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Metabolic engineering of poly (3-hydroxyalkanoates): from DNA to plastic

diversity

[No authors listed]
GSID: MZOwrsXB9KoJ
LL Madison, GW Huisman - Microbiology and molecular biology …, 1999 - Am Soc Microbiol

SUMMARY Poly (3-hydroxyalkanoates)(PHAs) are a class of microbially produced polyesters that have potential applications as conventional plastics, specifically …

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Madison, L. L., & Huisman, G. W. (1999). Metabolic engineering of poly (3-hydroxyalkanoates): from DNA to plastic. Microbiology and molecular biology reviews, 63(1), 21-53.
Madison, Lara L., and Gjalt W. Huisman. "Metabolic engineering of poly (3-hydroxyalkanoates): from DNA to plastic." Microbiology and molecular biology reviews 63.1 (1999): 21-53.
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Cycloaliphatic polyester-based high-solids polyurethane coatings: II. The effect of difunctional acid

EPSCoR Research Infrastructure Improvement Program AND Program Evaluation

Soucek MD.
GSID: tdHD9PPsE_8J
H Ni, JL Daum, PR Thiltgen, MD Soucek… - Progress in organic …, 2002 - Elsevier

Two series of polyesters were synthesized with isomeric cyclohexane diacids. The first series of polyesters was synthesized with 1, 4-cyclohexanedimethanol (CHDM) and three cycloaliphatic difunctional acids, 1, 4-cyclohexanedicarboxylic acid (1, 4-CHDA), 1, 3-cyclohexanedicarboxylic acid (1, 3-CHDA), or hexahydrophthalic anhydride...

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Ni, H., Daum, J. L., Thiltgen, P. R., Soucek, M. D., Simonsick Jr, W. J., Zhong, W., & Skaja, A. D. (2002). Cycloaliphatic polyester-based high-solids polyurethane coatings: II. The effect of difunctional acid. Progress in organic coatings, 45(1), 49-58.
Ni, Hai, et al. "Cycloaliphatic polyester-based high-solids polyurethane coatings: II. The effect of difunctional acid." Progress in organic coatings 45.1 (2002): 49-58.
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Nanoparticles from renewable polymers.

Frontiers in chemistry

Wurm FR, Weiss CK.
PMID: 25101259
Front Chem. 2014 Jul 18;2:49. doi: 10.3389/fchem.2014.00049. eCollection 2014.

The use of polymers from natural resources can bring many benefits for novel polymeric nanoparticle systems. Such polymers have a variety of beneficial properties such as biodegradability and biocompatibility, they are readily available on large scale and at low...

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Wurm FR, Weiss CK. Nanoparticles from renewable polymers. Front Chem. 2014;2:49doi: 10.3389/fchem.2014.00049.
Wurm, F. R., & Weiss, C. K. (2014). Nanoparticles from renewable polymers. Frontiers in chemistry, 249. https://doi.org/10.3389/fchem.2014.00049
Wurm, Frederik R, and Weiss, Clemens K. "Nanoparticles from renewable polymers." Frontiers in chemistry vol. 2 (2014): 49. doi: https://doi.org/10.3389/fchem.2014.00049
Wurm FR, Weiss CK. Nanoparticles from renewable polymers. Front Chem. 2014 Jul 18;2:49. doi: 10.3389/fchem.2014.00049. eCollection 2014. PMID: 25101259; PMCID: PMC4102895.
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Controlled Ring-Opening Polymerization of O-Carboxyanhydrides Using a β-Diiminate Zinc Catalyst.

Angewandte Chemie (International ed. in English)

Wang R, Zhang J, Yin Q, Xu Y, Cheng J, Tong R.
PMID: 27634170
Angew Chem Int Ed Engl. 2016 Oct 10;55(42):13010-13014. doi: 10.1002/anie.201605508.

