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This research proposes a method for separating and purifying tissue-type plasminogen activator from a fungal cell source.
This work was designed to establish methods for purifying a fibrinolytic enzyme with high purity and fibrinolytic activity from Trichoderma reesei-submerged culture liquid. Presently, the majority of tissue-type plasminogen activator (t-PA) is separated and purified from biological tissues or anima cells. Separation and purification of t-PA from genetically recombined T. reesei, a fungus, has not been reported. This research proposes a method for separating and purifying t-PA from this fungal cell source. The method, characterized by low cost, high activity recovery, and simple operation, can be applied in clinical settings.
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Submitted: April 10, 2018
Accepted: May 3, 2018
Jinhua Shao, Fulin He*, email@example.com, and Xiaoming Chen are at the School of Chemical and Biological Engineering, Hunan University of Science and Engineering; Yufei Zhang is at the Key Laboratory of Anti-fibrous Biological Therapy, MuDanjiang Medical University; and Zhiyong Zhu is at the College of Computer Science, Hunan University of Science and Engineering.
*To whom correspondence should be addressed.
Volume 31, Issue 12
When referring to this article, please cite it as J. Shao et al., “Separation and Purification of a Tissue-Type Plasminogen Activator from Trichoderma reesei,” BioPharm International 31 (12) 2018.