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Volumn 10, Issue 3, 2015, Pages

Transesterification of PHA to oligomers covalently bonded with (bio)active compounds containing either carboxyl or hydroxyl functionalities

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYL GROUP; HYDROXYL GROUP; OLIGOMER; POLY(3 HYDROXYBUTYRIC ACID); POLYESTER; POLYHYDROXYALKANOIC ACID; BIODEGRADABLE PLASTIC; HYDROXYBUTYRIC ACID; POLY-BETA-HYDROXYBUTYRATE;

EID: 84925003312     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0120149     Document Type: Article
Times cited : (23)

References (30)
  • 1
    • 0028994480 scopus 로고
    • Some problems associated with the analysis of the costs and benefits of pesticides
    • Bowles RG, Webster JPG. Some problems associated with the analysis of the costs and benefits of pesticides. Crop Prot. 1995; 14: 593-600.
    • (1995) Crop Prot , vol.14 , pp. 593-600
    • Bowles, R.G.1    Webster, J.P.G.2
  • 5
    • 80051663468 scopus 로고    scopus 로고
    • Poly(hydroxybutyrate-cohydroxyvalerate) microspheres loaded with atrazine herbicide: Screening of conditions for preparation, physico-chemical characterization, and in vitro release studies
    • Lobo FA, deAguirre CL, Silva MS, Grillo R, deMelo NFS, deOliveira LK, et al. Poly(hydroxybutyrate-cohydroxyvalerate) microspheres loaded with atrazine herbicide: screening of conditions for preparation, physico-chemical characterization, and in vitro release studies. Polym Bull. 2011; 67: 479-495.
    • (2011) Polym Bull , vol.67 , pp. 479-495
    • Lobo, F.A.1    DeAguirre, C.L.2    Silva, M.S.3    Grillo, R.4    DeMelo, N.F.S.5    DeOliveira, L.K.6
  • 7
    • 84874886020 scopus 로고    scopus 로고
    • Biosynthesis and characterization of diblock copolymer of p(3-hydroxypropionate)-block-p(4-hydroxybutyrate) from recombinant escherichia coli
    • PMID: 23351169
    • Lakshmi T, Lin-PingW, Dechuan M, Jinchun C, Guo-Qiang C. Biosynthesis and characterization of diblock copolymer of p(3-hydroxypropionate)-block-p(4-hydroxybutyrate) from recombinant escherichia coli. Biomacromolecules. 2013; 14: 862-870. doi: 10.1021/bm3019517 PMID: 23351169
    • (2013) Biomacromolecules , vol.14 , pp. 862-870
    • Lakshmi, T.1    Lin-Ping, W.2    Dechuan, M.3    Jinchun, C.4    Guo-Qiang, C.5
  • 8
    • 84866061935 scopus 로고    scopus 로고
    • Biosynthesis of poly[(R)-3-hydroxyalkanoate] copolymers with controlled repeating unit compositions and physical properties
    • PMID: 22873826
    • Tappel RC, Kucharski JM, Mastroianni JM, Stipanovic AJ, Nomura CT. Biosynthesis of poly[(R)-3-hydroxyalkanoate] copolymers with controlled repeating unit compositions and physical properties. Biomacromolecules. 2012; 13: 2964-2972. doi: 10.1021/bm301043t PMID: 22873826
    • (2012) Biomacromolecules , vol.13 , pp. 2964-2972
    • Tappel, R.C.1    Kucharski, J.M.2    Mastroianni, J.M.3    Stipanovic, A.J.4    Nomura, C.T.5
  • 9
    • 84866060734 scopus 로고    scopus 로고
    • Biosynthesis and properties of medium-chain-length polyhydroxyalkanoates with enriched content of the dominant monomer
    • PMID: 22871146
    • Jiang X, Sun Z, Marchessault RH, Ramsay JA, Ramsay BA. Biosynthesis and properties of medium-chain-length polyhydroxyalkanoates with enriched content of the dominant monomer. Biomacromolecules. 2012; 13: 2926-2932. doi: 10.1021/bm3009507 PMID: 22871146
    • (2012) Biomacromolecules , vol.13 , pp. 2926-2932
    • Jiang, X.1    Sun, Z.2    Marchessault, R.H.3    Ramsay, J.A.4    Ramsay, B.A.5
  • 10
    • 0035795567 scopus 로고    scopus 로고
    • Synthesis of copolyesters consisting of me-dium-chain-length β-hydroxyalkanoates by Pseudomonas stutzeri 1317
    • Guo-Qiang C, Jun X, Qiong W, Zengming Z, Kwok-Ping H. Synthesis of copolyesters consisting of me-dium-chain-length β-hydroxyalkanoates by Pseudomonas stutzeri 1317. React Funct Polym. 2001; 48: 107-112.
