Abstract:Here we describe a stoichiometric ion-complex of archaeal poly-γ-L-glutamate (L-PGA) and hexadecylpyridinium cation (HDP(+)), called PGAIC, which shows remarkable chemical resistance and potential as a novel functional thermoplastic. PGAIC films suppressed the proliferation of prokaryotic (Escherichia coli, Bacillus subtilis, Salmonella typhimurium, and Staphylococcus aureus) and eukaryotic (Saccharomyces cerevisiae) microorganisms. Moreover, its antifungal activity was demonstrated against a prevalent species… Show more
“…Although PGAIC is an ionic complex, it was unexpectedly stable to chemicals such as salts, acids and alkalis, suggesting the involvement of a driving force in the solidification of PGAIC other than a typical ionic interaction. It is noteworthy that PGAIC exhibits good solubility in alcohols (Ashiuchi et al ., 2013a), whereas PGA itself never dissolves in alcohols. These transformable properties must be taken into account when processing PGA for diverse applications.…”
Section: Chemical Transformationmentioning
confidence: 99%
“…Ashiuchi and colleagues (2013a) recently demonstrated that a compound used in toothpaste, called hexadecylpyridinium cation (HDP + ), serves as a potent candidate to suppress the extreme hydrophilicity of PGA. In fact, a water-insoluble complex was readily formed by mixing PGA and HDP + at 60°C for 30 min.…”
Poly-γ-glutamate (PGA), a novel polyamide material with industrial applications, possesses a nylon-like backbone, is structurally similar to polyacrylic acid, is biodegradable and is safe for human consumption. PGA is frequently found in the mucilage of natto, a Japanese traditional fermented food. To date, three different types of PGA, namely a homo polymer of d-glutamate (D-PGA), a homo polymer of l-glutamate (L-PGA), and a random copolymer consisting of d- and l-glutamate (DL-PGA), are known. This review will detail the occurrence and physiology of PGA. The proposed reaction mechanism of PGA synthesis including its localization and the structure of the involved enzyme, PGA synthetase, are described. The occurrence of multiple carboxyl residues in PGA likely plays a role in its relative unsuitability for the development of bio-nylon plastics and thus, establishment of an efficient PGA-reforming strategy is of great importance. Aside from the potential applications of PGA proposed to date, a new technique for chemical transformation of PGA is also discussed. Finally, some techniques for PGA and its derivatives in advanced material technology are presented.
“…Although PGAIC is an ionic complex, it was unexpectedly stable to chemicals such as salts, acids and alkalis, suggesting the involvement of a driving force in the solidification of PGAIC other than a typical ionic interaction. It is noteworthy that PGAIC exhibits good solubility in alcohols (Ashiuchi et al ., 2013a), whereas PGA itself never dissolves in alcohols. These transformable properties must be taken into account when processing PGA for diverse applications.…”
Section: Chemical Transformationmentioning
confidence: 99%
“…Ashiuchi and colleagues (2013a) recently demonstrated that a compound used in toothpaste, called hexadecylpyridinium cation (HDP + ), serves as a potent candidate to suppress the extreme hydrophilicity of PGA. In fact, a water-insoluble complex was readily formed by mixing PGA and HDP + at 60°C for 30 min.…”
Poly-γ-glutamate (PGA), a novel polyamide material with industrial applications, possesses a nylon-like backbone, is structurally similar to polyacrylic acid, is biodegradable and is safe for human consumption. PGA is frequently found in the mucilage of natto, a Japanese traditional fermented food. To date, three different types of PGA, namely a homo polymer of d-glutamate (D-PGA), a homo polymer of l-glutamate (L-PGA), and a random copolymer consisting of d- and l-glutamate (DL-PGA), are known. This review will detail the occurrence and physiology of PGA. The proposed reaction mechanism of PGA synthesis including its localization and the structure of the involved enzyme, PGA synthetase, are described. The occurrence of multiple carboxyl residues in PGA likely plays a role in its relative unsuitability for the development of bio-nylon plastics and thus, establishment of an efficient PGA-reforming strategy is of great importance. Aside from the potential applications of PGA proposed to date, a new technique for chemical transformation of PGA is also discussed. Finally, some techniques for PGA and its derivatives in advanced material technology are presented.
“…In the archaeal domain, toxin-antitoxin system genes have been identified in Thermoplasmatales, several methanotrophs, and in the symbiotic archaeon, Nanoarchaeum equitans [64,65]. One study also mentions the use of a stoichiometric ion-complex of archaeal poly-g-Lglutamate and hexadecylpyridinium cation, called PGAIC, which showed antimicrobial activity against several bacterial and eukaryotic microorganisms, and was suggested for use as an antimicrobial coating agent [66].…”
“…Hexadecylpyridinium chloride (HDP) that includes a quaternary ammonium cation (Figure 1) is known as a disinfectant (Johansen et al, 2006). Quaternary ammonium cation binds to the carboxylic acid group of γ-PGA via an ionic bond, and water-insoluble and antimicrobial complexes are thus formed (Ashiuchi et al, 2013;Ashiuchi et al, 2015). Therefore, we hypothesized that it is possible to purify γ-PGA from the culture broth using the water-insoluble complex.…”
Poly-gamma-glutamic acid (γ-PGA) is a water-soluble, nontoxic biodegradable polymer. It is extensively utilized in medicines, foodstu s, and cosmetics, as well as in water treatment. Highly pure γ-PGA is required for various purposes. In many cases, γ-PGA is produced by microbes of Bacillus sp. However, an increase in the viscosity of the culture broth is one of the major problems of γ-PGA production, as higher viscosity makes the separation and puri cation steps di cult. Herein, we propose a novel method to obtain pure γ-PGA using gemini quaternary ammonium salts (GQASs). The quaternary ammonium cation of GQASs binds to the carboxylic acid group of γ-PGA via an ionic bond, following which waterinsoluble and antimicrobial complexes are formed. These complexes are obtained in the aqueous solution, which were resolved in ethanol solution. With an increase in the added amount of GQAS, the negative charge of the complex decreased in the aqueous solution. Subsequently, the GQAS within the complexes was dissociated by the addition of NaCl, a ording pure γ-PGA in a high yield. Moreover, the complexes were shown to have antibacterial activity and adhered to glass, indicating that the complex itself has a utility value.
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