Engineering of class I lactate-polymerizing polyhydroxyalkanoate synthases from Ralstonia eutropha that synthesize lactate-based polyester with a block nature
Class I polyhydroxyalkanoate (PHA) synthase from Ralstonia eutropha (PhaC Re ) was engineered so as to acquire an unusual lactate (LA)-polymerizing activity. To achieve this, the site-directed saturation mutagenesis of PhaC Re was conducted at position 510, which corresponds to position 481 in the i...
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Veröffentlicht in: | Applied microbiology and biotechnology 2013-04, Vol.97 (8), p.3441-3447 |
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Sprache: | eng |
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Zusammenfassung: | Class I polyhydroxyalkanoate (PHA) synthase from
Ralstonia eutropha
(PhaC
Re
) was engineered so as to acquire an unusual lactate (LA)-polymerizing activity. To achieve this, the site-directed saturation mutagenesis of PhaC
Re
was conducted at position 510, which corresponds to position 481 in the initially discovered class II LA-polymerizing PHA synthase (PhaC1
Ps
STQK), a mutation in which (Gln481Lys) was shown to be essential to its LA-polymerizing activity (Taguchi et al., Proc Natl Acad Sci USA 105(45):17323–17327,
2008
). The LA-polymerizing activity of the PhaC
Re
A510X mutants was evaluated based on the incorporation of LA units into the P[3-hydroxybutyrate(3HB)] backbone in vivo using recombinant
Escherichia coli
LS5218. Among 19 PhaC
Re
(A510X) mutants, 15 synthesized P (LA-
co
-3HB), indicating that the 510 residue plays a critical role in LA polymerization. The polymer synthesized by PhaC
Re
A510S was fractionated using gel permeation chromatography in order to remove the low molecular weight fractions. The
13
C and
1
H NMR analyses of the high molecular weight fraction revealed that the polymer was a P(7 mol% LA-
co
-3HB) copolymer with a weight-averaged molecular weight of 3.2 × 10
5
Da. Interestingly, the polymer contained an unexpectedly high ratio of an LA-LA*-LA triad sequence, suggesting that the polymer synthesized by PhaC
Re
mutant may not be a random copolymer, but presumably had a block sequence. |
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ISSN: | 0175-7598 1432-0614 |
DOI: | 10.1007/s00253-012-4231-9 |