Recently O-carboxyanhydrides (OCAs) have emerged as a class of viable monomers which can undergo ring-opening polymerization (ROP) to prepare poly(α-hydroxyalkanoic acid) with functional groups that are typically difficult to achieve by ROP of lactones. Organocatalysts for the ROP of...

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Wang R, Zhang J, Yin Q, et al. Controlled Ring-Opening Polymerization of O-Carboxyanhydrides Using a β-Diiminate Zinc Catalyst. Angew Chem Int Ed Engl. 2016;55(42):13010-13014doi: 10.1002/anie.201605508.
Wang, R., Zhang, J., Yin, Q., Xu, Y., Cheng, J., & Tong, R. (2016). Controlled Ring-Opening Polymerization of O-Carboxyanhydrides Using a β-Diiminate Zinc Catalyst. Angewandte Chemie (International ed. in English), 55(42), 13010-13014. https://doi.org/10.1002/anie.201605508
Wang, Ruibo, et al. "Controlled Ring-Opening Polymerization of O-Carboxyanhydrides Using a β-Diiminate Zinc Catalyst." Angewandte Chemie (International ed. in English) vol. 55,42 (2016): 13010-13014. doi: https://doi.org/10.1002/anie.201605508
Wang R, Zhang J, Yin Q, Xu Y, Cheng J, Tong R. Controlled Ring-Opening Polymerization of O-Carboxyanhydrides Using a β-Diiminate Zinc Catalyst. Angew Chem Int Ed Engl. 2016 Oct 10;55(42):13010-13014. doi: 10.1002/anie.201605508. PMID: 27634170.
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Biodegradable PEG-Based Amphiphilic Block Copolymers for Tissue Engineering Applications.

ACS biomaterials science & engineering

Kutikov AB, Song J.
PMID: 27175443
ACS Biomater Sci Eng. 2015 Jul 13;1(7):463-480. doi: 10.1021/acsbiomaterials.5b00122. Epub 2015 May 26.

Biodegradable tissue engineering scaffolds have great potential for delivering cells/therapeutics and supporting tissue formation. Polyesters, the most extensively investigated biodegradable synthetic polymers, are not ideally suited for diverse tissue engineering applications due to limitations associated with their hydrophobicity. This...

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Kutikov AB, Song J. Biodegradable PEG-Based Amphiphilic Block Copolymers for Tissue Engineering Applications. ACS Biomater Sci Eng. 2015;1(7):463-480doi: 10.1021/acsbiomaterials.5b00122.
Kutikov, A. B., & Song, J. (2015). Biodegradable PEG-Based Amphiphilic Block Copolymers for Tissue Engineering Applications. ACS biomaterials science & engineering, 1(7), 463-480. https://doi.org/10.1021/acsbiomaterials.5b00122
Kutikov, Artem B, and Song, Jie. "Biodegradable PEG-Based Amphiphilic Block Copolymers for Tissue Engineering Applications." ACS biomaterials science & engineering vol. 1,7 (2015): 463-480. doi: https://doi.org/10.1021/acsbiomaterials.5b00122
Kutikov AB, Song J. Biodegradable PEG-Based Amphiphilic Block Copolymers for Tissue Engineering Applications. ACS Biomater Sci Eng. 2015 Jul 13;1(7):463-480. doi: 10.1021/acsbiomaterials.5b00122. Epub 2015 May 26. PMID: 27175443; PMCID: PMC4860614.
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Synthetic biodegradable functional polymers for tissue engineering: a brief review.

Science China. Chemistry

BaoLin G, Ma PX.
PMID: 25729390
Sci China Chem. 2014 Apr 01;57(4):490-500. doi: 10.1007/s11426-014-5086-y.

Scaffolds play a crucial role in tissue engineering. Biodegradable polymers with great processing flexibility are the predominant scaffolding materials. Synthetic biodegradable polymers with well-defined structure and without immunological concerns associated with naturally derived polymers are widely used in tissue...

