Directed Evolution of Hyaluronic Acid Synthase from Pasteurella multocida towards High-Molecular-Weight Hyaluronic Acid

被引:38
|
作者
Mandawe, John [1 ,2 ]
Infanzon, Belen [3 ]
Eisele, Anna [4 ]
Zaun, Henning [5 ]
Kuballa, Juergen [5 ]
Davari, Mehdi D. [2 ]
Jakob, Felix [1 ]
Elling, Lothar [4 ]
Schwaneberg, Ulrich [1 ,2 ]
机构
[1] DWI Leibniz Inst Interact Mat, Forckenbeckstr 50, D-52056 Aachen, Germany
[2] Rhein Westfal TH Aachen, Inst Biotechnol, Worringerweg 3, D-52074 Aachen, Germany
[3] Univ Barcelona, Dept Microbiol, Fac Biol, Avinguda Diagonal 643, E-08028 Barcelona, Spain
[4] Rhein Westfal TH Aachen, Helmholtz Inst Biomed Engn, Pauwelsstr 20, D-52074 Aachen, Germany
[5] GALAB Labs GmbH, Schleusengraben 7, D-21029 Hamburg, Germany
关键词
directed evolution; hyaluronan; molecular modeling; polymerase chain reaction; protein engineering; synthases; 2; ACTIVE-SITES; BACILLUS-SUBTILIS; ESCHERICHIA-COLI; STREPTOCOCCUS-ZOOPPIDEMICUS; 3-DIMENSIONAL STRUCTURES; CULTURE-CONDITIONS; PRODUCT SIZE; FORCE-FIELD; GLYCOSYLTRANSFERASES; POLYSACCHARIDE;
D O I
10.1002/cbic.201800093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hyaluronic acid (HA), with diverse cosmetic and medical applications, is the natural glycosaminoglycan product of HA synthases. Although process and/or metabolic engineering are used for industrial HA production, the potential of protein engineering has barely been realised. Herein, knowledge-gaining directed evolution (KnowVolution) was employed to generate an HA synthase variant from Pasteurella multocida (pmHAS) with improved chain-length specificity and a twofold increase in mass-based turnover number. Seven improved pmHAS variants out of 1392 generated by error-prone PCR were identified; eight prospective positions were saturated and the most beneficial amino acid substitutions were recombined. After one round of KnowVolution, the longest HA polymer (<4.7MDa), through an engineered pmHAS variant in a cell-free system, was synthesised. Computational studies showed that substitutions from the best variant (T40L, V59M and T104A) are distant from the glycosyltransferase sites and increase the flexibility of the N-terminal region of pmHAS. Taken together, these findings suggest that the Nterminus may be involved in HA synthesis and demonstrate the potential of protein engineering towards improved HA synthase activity.
引用
收藏
页码:1414 / 1423
页数:10
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