    • (2001) React Funct Polym , vol.48 , pp. 107-112
    • Guo-Qiang, C.1    Jun, X.2    Qiong, W.3    Zengming, Z.4    Kwok-Ping, H.5
  • 11
    • 84885387849 scopus 로고    scopus 로고
    • Biodegradable latexes from animal-derived waste: Biosynthesis and characterization of mcl-PHA accumulated by Ps. citronellolis
    • Muhr A, Rechberger EM, Salerno A, Reiterer A, Schiller M, Kwiecień M, et al. Biodegradable latexes from animal-derived waste: Biosynthesis and characterization of mcl-PHA accumulated by Ps. citronellolis. React Funct Polym. 2013; 73: 1391-1398.
    • (2013) React Funct Polym , vol.73 , pp. 1391-1398
    • Muhr, A.1    Rechberger, E.M.2    Salerno, A.3    Reiterer, A.4    Schiller, M.5    Kwiecień, M.6
  • 12
    • 69249092516 scopus 로고    scopus 로고
    • A microbial polyhydroxyalkanoates (PHA) based bio- and materials industry
    • PMID: 19623359
    • Guo-Qiang C. A microbial polyhydroxyalkanoates (PHA) based bio- and materials industry. Chem Soc Rev. 2009; 38: 2434-2446. doi: 10.1039/b812677c PMID: 19623359
    • (2009) Chem Soc Rev , vol.38 , pp. 2434-2446
    • Guo-Qiang, C.1
  • 13
    • 84868350271 scopus 로고    scopus 로고
    • Electrospray ionisation mass spectrometry molecular-level structural characterisation of novel phenoxycarboxylic acid-oligo(3-hydroxybutyrate) conjugates with potential agricultural applications
    • PMID: 23124657
    • Kwiecień I, Adamus G, Kowalczuk M. Electrospray ionisation mass spectrometry molecular-level structural characterisation of novel phenoxycarboxylic acid-oligo(3-hydroxybutyrate) conjugates with potential agricultural applications. Rapid Commun Mass Spectrom. 2012; 26: 2673-2682. doi: 10.1002/rcm.6391 PMID: 23124657
    • (2012) Rapid Commun Mass Spectrom , vol.26 , pp. 2673-2682
    • Kwiecień, I.1    Adamus, G.2    Kowalczuk, M.3
  • 14
    • 84868019732 scopus 로고    scopus 로고
    • Synthesis and evaluation of effectiveness of a controlled release preparation 2,4-D: A reduction of risk of pollution and exposure of workers
    • Kowalski WJ, Romanowska I, Smol M, Siłowiecki A, Głazek M. Synthesis and evaluation of effectiveness of a controlled release preparation 2,4-D: a reduction of risk of pollution and exposure of workers. Arch Environ Prot. 2012; 38: 117-127.
    • (2012) Arch Environ Prot , vol.38 , pp. 117-127
    • Kowalski, W.J.1    Romanowska, I.2    Smol, M.3    Siłowiecki, A.4    Głazek, M.5
  • 16
    • 33748225163 scopus 로고
    • The triolide of (R)-3-hydroxybutyric acid - direct preparation from polyhydroxybutyrate and formation of a crown estercarbonyl complex with Na ions
    • Seebach D, Müller HM, Bürger HM, Plattner D. The triolide of (R)-3-hydroxybutyric acid - direct preparation from polyhydroxybutyrate and formation of a crown estercarbonyl complex with Na ions. Angew Chem Int Ed Engl. 1992; 31: 434-435.
