醛酸组成,摩尔比分别为1.0:0.5:1.0:1.0。EPSS4的毒性研究表明其在5 g/kg剂量下是安全的。EPSS4对其抗氧化、抗癌和抗炎特性进行了评估。结果表明:DPPH的抗氧化能力为85.17±0.77%,ABTS的抗氧化能力为79.63±1.05%,Fe2+螯合能力为52.20±0.67%,脂质过氧化抑制能力为75.80±0.28%,O2自由基清除能力为84.66±1.21%,NO清除能力为55.09±0.34%。EPSS4对HepG-2的IC50值为238.05µg/ml。A-549测定的IC50值为102.71µg/ml。测定HCT-116的浓度为328.01µg/ml,测定MCF-7细胞株的IC50值为204.77µg/ml。HEP-2和PC-3细胞株的IC50值分别为118.95µg/ml和128.94µg/ml。采用多种方法评估EPSS4的抗炎活性,包括测定其对脂氧合酶(LOX)和环氧合酶(COX2)的抑制作用。在剂量为100µg/ml时,EPSS4对LOX的抑制活性为80.54±1.09%,对COX2的抑制活性为84.70±1.05%。由于其抗氧化能力,枯草芽孢杆菌菌株AF2产生的EPS作为一种有效的抗氧化剂在医疗保健系统中的应用是一个很有前途的选择。因此,从观察到的活性来看,它有可能通过改善适应性免疫反应而被用作抗癌、抗氧化和非甾体抗炎物质。
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来源期刊
Biotechnology Letters
Biotechnology Letters 工程技术-生物工程与应用微生物
CiteScore
5.90
自引率
3.70%
发文量
108
审稿时长
1.2 months
期刊介绍: Biotechnology Letters is the world’s leading rapid-publication primary journal dedicated to biotechnology as a whole – that is to topics relating to actual or potential applications of biological reactions affected by microbial, plant or animal cells and biocatalysts derived from them. All relevant aspects of molecular biology, genetics and cell biochemistry, of process and reactor design, of pre- and post-treatment steps, and of manufacturing or service operations are therefore included. Contributions from industrial and academic laboratories are equally welcome. We also welcome contributions covering biotechnological aspects of regenerative medicine and biomaterials and also cancer biotechnology. Criteria for the acceptance of papers relate to our aim of publishing useful and informative results that will be of value to other workers in related fields. The emphasis is very much on novelty and immediacy in order to justify rapid publication of authors’ results. It should be noted, however, that we do not normally publish papers (but this is not absolute) that deal with unidentified consortia of microorganisms (e.g. as in activated sludge) as these results may not be easily reproducible in other laboratories. Papers describing the isolation and identification of microorganisms are not regarded as appropriate but such information can be appended as supporting information to a paper. Papers dealing with simple process development are usually considered to lack sufficient novelty or interest to warrant publication.
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