A common active site of polyhydroxyalkanoate synthase from Bacillus cereus YB-4 is involved in polymerization and alcoholysis reactions

Verfasser / Beitragende:
[Manami Hyakutake, Satoshi Tomizawa, Kouhei Mizuno, Tamao Hisano, Hideki Abe, Takeharu Tsuge]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/11(2015-06-01), 4701-4711
Format:
Artikel (online)
ID: 605506507
LEADER caa a22 4500
001 605506507
003 CHVBK
005 20210128100627.0
007 cr unu---uuuuu
008 210128e20150601xx s 000 0 eng
024 7 0 |a 10.1007/s00253-014-6276-4  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-014-6276-4 
245 0 2 |a A common active site of polyhydroxyalkanoate synthase from Bacillus cereus YB-4 is involved in polymerization and alcoholysis reactions  |h [Elektronische Daten]  |c [Manami Hyakutake, Satoshi Tomizawa, Kouhei Mizuno, Tamao Hisano, Hideki Abe, Takeharu Tsuge] 
520 3 |a Polyhydroxyalkanoate (PHA) synthase from Bacillus cereus YB-4 (PhaRCYB4) catalyzes not only PHA polymerization but also alcoholytic cleavage of PHA chains. The alcoholysis activity of PhaRCYB4 is expressed when a hydroxyacyl-CoA monomer is absent but an alcohol compound is present. In this study, we performed alanine mutagenesis of the putative catalytic triad (Cys151, Asp306, and His335) in the PhaCYB4 subunit to identify the active site residues for polymerization and alcoholysis activities. Individual substitution of each triad residue with alanine resulted in loss of both polymerization and alcoholysis activities, suggesting that these residues are commonly shared between polymerization and alcoholysis reactions. The loss of activity was also observed following mutagenesis of the triad to other amino acids, except for one PhaRCYB4 mutant with a C151S substitution, which lost polymerization activity but still possessed cleavage activity towards PHA chains. The low-molecular-weight PHA isolated from the PhaRCYB4(C151S)-expressing strain showed a lower ratio of alcohol capping at the P(3HB) carboxy terminus than did that from the wild-type-expressing strain. This observation implies that hydrolysis activity of PhaRCYB4 might be elicited by the C151S mutation. 
540 |a Springer-Verlag Berlin Heidelberg, 2014 
690 7 |a Bacillus  |2 nationallicence 
690 7 |a Escherichia coli  |2 nationallicence 
690 7 |a Polyhydroxyalkanoate  |2 nationallicence 
690 7 |a Class IV PHA synthase  |2 nationallicence 
690 7 |a Alcoholysis  |2 nationallicence 
690 7 |a Catalytic residue  |2 nationallicence 
700 1 |a Hyakutake  |D Manami  |u Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, 226-8502, Midori-ku, Yokohama, Japan  |4 aut 
700 1 |a Tomizawa  |D Satoshi  |u Department of Biological and Chemical Systems Engineering, Kumamoto National College of Technology, 2627, Hirayamashin-machi, 866-8501, Yatsushiro, Kumamoto, Japan  |4 aut 
700 1 |a Mizuno  |D Kouhei  |u Department of Materials Science and Chemical Engineering, Kitakyushu National College of Technology, 5-20-1 Shii, 802-0985, Kokuraminami-ku, Kitakyushu, Japan  |4 aut 
700 1 |a Hisano  |D Tamao  |u RIKEN SPring-8 Center, 1-1-1 Koto, Sayo-cho, 679-5148, Sayo-gun, Hyogo, Japan  |4 aut 
700 1 |a Abe  |D Hideki  |u Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, 226-8502, Midori-ku, Yokohama, Japan  |4 aut 
700 1 |a Tsuge  |D Takeharu  |u Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, 226-8502, Midori-ku, Yokohama, Japan  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/11(2015-06-01), 4701-4711  |x 0175-7598  |q 99:11<4701  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-014-6276-4  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00253-014-6276-4  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hyakutake  |D Manami  |u Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, 226-8502, Midori-ku, Yokohama, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Tomizawa  |D Satoshi  |u Department of Biological and Chemical Systems Engineering, Kumamoto National College of Technology, 2627, Hirayamashin-machi, 866-8501, Yatsushiro, Kumamoto, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Mizuno  |D Kouhei  |u Department of Materials Science and Chemical Engineering, Kitakyushu National College of Technology, 5-20-1 Shii, 802-0985, Kokuraminami-ku, Kitakyushu, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hisano  |D Tamao  |u RIKEN SPring-8 Center, 1-1-1 Koto, Sayo-cho, 679-5148, Sayo-gun, Hyogo, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Abe  |D Hideki  |u Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, 226-8502, Midori-ku, Yokohama, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Tsuge  |D Takeharu  |u Department of Innovative and Engineered Materials, Tokyo Institute of Technology, 4259 Nagatsuta, 226-8502, Midori-ku, Yokohama, Japan  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/11(2015-06-01), 4701-4711  |x 0175-7598  |q 99:11<4701  |1 2015  |2 99  |o 253