    • (1992) Angew Chem Int Ed Engl , vol.31 , pp. 434-435
    • Seebach, D.1    Müller, H.M.2    Bürger, H.M.3    Plattner, D.4
  • 17
    • 0036060675 scopus 로고    scopus 로고
    • Acid catalyzed transesterification as a route to poly(3-hydroxybutyrate-co-ε-caprolactone) copolymers from their momopolymers
    • PMID: 12099830
    • Impallomeni G, Giuffrida M, Barbuzzi T, Musumarra G, Ballistreri A. Acid catalyzed transesterification as a route to poly(3-hydroxybutyrate-co-ε-caprolactone) copolymers from their momopolymers. Biomacromolecules. 2002; 3: 835-840. PMID: 12099830
    • (2002) Biomacromolecules , vol.3 , pp. 835-840
    • Impallomeni, G.1    Giuffrida, M.2    Barbuzzi, T.3    Musumarra, G.4    Ballistreri, A.5
  • 18
    • 33644661955 scopus 로고    scopus 로고
    • Matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry with size-exclusion chromatographic fractionation for structural characterization of synthetic aliphatic copolyesters
    • PMID: 16470727
    • Adamus G, Rizzarelli P, Montaudo MS, Kowalczuk M, Montaudo G. Matrix-assisted laser desorption/ ionization time-of-flight mass spectrometry with size-exclusion chromatographic fractionation for structural characterization of synthetic aliphatic copolyesters. Rapid Commun Mass Spectrom. 2006; 20: 804-814. PMID: 16470727
    • (2006) Rapid Commun Mass Spectrom , vol.20 , pp. 804-814
    • Adamus, G.1    Rizzarelli, P.2    Montaudo, M.S.3    Kowalczuk, M.4    Montaudo, G.5
  • 19
    • 0009739274 scopus 로고    scopus 로고
    • Lipase-catalyzed transformation of unnaturaltype poly(3-hydroxybutanoate) into reactive cyclic oligomer
    • Osanai Y, Toshima K, Yoshie N, Inoue Y, Matsumura S. Lipase-catalyzed transformation of unnaturaltype poly(3-hydroxybutanoate) into reactive cyclic oligomer. Macromol Biosci. 2002; 2: 88-94.
    • (2002) Macromol Biosci , vol.2 , pp. 88-94
    • Osanai, Y.1    Toshima, K.2    Yoshie, N.3    Inoue, Y.4    Matsumura, S.5
  • 21
    • 71749086464 scopus 로고    scopus 로고
    • Removal of 2,4-D, MCPA and Metalaxyl from water using Lewatit VP OC 1163 as sorbent
    • Vergili I, Barlas H. Removal of 2,4-D, MCPA and Metalaxyl from water using Lewatit VP OC 1163 as sorbent. Desalination. 2009; 249: 1107-1114.
    • (2009) Desalination , vol.249 , pp. 1107-1114
    • Vergili, I.1    Barlas, H.2
  • 22
    • 67650353990 scopus 로고    scopus 로고
    • Molecular level structure of (R,S)-3-hydroxybutyrate/(R,S)-3-hydroxy-4-ethoxybutyrate copolyesters with dissimilar architecture
    • Adamus G. Molecular level structure of (R,S)-3-hydroxybutyrate/(R,S)-3-hydroxy-4-ethoxybutyrate copolyesters with dissimilar architecture. Macromolecules. 2009; 42: 4547-4557.
