Characterization of hydantoin-5-propionic acid amidohydrolase involved in ergothioneine utilization inBurkholderiasp. HME13

Author:

Muramatsu Hisashi1,Koujitani Akihito2,Yamada Masaaki2,Maguchi Hiroki2,Kashiwagi Takehiro1,Kato Shin-ichiro1

Affiliation:

1. Multidisciplinary Science Cluster, Research and Education Faculty, Kochi University , B200 Monobe, Nankoku , Kochi, Japan

2. Graduate School of Integrated Arts and Sciences, Kochi University , B200 Monobe, Nankoku , Kochi, Japan

Abstract

ABSTRACTIn our previous study, ertABC genes encoding ergothionase, thiourocanate hydratase, and 3-(5-oxo-2-thioxoimidazolidin-4-yl) propionic acid desulfhydrase were identified, all of which may be involved in ergothioneine utilization of Burkholderia sp. HME13. In this study, we identify the ertD gene encoding metal-dependent hydantoin-5-propionic acid amidohydrolase in this strain. Mn2+-containing ErtD showed maximum activity at 45 °C and pH 8.5 and was stable at temperatures up to 45 °C. The Km and Vmax values of Mn2+-containing ErtD for hydantoin-5-propionic acid were 2.8 m m and 16 U/mg, respectively. Real-time polymerase chain reaction (PCR) revealed that ertD expression levels in Burkholderia sp. HME13 cells cultivated in ergothioneine medium were 3.3-fold higher than those in cells cultivated in Luria–Bertani (LB) medium. ErtD activity in the crude extract from Burkholderia sp. HME13 cells cultured in ergothioneine medium was 0.018 U/mg, whereas that in LB medium was not detected. Accordingly, we suggest that ErtD is involved in ergothioneine utilization in this strain.

Publisher

Oxford University Press (OUP)

Subject

Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology

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