Oriented in situ immobilization of a functional tyrosinase on microcrystalline cellulose effectively incorporates DOPA residues in bioengineered mussel adhesive protein. Issue 12 (29th September 2021)

• Record Type: Journal Article
• Authors: Kim, Suhyeok; Bae, Gaeun; Shin, Mincheol; Kang, Eungsu; Park, Tae Yoon; Choi, Yoo Seong; Cha, Hyung Joon
• Is Part Of: Biotechnology journal. Volume 16:Issue 12(2021)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-09-29
• Subjects: 3, 4‐Dihydroxyphenyl‐L‐alanine (DOPA) -- cellulose‐binding motif -- immobilization -- mussel adhesive protein -- tyrosinase; Biotechnology -- Periodicals; 660.605
• DOI: 10.1002/biot.202100216
• Languages: English
• ISSNs: 1860-6768

Abstract

Abstract: Background: Catechol‐containing polymers such as mussel adhesive proteins (MAPs) are attractive as biocompatible adhesive biomaterials, and the catecholic amino acid 3, 4‐dihydroxyphenyl‐L‐alanine (DOPA) is considered a key molecule in underwater mussel adhesion. Tyrosinases can specifically convert tyrosine to DOPA without any cofactors. However, their catalytic properties still need to be adjusted to minimize unwanted DOPA oxidation via their diphenolase activity and catechol instability at neutral and basic pH values in the reaction products. Methods and Results: In this work, we constructed a novel functional tyrosinase, mTyr‐CNK_CBM, by fusion of mTyr‐CNK with a cellulose‐binding motif (CBM) for oriented in situ immobilization on microcrystalline cellulose via the C‐terminal CBM without any additional purification steps. mTyr‐CNK_CBM showed optimal catalytic activity at pH 4.5–6.5 and room temperature and had a high monophenolase/diphenolase activity ratio ( V max mono/ V max di = 2.08 at pH 6 and 25°C). mTyr‐CNK_CBM exhibited 2.17‐fold higher (as a unimmobilized free enzyme) and similarly high (upon immobilization) in vitro DOPA modification of a bioengineered MAP compared to a commercially available mushroom tyrosinase. Moreover, the immobilized mTyr‐CNK_CBM showed long‐term storability and improved reusability. Conclusions: These results clearly demonstrate a strong potential for practical use of immobilized mTyr‐CNK_CBM as a monophenol monooxygenase in preparing biocompatible DOPA‐tethered biomaterials and other catechol‐containing polymers. Graphical Abstract and Lay Summary: Tyrosinases can specifically convert tyrosine to DOPA without any cofactors. However, their catalytic properties still need to be adjusted to minimize unwanted DOPA oxidation, and the enzyme should be removed after the catalytic reaction. Herein, the authors constructed a novel functional fusion tyrosinase, mTyr‐CNK_CBM, which enables oriented in situ immobilization on microcrystalline cellulose without any additional purification steps, and effectively incorporates DOPA residues in mussel adhesive protein as a model protein, demonstrating a strong potential for practical use of tyrosinases.