Publications by authors named "W Hakamata"

The first steps in chitin degradation in marine bacteria involve chitinase, which produces N,N'-diacetylchitobiose (GlcNAc)2 from chitin. Moreover, in Vibrio bacteria, chitinase activity is enhanced by heterodisaccharide β-N-acetyl-d-glucosaminyl-(1,4)-d-glucosamine (GlcNAc-GlcN) produced from (GlcNAc)2 by chitin oligosaccharide deacetylase (COD). However, the role of COD in other marine bacteria, such as Shewanella, remains unexplored.

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Bifidobacterium pseudocatenulatum grows well in the early stages of cultivation in medium containing sucrose (Suc), whereas its growth in medium containing the analogue disaccharide N-acetylsucrosamine (SucNAc) tends to exhibit a considerable delay. To elucidate the cause of this phenomenon, we investigated the proliferation pattern of B. pseudocatenulatum in medium containing D-glucose (Glc) and SucNAc and identified the enzyme that degrades this disaccharide.

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Utilizing transglycosylation reaction catalyzed by β- -acetylhexosaminidase of , β-D-fructofuranosyl-(2↔1)-α- , ´diacetylchitobioside (GlcNAc -Fru) was synthesized from -acetylsucrosamine and , ´-diacetylchitobiose (GlcNAc ), and β-D-fructofuranosyl-(2↔1)-α- , ´, ´´-triacetylchitotrioside (GlcNAc -Fru) was synthesized from GlcNAc -Fru and GlcNAc . Through purification by charcoal column chromatography, pure GlcNAc -Fru and GlcNAc -Fru were obtained in molar yields of 33.0 % and 11.

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Serum albumin (SA), the most abundant protein in circulation, functions as a carrier protein, osmoregulator, and antioxidant. Generally, SA exerts its antioxidative effects by scavenging reactive oxygen species. Because marine mammals are superior divers, they are intermittently exposed to oxidative stress induced by rapid reperfusion of oxygen to ischemic tissues after the dive.

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Article Synopsis
  • The GLB1 and GALC genes produce enzymes important for human lysosomes, with GLB1 involved in aging cell detection and GALC linked to Krabbe disease.
  • A new method to find inhibitors of a previously unidentified Golgi β-galactosidase involved high-throughput screening, leading to the discovery of a potent compound called ARM07.
  • ARM07 showed strong inhibition of β-galactosidase activity and may be useful for research on lysosomal storage diseases and aging cell functions.
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