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BaoLin G, Ma PX. Synthetic biodegradable functional polymers for tissue engineering: a brief review. Sci China Chem. 2014;57(4):490-500doi: 10.1007/s11426-014-5086-y.
BaoLin, G., & Ma, P. X. (2014). Synthetic biodegradable functional polymers for tissue engineering: a brief review. Science China. Chemistry, 57(4), 490-500. https://doi.org/10.1007/s11426-014-5086-y
BaoLin, Guo, and Ma, Peter X. "Synthetic biodegradable functional polymers for tissue engineering: a brief review." Science China. Chemistry vol. 57,4 (2014): 490-500. doi: https://doi.org/10.1007/s11426-014-5086-y
BaoLin G, Ma PX. Synthetic biodegradable functional polymers for tissue engineering: a brief review. Sci China Chem. 2014 Apr 01;57(4):490-500. doi: 10.1007/s11426-014-5086-y. PMID: 25729390; PMCID: PMC4341840.
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The effect of mechanical loads on the degradation of aliphatic biodegradable polyesters.

Regenerative biomaterials

Li Y, Chu Z, Li X, Ding X, Guo M, Zhao H, Yao J, Wang L, Cai Q, Fan Y.
PMID: 28596915
Regen Biomater. 2017 Jun;4(3):179-190. doi: 10.1093/rb/rbx009. Epub 2017 Apr 17.

Aliphatic biodegradable polyesters have been the most widely used synthetic polymers for developing biodegradable devices as alternatives for the currently used permanent medical devices. The performances during biodegradation process play crucial roles for final realization of their functions. Because...

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Li Y, Chu Z, Li X, et al. The effect of mechanical loads on the degradation of aliphatic biodegradable polyesters. Regen Biomater. 2017;4(3):179-190doi: 10.1093/rb/rbx009.
Li, Y., Chu, Z., Li, X., Ding, X., Guo, M., Zhao, H., Yao, J., Wang, L., Cai, Q., & Fan, Y. (2017). The effect of mechanical loads on the degradation of aliphatic biodegradable polyesters. Regenerative biomaterials, 4(3), 179-190. https://doi.org/10.1093/rb/rbx009
Li, Ying, et al. "The effect of mechanical loads on the degradation of aliphatic biodegradable polyesters." Regenerative biomaterials vol. 4,3 (2017): 179-190. doi: https://doi.org/10.1093/rb/rbx009
Li Y, Chu Z, Li X, Ding X, Guo M, Zhao H, Yao J, Wang L, Cai Q, Fan Y. The effect of mechanical loads on the degradation of aliphatic biodegradable polyesters. Regen Biomater. 2017 Jun;4(3):179-190. doi: 10.1093/rb/rbx009. Epub 2017 Apr 17. PMID: 28596915; PMCID: PMC5458542.
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Beyond stereoselectivity, switchable catalysis: some of the last frontier challenges in ring-opening polymerization of cyclic esters.

Chemistry (Weinheim an der Bergstrasse, Germany)

Guillaume SM, Kirillov E, Sarazin Y, Carpentier JF.
PMID: 25832549
Chemistry. 2015 May 26;21(22):7988-8003. doi: 10.1002/chem.201500613. Epub 2015 Apr 01.

Metal-based catalysts and initiators have played a pivotal role in the ring-opening polymerization (ROP) of cyclic esters, thanks to their high activity and remarkable ability to control precisely the architectures of the resulting polyesters in terms of molar mass,...

