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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate](n+1) + CoA
(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
3-hydroxybutyryl-CoA + 3-hydroxyvalerate
poly(3-hydroxybutyrate-co-3-hydroxyvalerate) + CoA
3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
additional information
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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
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(3R)-3-hydroxyacyl-CoA + poly[(R)-3-hydroxyalkanoate]n
CoA + poly[(R)-3-hydroxyalkanoate]n+1
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(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate](n+1) + CoA
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(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate](n+1) + CoA
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(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate](n+1) + CoA
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(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
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(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
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(R)-3-hydroxybutanoyl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxyacyl-CoA + [(R)-3-hydroxyacyl]n
[(R)-3-hydroxyacyl]n+1 + CoA
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3-hydroxybutyryl-CoA + 3-hydroxyvalerate
poly(3-hydroxybutyrate-co-3-hydroxyvalerate) + CoA
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3-hydroxybutyryl-CoA + 3-hydroxyvalerate
poly(3-hydroxybutyrate-co-3-hydroxyvalerate) + CoA
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3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
PhaRCBm synthesizes (R)-3-hydroxybutanoate, P(3HB), with a low-molecular-weight, Mn = 20000
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3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
PhaRCBm synthesizes (R)-3-hydroxybutanoate, P(3HB), with a low-molecular-weight, Mn = 20000
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3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
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3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
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3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
PhaRCBm synthesizes (R)-3-hydroxybutanoate, P(3HB), with a relatively high molecular weight, Mn = 890000
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3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
PhaRCBm synthesizes (R)-3-hydroxybutanoate, P(3HB), with a relatively high molecular weight, Mn = 890000
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3-hydroxybutyryl-CoA + [(R)-3-hydroxybutanoate]n
[(R)-3-hydroxybutanoate]n+1 + CoA
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additional information
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the PhaC from BAcillus cereus also shows a polyhydroxybutanoate hydrolyzing activity, time-dependent change in inverse of degree of polymerization during intracellular P(3HB) degradation at a culture temperature of 37°C, overview
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the PhaC from BAcillus cereus also shows a polyhydroxybutanoate hydrolyzing activity, time-dependent change in inverse of degree of polymerization during intracellular P(3HB) degradation at a culture temperature of 37°C, overview
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the PhaC from BAcillus cereus also shows a polyhydroxybutanoate hydrolyzing activity, time-dependent change in inverse of degree of polymerization during intracellular P(3HB) degradation at a culture temperature of 37°C, overview
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additional information
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the PhaC from BAcillus cereus also shows a polyhydroxybutanoate hydrolyzing activity, time-dependent change in inverse of degree of polymerization during intracellular P(3HB) degradation at a culture temperature of 37°C, overview
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the 3-hydroxyvalerate molar fraction in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) is significantly affected by the type of the precursor used and their respective feeding time
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the 3-hydroxyvalerate molar fraction in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) is significantly affected by the type of the precursor used and their respective feeding time
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I3R9Z3; I3R9Z4
the enzyme is responsible for synthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)
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the enzyme is responsible for synthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)
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the bacteria produce homo-polymer [poly-3-hydroxybutyrate (P3HB)] when only acetate is used as carbon source, and it produces co-polymer [poly-(3-hydroxybutyrate-co-3-hydroxyvalerate) P(3HB-co-3HV)] by addition of co-substrate propionate. Evaluation of PHA production by Pseudomonas pseudoflava strain NBRC-102513 from wastewater containing diverse volatile atty acids (VFA), common products of various wastewaters. Analysis of the PHA spectrum produced from different carbon sources, NMR study, overview
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additional information
