Ghfren S. Aloraini, Mona Othman I. Albureikan, Aisha M. A. Shahlol, Taghreed Shamrani, Hussam Daghistani, Mohammad El-Nablaway, Nagwa A. Tharwat, Ahmed M. Elazzazy, Ahmed F. Basyony, Ahmed Ghareeb
{"title":"海洋假单胞菌菌株 AHG22 外多糖的生物医学和治疗潜力:一种新型生物活性微生物代谢物","authors":"Ghfren S. Aloraini, Mona Othman I. Albureikan, Aisha M. A. Shahlol, Taghreed Shamrani, Hussam Daghistani, Mohammad El-Nablaway, Nagwa A. Tharwat, Ahmed M. Elazzazy, Ahmed F. Basyony, Ahmed Ghareeb","doi":"10.1515/rams-2024-0016","DOIUrl":null,"url":null,"abstract":"Microbial exopolysaccharides (EPSs) are gaining interest as alternatives to chemical antioxidants and pharmaceuticals. This study mines the promising biomedical and antimicrobial potential of a marine bacterium, a prolific EPS producer, isolated from the Red Sea. <jats:italic>Pseudomonas</jats:italic> sp. strain AHG22 generated an EPS weighing 6.98 g·L<jats:sup>−1</jats:sup>, coded EPSF8, subjected to FT-IR and HPLC chemical analysis. EPSF8 was then investigated for antioxidant assessment by 2,2-diphenyl-1-picrylhydrazyl (DPPH), H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>, ABTS˙<jats:sup> + </jats:sup>, nitric oxide, total antioxidant capacity (TAC), and ferric reducing antioxidant power (FRAP). EPSF8 had an IC<jats:sub>50</jats:sub> of 46.99 μg·mL<jats:sup>−1</jats:sup> in the DPPH antioxidant assay and antioxidant capacities of 219.45 μg·mg<jats:sup>−1</jats:sup> ascorbic acid equivalent (AAE) in the TAC assay and 54.15 μg·mg<jats:sup>−1</jats:sup> AAE in the FRAP assay. The <jats:italic>in vitro</jats:italic> anti-inflammatory effect of EPSF8 was tested against 5-lipoxygenase (5-LOX) and cyclooxygenase-2 (COX-2) enzymes and compared with the drugs ibuprofen and celecoxib used as controls. The IC<jats:sub>50</jats:sub> values of 5-LOX, COX-2, ibuprofen, and celecoxib were found to be 14.82, 15.49, 1.5, and 0.28 μg·mL<jats:sup>−1</jats:sup>, respectively. Additionally, EPSF8 revealed antidiabetic activity toward α-amylase and α-glucosidase, and the IC<jats:sub>50</jats:sub> values were 93.1 and 127.28 μg·mL<jats:sup>−1</jats:sup>, compared to those of acarbose (50.93 and 4.13 μg·mL<jats:sup>−1</jats:sup>, respectively). Anti-obesity activity of EPSF8 by lipase inhibition revealed IC<jats:sub>50</jats:sub> = 56.12 μg·mL<jats:sup>−1</jats:sup> compared to orlistat (IC<jats:sub>50</jats:sub> = 20.08 μg·mL<jats:sup>−1</jats:sup>) as a control. EPSF8 displayed antibiofilm and bactericidal activity against Gram-positive (G +ve) and Gram-negative (G −ve) ATCC pathogenic bacterial strains. It had a minimum bactericidal concentration/minimum inhibitory concentration ratio ≤2, indicating a broad bactericidal spectrum. Furthermore, EPSF8 is evidenced to have a promising anti-butyrylcholinesterase activity for the control of Alzheimer’s disease. The findings of the present analysis suggest that the isolated <jats:italic>Pseudomonas</jats:italic> sp. strain AHG22 EPS can potentially be explored as a promising green therapeutic compound.","PeriodicalId":54484,"journal":{"name":"Reviews on Advanced Materials Science","volume":"86 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biomedical and therapeutic potential of marine-derived Pseudomonas sp. strain AHG22 exopolysaccharide: A novel bioactive microbial metabolite\",\"authors\":\"Ghfren S. Aloraini, Mona Othman I. Albureikan, Aisha M. A. Shahlol, Taghreed Shamrani, Hussam Daghistani, Mohammad El-Nablaway, Nagwa A. Tharwat, Ahmed M. Elazzazy, Ahmed F. Basyony, Ahmed Ghareeb\",\"doi\":\"10.1515/rams-2024-0016\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Microbial exopolysaccharides (EPSs) are gaining interest as alternatives to chemical antioxidants and pharmaceuticals. This study mines the promising biomedical and antimicrobial potential of a marine bacterium, a prolific EPS producer, isolated from the Red Sea. <jats:italic>Pseudomonas</jats:italic> sp. strain AHG22 generated an EPS weighing 6.98 g·L<jats:sup>−1</jats:sup>, coded EPSF8, subjected to FT-IR and HPLC chemical analysis. EPSF8 was then investigated for antioxidant