    • (2009) Macromolecules , vol.42 , pp. 4547-4557
    • Adamus, G.1
  • 23
    • 84890885285 scopus 로고    scopus 로고
    • Molecular level structure of novel synthetic analogues of aliphatic biopolyesters as revealed by multistage mass spectrometry
    • PMID: 24370097
    • Adamus G, Kwiecień I, Maksymiak M, Bałakier T, Jurczak J, Kowalczuk M. Molecular level structure of novel synthetic analogues of aliphatic biopolyesters as revealed by multistage mass spectrometry. Anal Chim Acta. 2014; 808: 104-114. doi: 10.1016/j.aca.2013.09.001 PMID: 24370097
    • (2014) Anal Chim Acta , vol.808 , pp. 104-114
    • Adamus, G.1    Kwiecień, I.2    Maksymiak, M.3    Bałakier, T.4    Jurczak, J.5    Kowalczuk, M.6
  • 24
    • 77949492326 scopus 로고    scopus 로고
    • Synthesis and antiproliferative properties of ibuprofen-oligo(3-hydroxybutyrate) conjugates
    • PMID: 20171760
    • Zawidlak-We¸grzyńska B, Kawalec M, Bosek I, Łuczyk-Juzwa M, Adamus G, Rusin A, et al. Synthesis and antiproliferative properties of ibuprofen-oligo(3-hydroxybutyrate) conjugates. Eur J Med Chem. 2010; 45: 1833-1842. doi: 10.1016/j.ejmech.2010.01.020 PMID: 20171760
    • (2010) Eur J Med Chem , vol.45 , pp. 1833-1842
    • Zawidlak-We¸grzyńska, B.1    Kawalec, M.2    Bosek, I.3    Łuczyk-Juzwa, M.4    Adamus, G.5    Rusin, A.6
  • 25
    • 84875154663 scopus 로고    scopus 로고
    • Structural characterization of biocompatible lipoic acid-oligo-(3-hydroxybutyrate) conjugates by electrospray ionization mass spectrometry
    • PMID: 23495024
    • Maksymiak M, Debowska R, Jelonek K, Kowalczuk M, Adamus G. Structural characterization of biocompatible lipoic acid-oligo-(3-hydroxybutyrate) conjugates by electrospray ionization mass spectrometry. Rapid Commun Mass Spectrom. 2013; 27: 773-783. doi: 10.1002/rcm.6509 PMID: 23495024
    • (2013) Rapid Commun Mass Spectrom , vol.27 , pp. 773-783
    • Maksymiak, M.1    Debowska, R.2    Jelonek, K.3    Kowalczuk, M.4    Adamus, G.5
  • 26
    • 84887438871 scopus 로고    scopus 로고
    • Synthesis and structural characterization at the molecular level of oligo(3-hydroxybutyrate) conjugates with antimicrobial agents designed for food packaging materials
    • Kwiecień I, Adamus G, Bartkowiak A, Kowalczuk M. Synthesis and structural characterization at the molecular level of oligo(3-hydroxybutyrate) conjugates with antimicrobial agents designed for food packaging materials. Des Monomers Polym. 2014; 17: 311-321.
    • (2014) Des Monomers Polym , vol.17 , pp. 311-321
    • Kwiecień, I.1    Adamus, G.2    Bartkowiak, A.3    Kowalczuk, M.4
  • 27
    • 84875974865 scopus 로고    scopus 로고
    • Selective reduction of PHA biopolyesters and their synthetic analogues to corresponding PHA oligodiols proved by structural studies
    • PMID: 23464789
    • Kwiecień M, Adamus G, Kowalczuk M. Selective reduction of PHA biopolyesters and their synthetic analogues to corresponding PHA oligodiols proved by structural studies. Biomacromolecules. 2013; 14: 1181-1188. doi: 10.1021/bm400141s PMID: 23464789
    • (2013) Biomacromolecules , vol.14 , pp. 1181-1188
    • Kwiecień, M.1    Adamus, G.2    Kowalczuk, M.3
  • 28
    • 0007042159 scopus 로고
    • Separation and structural characterization of cyclic and open chain oligomers produced in the partial pyrolysis of microbial poly(hydroxybutyrates)
    • Abate R, Ballistreri A, Montaudo G, Giuffrida M, Impallomeni G. Separation and structural characterization of cyclic and open chain oligomers produced in the partial pyrolysis of microbial poly(hydroxybutyrates). Macromolecules. 1995; 28: 7911-7916.
    • (1995) Macromolecules , vol.28 , pp. 7911-7916
    • Abate, R.1    Ballistreri, A.2    Montaudo, G.3    Giuffrida, M.4    Impallomeni, G.5
  • 29
    • 0036406855 scopus 로고    scopus 로고
    • Microbial degradation of polyhydroxyalkanoates
    • PMID: 12213937
    • Jendrossek D, Handrick R. Microbial degradation of polyhydroxyalkanoates. Annu Rev Microbiol. 2002; 56: 403-432. PMID: 12213937
    • (2002) Annu Rev Microbiol , vol.56 , pp. 403-432
    • Jendrossek, D.1    Handrick, R.2
  • 30
    • 84873660418 scopus 로고    scopus 로고
    • Biodegradability of poly(hydroxyalkanoate) materials
    • Numata K, Abe H, Iwata T. Biodegradability of poly(hydroxyalkanoate) materials. Materials. 2009; 2: 1104-1126.
    • (2009) Materials , vol.2 , pp. 1104-1126
    • Numata, K.1    Abe, H.2    Iwata, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.