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the bacteria produce homo-polymer [poly-3-hydroxybutyrate (P3HB)] when only acetate is used as carbon source, and it produces co-polymer [poly-(3-hydroxybutyrate-co-3-hydroxyvalerate) P(3HB-co-3HV)] by addition of co-substrate propionate. Evaluation of PHA production by Pseudomonas pseudoflava strain NBRC-102513 from wastewater containing diverse volatile fatty acids (VFA), common products of various wastewaters. Analysis of the PHA spectrum produced from different carbon sources, NMR study, overview. MW and polydispersity index (PDI, Mw/Mn) of the P3HB produced by Pseudomonas pseudoflava is 17.63 kDa and 3.3 respectively. MW and PDI of the co-polymer P(3HB-co-3HV) produced by Pseudomonas pseudoflava is 52.33 kDa and 5.7 respectively. The Mw of the standard P(3HB-co-3HV) is 110 kDa, and PDI is 4.3. Pseudomonas pseudoflava can produce biopolymers with relatively lower dispersity
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additional information
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the bacteria produce homo-polymer [poly-3-hydroxybutyrate (P3HB)] when only acetate is used as carbon source, and it produces co-polymer [poly-(3-hydroxybutyrate-co-3-hydroxyvalerate) P(3HB-co-3HV)] by addition of co-substrate propionate. Evaluation of PHA production by Pseudomonas pseudoflava strain NBRC-102513 from wastewater containing diverse volatile fatty acids (VFA), common products of various wastewaters. Analysis of the PHA spectrum produced from different carbon sources, NMR study, overview. MW and polydispersity index (PDI, Mw/Mn) of the P3HB produced by Pseudomonas pseudoflava is 17.63 kDa and 3.3 respectively. MW and PDI of the co-polymer P(3HB-co-3HV) produced by Pseudomonas pseudoflava is 52.33 kDa and 5.7 respectively. The Mw of the standard P(3HB-co-3HV) is 110 kDa, and PDI is 4.3. Pseudomonas pseudoflava can produce biopolymers with relatively lower dispersity
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additional information
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the bacteria produce homo-polymer [poly-3-hydroxybutyrate (P3HB)] when only acetate is used as carbon source, and it produces co-polymer [poly-(3-hydroxybutyrate-co-3-hydroxyvalerate) P(3HB-co-3HV)] by addition of co-substrate propionate. Evaluation of PHA production by Pseudomonas pseudoflava strain NBRC-102513 from wastewater containing diverse volatile fatty acids (VFA), common products of various wastewaters. Analysis of the PHA spectrum produced from different carbon sources, NMR study, overview. MW and polydispersity index (PDI, Mw/Mn) of the P3HB produced by Pseudomonas pseudoflava is 17.63 kDa and 3.3 respectively. MW and PDI of the co-polymer P(3HB-co-3HV) produced by Pseudomonas pseudoflava is 52.33 kDa and 5.7 respectively. The Mw of the standard P(3HB-co-3HV) is 110 kDa, and PDI is 4.3. Pseudomonas pseudoflava can produce biopolymers with relatively lower dispersity
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additional information
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the bacteria produce homo-polymer [poly-3-hydroxybutyrate (P3HB)] when only acetate is used as carbon source, and it produces co-polymer [poly-(3-hydroxybutyrate-co-3-hydroxyvalerate) P(3HB-co-3HV)] by addition of co-substrate propionate. Evaluation of PHA production by Pseudomonas pseudoflava strain NBRC-102513 from wastewater containing diverse volatile fatty acids (VFA), common products of various wastewaters. Analysis of the PHA spectrum produced from different carbon sources, NMR study, overview. MW and polydispersity index (PDI, Mw/Mn) of the P3HB produced by Pseudomonas pseudoflava is 17.63 kDa and 3.3 respectively. MW and PDI of the co-polymer P(3HB-co-3HV) produced by Pseudomonas pseudoflava is 52.33 kDa and 5.7 respectively. The Mw of the standard P(3HB-co-3HV) is 110 kDa, and PDI is 4.3. Pseudomonas pseudoflava can produce biopolymers with relatively lower dispersity
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Class II PhaC synthesize mcl-PHAs based on the alkane (C6 to C14) precursors
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Class II PhaC synthesize mcl-PHAs based on the alkane (C6 to C14) precursors
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additional information
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Class II PhaC synthesize mcl-PHAs based on the alkane (C6 to C14) precursors
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additional information
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Class II PhaC synthesize mcl-PHAs based on the alkane (C6 to C14) precursors
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additional information
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Class II PhaC synthesize mcl-PHAs based on the alkane (C6 to C14) precursors
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recombinant enzyme, expressed in phaC-deficient Cupriavidus necator, is able to accumulate PHA homopolymers and copolymers including poly(3-hydroxybutyrate) [P(3HB)], poly(3-hydroxybutyrate-co-3-hydroxyvalerate) [P(3HB-co-3HV)], poly(3-hydroxybutyrate-co-5-hydroxyvalerate) [P(3HB-co-5HV)], poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3HB-co-4HB)], poly(3-hydroxybutyrate-co-3-hydroxy-4-methylvalerate) [P(3HB-co-3H4MV)], and poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) [P(3HB-co-3HHx)], when suitable precursors are provided
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