Literature DB >> 23688291

One-pot microbial production, mechanical properties, and enzymatic degradation of isotactic P[(R)-2-hydroxybutyrate] and its copolymer with (R)-lactate.

Ken'ichiro Matsumoto1, Satsuki Terai, Ayako Ishiyama, Jian Sun, Taizo Kabe, Yuyang Song, John Masani Nduko, Tadahisa Iwata, Seiichi Taguchi.   

Abstract

P[(R)-2-hydroxybutyrate] [P((R)-2HB)] is an aliphatic polyester analogous to poly(lactic acid) (PLA). However, little has been known for its properties because of a high cost of commercially available chiral 2HB as a starting substance for chemical polymer synthesis. In this study, P[(R)-2HB] and P[(R)-2HB-co-(R)-lactate] [P((R)-2HB-co-(R)-LA)] with a new monomer combination were successfully synthesized in recombinant Escherichia coli LS5218 from less-expensive racemic 2HB using an R-specific polyester synthase. The cells expressing an engineered polyhydroxyalkanoate synthase from Pseudomonas sp. 61-3 and propionyl-CoA transferase from Megasphaera elsdenii were grown on LB medium containing 2HB and glucose in a shake flask and accumulated up to 17 wt % of P[(R)-2HB] with optical purity of >99.1%. In addition, the same cells cultured in a jar-fermentor produced P(86 mol % 2HB-co-LA) copolymer. Notably, the molecular weights (Mw) of P(2HB) (27000) and P(2HB-co-LA) (39000) were 2- and 3-fold higher than that of P(2HB) previously synthesized by chemical polycondensation. P(2HB) was processed into a transparent film by solvent-casting and it had flexible properties with elongation at break of 173%, which was contrast to the rigid PLA. Regarding mechanical properties, P(2HB-co-LA) was tougher but less stretchy than P(2HB). These results demonstrated that P(2HB) has useful properties and LA units in 2HB-based polymers can act as a controllable modulator of the material properties. In addition, P[(R)-2HB] was efficiently degraded by treatment of Novozym 42044 (lipase) but not Savinase 16L (protease), indicating that the degrading behavior of the polymer was similar to that of P[(R)-LA].

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Year:  2013        PMID: 23688291     DOI: 10.1021/bm400278j

Source DB:  PubMed          Journal:  Biomacromolecules        ISSN: 1525-7797            Impact factor:   6.988


  6 in total

1.  Versatile aliphatic polyester biosynthesis system for producing random and block copolymers composed of 2-, 3-, 4-, 5-, and 6-hydroxyalkanoates using the sequence-regulating polyhydroxyalkanoate synthase PhaCAR.

Authors:  Tomoya Kawakami; Nagi Isobe; Loïc Pasquier; Keigo Satoh; Hiroya Tomita; Manfred Zinn; Ken'ichiro Matsumoto
Journal:  Microb Cell Fact       Date:  2022-05-14       Impact factor: 6.352

2.  MtgA Deletion-Triggered Cell Enlargement of Escherichia coli for Enhanced Intracellular Polyester Accumulation.

Authors:  Ryosuke Kadoya; Ken'ichiro Matsumoto; Toshihiko Ooi; Seiichi Taguchi
Journal:  PLoS One       Date:  2015-06-03       Impact factor: 3.240

3.  Engineering the xylose-catabolizing Dahms pathway for production of poly(d-lactate-co-glycolate) and poly(d-lactate-co-glycolate-co-d-2-hydroxybutyrate) in Escherichia coli.

Authors:  So Young Choi; Won Jun Kim; Seung Jung Yu; Si Jae Park; Sung Gap Im; Sang Yup Lee
Journal:  Microb Biotechnol       Date:  2017-04-19       Impact factor: 5.813

4.  Increased Production and Molecular Weight of Artificial Polyhydroxyalkanoate Poly(2-hydroxybutyrate) Above the Glass Transition Temperature Threshold.

Authors:  Ken'ichiro Matsumoto; Yuki Kageyama
Journal:  Front Bioeng Biotechnol       Date:  2019-07-24

5.  Artificial polyhydroxyalkanoate poly[2-hydroxybutyrate-block-3-hydroxybutyrate] elastomer-like material.

Authors:  Yuki Kageyama; Hiroya Tomita; Takuya Isono; Toshifumi Satoh; Ken'ichiro Matsumoto
Journal:  Sci Rep       Date:  2021-11-17       Impact factor: 4.379

6.  Synthesis and stereocomplex formation of enantiomeric alternating copolymers with two types of chiral centers, poly(lactic acid-alt-2-hydroxybutanoic acid)s.

Authors:  Hideto Tsuji; Kazuya Nakayama; Yuki Arakawa
Journal:  RSC Adv       Date:  2020-10-23       Impact factor: 4.036

  6 in total

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