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Guillaume SM, Kirillov E, Sarazin Y, et al. Beyond stereoselectivity, switchable catalysis: some of the last frontier challenges in ring-opening polymerization of cyclic esters. Chemistry. 2015;21(22):7988-8003doi: 10.1002/chem.201500613.
Guillaume, S. M., Kirillov, E., Sarazin, Y., & Carpentier, J. F. (2015). Beyond stereoselectivity, switchable catalysis: some of the last frontier challenges in ring-opening polymerization of cyclic esters. Chemistry (Weinheim an der Bergstrasse, Germany), 21(22), 7988-8003. https://doi.org/10.1002/chem.201500613
Guillaume, Sophie M, et al. "Beyond stereoselectivity, switchable catalysis: some of the last frontier challenges in ring-opening polymerization of cyclic esters." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,22 (2015): 7988-8003. doi: https://doi.org/10.1002/chem.201500613
Guillaume SM, Kirillov E, Sarazin Y, Carpentier JF. Beyond stereoselectivity, switchable catalysis: some of the last frontier challenges in ring-opening polymerization of cyclic esters. Chemistry. 2015 May 26;21(22):7988-8003. doi: 10.1002/chem.201500613. Epub 2015 Apr 01. PMID: 25832549.
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Mass spectrometry for the elucidation of the subtle molecular structure of biodegradable polymers and their degradation products.

Mass spectrometry reviews

Kowalczuk M, Adamus G.
PMID: 25869251
Mass Spectrom Rev. 2016 Jan-Feb;35(1):188-98. doi: 10.1002/mas.21474. Epub 2015 Apr 13.

Contemporary reports by Polish authors on the application of mass spectrometric methods for the elucidation of the subtle molecular structure of biodegradable polymers and their degradation products will be presented. Special emphasis will be given to natural aliphatic (co)polyesters...

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Kowalczuk M, Adamus G. Mass spectrometry for the elucidation of the subtle molecular structure of biodegradable polymers and their degradation products. Mass Spectrom Rev. 2015;35(1):188-98doi: 10.1002/mas.21474.
Kowalczuk, M., & Adamus, G. (2016). Mass spectrometry for the elucidation of the subtle molecular structure of biodegradable polymers and their degradation products. Mass spectrometry reviews, 35(1), 188-98. https://doi.org/10.1002/mas.21474
Kowalczuk, Marek, and Adamus, Grażyna. "Mass spectrometry for the elucidation of the subtle molecular structure of biodegradable polymers and their degradation products." Mass spectrometry reviews vol. 35,1 (2016): 188-98. doi: https://doi.org/10.1002/mas.21474
Kowalczuk M, Adamus G. Mass spectrometry for the elucidation of the subtle molecular structure of biodegradable polymers and their degradation products. Mass Spectrom Rev. 2016 Jan-Feb;35(1):188-98. doi: 10.1002/mas.21474. Epub 2015 Apr 13. PMID: 25869251.
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Optical Behaviors of Cholesteric Liquid-Crystalline Polyester Composites with Various Chiral Photochromic Dopants.

Langmuir : the ACS journal of surfaces and colloids

Chien CC, Liu JH.
PMID: 26636344
Langmuir. 2015 Dec 15;31(49):13410-9. doi: 10.1021/acs.langmuir.5b03201. Epub 2015 Dec 04.

New developments in the field of chiral nematic liquid crystals, such as color displays, are now being widely proposed. This article describes the tunable incident reflection band based on composite materials of low-molecular-weight chiroptical dopants and polymeric networks. These...

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Chien CC, Liu JH. Optical Behaviors of Cholesteric Liquid-Crystalline Polyester Composites with Various Chiral Photochromic Dopants. Langmuir. 2015;31(49):13410-9doi: 10.1021/acs.langmuir.5b03201.
Chien, C. C., & Liu, J. H. (2015). Optical Behaviors of Cholesteric Liquid-Crystalline Polyester Composites with Various Chiral Photochromic Dopants. Langmuir : the ACS journal of surfaces and colloids, 31(49), 13410-9. https://doi.org/10.1021/acs.langmuir.5b03201
Chien, Chih-Chieh, and Liu, Jui-Hsiang. "Optical Behaviors of Cholesteric Liquid-Crystalline Polyester Composites with Various Chiral Photochromic Dopants." Langmuir : the ACS journal of surfaces and colloids vol. 31,49 (2015): 13410-9. doi: https://doi.org/10.1021/acs.langmuir.5b03201
Chien CC, Liu JH. Optical Behaviors of Cholesteric Liquid-Crystalline Polyester Composites with Various Chiral Photochromic Dopants. Langmuir. 2015 Dec 15;31(49):13410-9. doi: 10.1021/acs.langmuir.5b03201. Epub 2015 Dec 04. PMID: 26636344.
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Correction: One-pot atom-efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis.