assessment by 2,2-diphenyl-1-picrylhydrazyl (DPPH), H<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>, ABTS˙<jats:sup> + </jats:sup>, nitric oxide, total antioxidant capacity (TAC), and ferric reducing antioxidant power (FRAP). EPSF8 had an IC<jats:sub>50</jats:sub> of 46.99 μg·mL<jats:sup>−1</jats:sup> in the DPPH antioxidant assay and antioxidant capacities of 219.45 μg·mg<jats:sup>−1</jats:sup> ascorbic acid equivalent (AAE) in the TAC assay and 54.15 μg·mg<jats:sup>−1</jats:sup> AAE in the FRAP assay. The <jats:italic>in vitro</jats:italic> anti-inflammatory effect of EPSF8 was tested against 5-lipoxygenase (5-LOX) and cyclooxygenase-2 (COX-2) enzymes and compared with the drugs ibuprofen and celecoxib used as controls. The IC<jats:sub>50</jats:sub> values of 5-LOX, COX-2, ibuprofen, and celecoxib were found to be 14.82, 15.49, 1.5, and 0.28 μg·mL<jats:sup>−1</jats:sup>, respectively. Additionally, EPSF8 revealed antidiabetic activity toward α-amylase and α-glucosidase, and the IC<jats:sub>50</jats:sub> values were 93.1 and 127.28 μg·mL<jats:sup>−1</jats:sup>, compared to those of acarbose (50.93 and 4.13 μg·mL<jats:sup>−1</jats:sup>, respectively). Anti-obesity activity of EPSF8 by lipase inhibition revealed IC<jats:sub>50</jats:sub> = 56.12 μg·mL<jats:sup>−1</jats:sup> compared to orlistat (IC<jats:sub>50</jats:sub> = 20.08 μg·mL<jats:sup>−1</jats:sup>) as a control. EPSF8 displayed antibiofilm and bactericidal activity against Gram-positive (G +ve) and Gram-negative (G −ve) ATCC pathogenic bacterial strains. It had a minimum bactericidal concentration/minimum inhibitory concentration ratio ≤2, indicating a broad bactericidal spectrum. Furthermore, EPSF8 is evidenced to have a promising anti-butyrylcholinesterase activity for the control of Alzheimer’s disease. 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Biomedical and therapeutic potential of marine-derived Pseudomonas sp. strain AHG22 exopolysaccharide: A novel bioactive microbial metabolite
Microbial exopolysaccharides (EPSs) are gaining interest as alternatives to chemical antioxidants and pharmaceuticals. This study mines the promising biomedical and antimicrobial potential of a marine bacterium, a prolific EPS producer, isolated from the Red Sea. Pseudomonas sp. strain AHG22 generated an EPS weighing 6.98 g·L−1, coded EPSF8, subjected to FT-IR and HPLC chemical analysis. EPSF8 was then investigated for antioxidant assessment by 2,2-diphenyl-1-picrylhydrazyl (DPPH), H2O2, ABTS˙ + , nitric oxide, total antioxidant capacity (TAC), and ferric reducing antioxidant power (FRAP). EPSF8 had an IC50 of 46.99 μg·mL−1 in the DPPH antioxidant assay and antioxidant capacities of 219.45 μg·mg−1 ascorbic acid equivalent (AAE) in the TAC assay and 54.15 μg·mg−1 AAE in the FRAP assay. The in vitro anti-inflammatory effect of EPSF8 was tested against 5-lipoxygenase (5-LOX) and cyclooxygenase-2 (COX-2) enzymes and compared with the drugs ibuprofen and celecoxib used as controls. The IC50 values of 5-LOX, COX-2, ibuprofen, and celecoxib were found to be 14.82, 15.49, 1.5, and 0.28 μg·mL−1, respectively. Additionally, EPSF8 revealed antidiabetic activity toward α-amylase and α-glucosidase, and the IC50 values were 93.1 and 127.28 μg·mL−1, compared to those of acarbose (50.93 and 4.13 μg·mL−1, respectively). Anti-obesity activity of EPSF8 by lipase inhibition revealed IC50 = 56.12 μg·mL−1 compared to orlistat (IC50 = 20.08 μg·mL−1) as a control. EPSF8 displayed antibiofilm and bactericidal activity against Gram-positive (G +ve) and Gram-negative (G −ve) ATCC pathogenic bacterial strains. It had a minimum bactericidal concentration/minimum inhibitory concentration ratio ≤2, indicating a broad bactericidal spectrum. Furthermore, EPSF8 is evidenced to have a promising anti-butyrylcholinesterase activity for the control of Alzheimer’s disease. The findings of the present analysis suggest that the isolated Pseudomonas sp. strain AHG22 EPS can potentially be explored as a promising green therapeutic compound.
期刊介绍:
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