Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme Production
Fibrinolytic enzymes are a kind of proteolytic enzymes that can hydrolyze fibrin and dissolve blood clots. They could be used as a therapeutic agent for treating thrombosis. It is important for the treatment of cardiovascular disease to find and develop new thrombolytic drugs. In order to explore ne...
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MDPI AG
2023-04-01
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author | Zixuan He Yang Sun Min Chu Jing Zhu Yu Zhang Qiyong Tang Ghenijan Osman Ling Jiang Zhidong Zhang |
author_facet | Zixuan He Yang Sun Min Chu Jing Zhu Yu Zhang Qiyong Tang Ghenijan Osman Ling Jiang Zhidong Zhang |
author_sort | Zixuan He |
collection | DOAJ |
description | Fibrinolytic enzymes are a kind of proteolytic enzymes that can hydrolyze fibrin and dissolve blood clots. They could be used as a therapeutic agent for treating thrombosis. It is important for the treatment of cardiovascular disease to find and develop new thrombolytic drugs. In order to explore new fibrinolytic enzymes, a strain named 214L-11 with protease and fibrinolytic enzyme activity, which was isolated from the Flaming Mountain of Xinjiang Province, was screened using the skimmed milk plate, the blood powder agarose plate and the fibrin plate methods. Phylogenetic analyses showed that strain 214L-11 shared the highest similarity with <i>Streptomyces fumanus</i> NBRC 13042T (98.88%), which indicated that it represented a potential novel species in the <i>Streptomyces</i> genus. The fibrinolytic enzyme produced by 214L-11 displayed thrombolytic and anticoagulant activities, and it could degrade a single specific protein in the thrombus, thereby destroying the thrombus structure. The fermentation medium optimized through response surface methodology was 15 g/L soluble starch, g/L KNO<sub>3</sub> 0.58, 0.43 g/L peptone, 0.01 g/L FeSO<sub>4</sub>·7H<sub>2</sub>O, 0.5 g/L MgSO<sub>4</sub>·7H<sub>2</sub>O, 0.2 g/L Mn<sup>2+</sup>, 0.5 g/L NaCl and 1 L distilled water, pH 8, and the maximum amount of fibrinolytic enzyme produced by strain 214L-11 in the optimal fermentation medium was 1255.3 FU/mL. Overall, the fibrinolytic enzyme-producing strain was screened from the Flaming Mountain of Xinjiang for the first time, which provided a basis for further research and the development of new efficient and safe hemolytic drugs. |
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spelling | doaj.art-629082b5bad7447dbe0e65205532ca1e2023-11-18T01:17:23ZengMDPI AGFermentation2311-56372023-04-019541010.3390/fermentation9050410Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme ProductionZixuan He0Yang Sun1Min Chu2Jing Zhu3Yu Zhang4Qiyong Tang5Ghenijan Osman6Ling Jiang7Zhidong Zhang8Xinjiang Key Laboratory of Special Environmental Microbiology, Institute of Microbiology, Xinjiang Academy of Agricultural Sciences, Urumqi 830091, ChinaCollege of Food Science and Light Industry, Nanjing Tech University, Nanjing 211816, ChinaXinjiang Key Laboratory of Special Environmental Microbiology, Institute of Microbiology, Xinjiang Academy of Agricultural Sciences, Urumqi 830091, ChinaXinjiang Key Laboratory of Special Environmental Microbiology, Institute of Microbiology, Xinjiang Academy of Agricultural Sciences, Urumqi 830091, ChinaPlant Protection Station of Xinjiang Uygur Autonomous Region, Urumqi 830023, ChinaXinjiang Key Laboratory of Special Environmental Microbiology, Institute of Microbiology, Xinjiang Academy of Agricultural Sciences, Urumqi 830091, ChinaXinjiang Key Laboratory of Special Environmental Microbiology, Institute of Microbiology, Xinjiang Academy of Agricultural Sciences, Urumqi 830091, ChinaCollege of Food Science and Light Industry, Nanjing Tech University, Nanjing 211816, ChinaXinjiang Key Laboratory of Special Environmental Microbiology, Institute of Microbiology, Xinjiang Academy of Agricultural Sciences, Urumqi 830091, ChinaFibrinolytic enzymes are a kind of proteolytic enzymes that can hydrolyze fibrin and dissolve blood clots. They could be used as a therapeutic agent for treating thrombosis. It is important for the treatment of cardiovascular disease to find and develop new thrombolytic drugs. In order to explore new fibrinolytic enzymes, a strain named 214L-11 with protease and fibrinolytic enzyme activity, which was isolated from the Flaming Mountain of Xinjiang Province, was screened using the skimmed milk plate, the blood powder agarose plate and the fibrin plate methods. Phylogenetic analyses showed that strain 214L-11 shared the highest similarity with <i>Streptomyces fumanus</i> NBRC 13042T (98.88%), which indicated that it represented a potential novel species in the <i>Streptomyces</i> genus. The fibrinolytic enzyme produced by 214L-11 displayed thrombolytic and anticoagulant activities, and it could degrade a single specific protein in the thrombus, thereby destroying the thrombus structure. The fermentation medium optimized through response surface methodology was 15 g/L soluble starch, g/L KNO<sub>3</sub> 0.58, 0.43 g/L peptone, 0.01 g/L FeSO<sub>4</sub>·7H<sub>2</sub>O, 0.5 g/L MgSO<sub>4</sub>·7H<sub>2</sub>O, 0.2 g/L Mn<sup>2+</sup>, 0.5 g/L NaCl and 1 L distilled water, pH 8, and the maximum amount of fibrinolytic enzyme produced by strain 214L-11 in the optimal fermentation medium was 1255.3 FU/mL. Overall, the fibrinolytic enzyme-producing strain was screened from the Flaming Mountain of Xinjiang for the first time, which provided a basis for further research and the development of new efficient and safe hemolytic drugs.https://www.mdpi.com/2311-5637/9/5/410fibrinolytic enzyme<i>Streptomyces</i>anticoagulantresponse surface methodology |
spellingShingle | Zixuan He Yang Sun Min Chu Jing Zhu Yu Zhang Qiyong Tang Ghenijan Osman Ling Jiang Zhidong Zhang Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme Production Fermentation fibrinolytic enzyme <i>Streptomyces</i> anticoagulant response surface methodology |
title | Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme Production |
title_full | Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme Production |
title_fullStr | Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme Production |
title_full_unstemmed | Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme Production |
title_short | Screening of a Novel Fibrinolytic Enzyme-Producing <i>Streptomyces</i> from a Hyper-Arid Area and Optimization of Its Fibrinolytic Enzyme Production |
title_sort | screening of a novel fibrinolytic enzyme producing i streptomyces i from a hyper arid area and optimization of its fibrinolytic enzyme production |
topic | fibrinolytic enzyme <i>Streptomyces</i> anticoagulant response surface methodology |
url | https://www.mdpi.com/2311-5637/9/5/410 |
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