Chemical communications (Cambridge, England)

Jia F, Chen X, Zheng Y, Qin Y, Tao Y, Wang X.
PMID: 26646985
Chem Commun (Camb). 2016 Jan 07;52(2):418. doi: 10.1039/c5cc90556g. Epub 2015 Dec 08.

Correction for 'One-pot atom-efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis' by Fan Jia et al., Chem. Commun., 2015, 51, 8504-8507.

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Jia F, Chen X, Zheng Y, et al. Correction: One-pot atom-efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis. Chem Commun (Camb). 2015;52(2):418doi: 10.1039/c5cc90556g.
Jia, F., Chen, X., Zheng, Y., Qin, Y., Tao, Y., & Wang, X. (2016). Correction: One-pot atom-efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis. Chemical communications (Cambridge, England), 52(2), 418. https://doi.org/10.1039/c5cc90556g
Jia, Fan, et al. "Correction: One-pot atom-efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis." Chemical communications (Cambridge, England) vol. 52,2 (2016): 418. doi: https://doi.org/10.1039/c5cc90556g
Jia F, Chen X, Zheng Y, Qin Y, Tao Y, Wang X. Correction: One-pot atom-efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis. Chem Commun (Camb). 2016 Jan 07;52(2):418. doi: 10.1039/c5cc90556g. Epub 2015 Dec 08. PMID: 26646985.
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Data on synthesis of oligomeric and polymeric poly(butylene adipate-co-butylene terephthalate) model substrates for the investigation of enzymatic hydrolysis.

Data in brief

Perz V, Bleymaier K, Sinkel C, Kueper U, Bonnekessel M, Ribitsch D, Guebitz GM.
PMID: 26981550
Data Brief. 2016 Feb 19;7:291-8. doi: 10.1016/j.dib.2016.02.029. eCollection 2016 Jun.

The aliphatic-aromatic copolyester poly(butylene adipate-co-butylene terephthalate) (PBAT), also known as ecoflex, contains adipic acid, 1,4-butanediol and terephthalic acid and is proven to be compostable [1], [2], [3]). We describe here data for the synthesis and analysis of poly(butylene adipate-co-butylene...

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Perz V, Bleymaier K, Sinkel C, et al. Data on synthesis of oligomeric and polymeric poly(butylene adipate-co-butylene terephthalate) model substrates for the investigation of enzymatic hydrolysis. Data Brief. 2016;7:291-8doi: 10.1016/j.dib.2016.02.029.
Perz, V., Bleymaier, K., Sinkel, C., Kueper, U., Bonnekessel, M., Ribitsch, D., & Guebitz, G. M. (2016). Data on synthesis of oligomeric and polymeric poly(butylene adipate-co-butylene terephthalate) model substrates for the investigation of enzymatic hydrolysis. Data in brief, 7291-8. https://doi.org/10.1016/j.dib.2016.02.029
Perz, Veronika, et al. "Data on synthesis of oligomeric and polymeric poly(butylene adipate-co-butylene terephthalate) model substrates for the investigation of enzymatic hydrolysis." Data in brief vol. 7 (2016): 291-8. doi: https://doi.org/10.1016/j.dib.2016.02.029
Perz V, Bleymaier K, Sinkel C, Kueper U, Bonnekessel M, Ribitsch D, Guebitz GM. Data on synthesis of oligomeric and polymeric poly(butylene adipate-co-butylene terephthalate) model substrates for the investigation of enzymatic hydrolysis. Data Brief. 2016 Feb 19;7:291-8. doi: 10.1016/j.dib.2016.02.029. eCollection 2016 Jun. PMID: 26981550; PMCID: PMC4776266.
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Showing 1 to 12 of 608 entries