Polylysine
 | |
| Names | |
|---|---|
| IUPAC name
Poly[imino[(2S)-2-amino-1-oxo-1,6-hexanediyl | |
| Identifiers | |
25104-18-1  | |
| Properties | |
| (C6H12N2O)n | |
| Molar mass | variable 4700 g/mol (degree of polymerization = 30) |
| Melting point | 142.2 °C (288.0 °F; 415.3 K) |
| Soluble | |
| Basicity (pKb) | 5 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Polylysine refers to several types of lysine homopolymers, which may differ from each other in terms of stereochemistry and link position.
Chemical structure and function
The precursor amino acid lysine contains two amino groups, one at the α-carbon and one at the ε-carbon. Either can be the location of polymerization, resulting in α-polylysine or ε-polylysine. Polylysine is a homopolypeptide belonging to the group of cationic polymers: at pH 7, polylysine contains a positively charged hydrophilic amino group.
α-Polylysine is a synthetic polymer, which can be composed of either L-lysine or D-lysine. "L" and "D" refer to the chirality at lysine's central carbon. This results in poly-L-lysine (PLL) and poly-D-lysine (PDL) respectively.[1]
ε-Polylysine (ε-poly-L-lysine, EPL) is typically produced as a homopolypeptide of approximately 25–30 L-lysine residues.[2] According to research, ε-polylysine is adsorbed electrostatically to the cell surface of the bacteria, followed by a stripping of the outer membrane. This eventually leads to the abnormal distribution of the cytoplasm causing damage to the bacterial cell[3] that is produced by bacterial fermentation. ε-Poly-L-lysine is used as a natural preservative in food products.
Production
Production of polylysine by natural fermentation is only observed in strains of bacteria in the genus Streptomyces. Streptomyces albulus is most often used in scientific studies and is also used for the commercial production of ε-polylysine.
α-Polylysine is synthetically produced by a basic polycondensation reaction.[4]
History
The production of ε-polylysine by natural fermentation was first described by researchers Shoji Shima and Heiichi Sakai in 1977.[2] Since the late 1980s, polylysine has been approved by the Japanese Ministry of Health, Labour and Welfare as a preservative in food. In January 2004, polylysine became generally recognized as safe (GRAS) certified in the United States.[5]
Polylysine in food
ε-Polylysine is used commercially as a food preservative in Japan, Korea and in imported items sold in the United States. Food products containing polylysine are mainly found in Japan. The use of polylysine is common in food applications such as boiled rice, cooked vegetables, soups, noodles and sliced fish (sushi).[6]
Literature studies have reported an antimicrobial effect of ε-polylysine against yeast, fungi, Gram-positive bacteria and Gram-negative bacteria.[7]
Polylysine has a light yellow appearance and is slightly bitter in taste whether in powder or liquid form.
Polylysine in tissue culture
α-Polylysine is commonly used to coat tissue cultureware as an attachment factor which improves cell adherence. This phenomenon is based on the interaction between the positively charged polymer and negatively charged cells or proteins. While the poly-L-lysine (PLL) precursor amino acid occurs naturally, the poly-D-lysine (PDL) precursor is an artificial product. The latter is therefore thought to be resistant to enzymatic degradation and so may prolong cell adherence.[8]
Chemical modification
In 2010, hydrophobically modified ε-polylysine was synthesized by reacting EPL with octenyl succinic anhydride (OSA).[9] It was found that OSA-g-EPLs had glass transition temperatures lower than EPL. They were able to form polymer micelles in water and to lower the surface tension of water, confirming their amphiphilic properties. The antimicrobial activities of OSA-g-EPLs were also examined, and the minimum inhibitory concentrations of OSA-g-EPLs against Escherichia coli O157:H7 remained the same as that of EPL. Therefore, modified EPLs have the potential of becoming bifunctional molecules, which can be used either as surfactants or emulsifiers in the encapsulation of water-insoluble drugs or as antimicrobial agents.
References
- ↑ Sitterley, G. (2008). Poly-l-lysine cell attachment protocol. BioFiles, 3(8), 12.
- 1 2 Shima, S. and Sakai H. (1977). "Polylysine produced by Streptomyces". Agricultural and Biological Chemistry 41: 1807–1809. doi:10.1271/bbb1961.41.1807.
- ↑ Shima, S.; et al. (1984). "Antimicrobial action of ε-poly-L-lysine". Journal of Antibiotics 37 (11): 1449–1455. doi:10.7164/antibiotics.37.1449. PMID 6392269.
- ↑
- ↑ GRAS Notice No. GRN 000135
- ↑ Hiraki, J.; et al. (2003). "Use of ADME studies to confirm the safety of ε-polylysine as a preservative in food". Regulatory Toxicology and Pharmacology 37 (2): 328–340. doi:10.1016/S0273-2300(03)00029-1. PMID 12726761.
- ↑ Hiraki, J. (1995). "Basic and applied studies on ε-polylysine". Journal of Antibacterial Antifungal Agents 23: 349–354.
- ↑ Mazia, D.; et al. (1975). "Adhesion of cells to surfaces coated with polylysine. Applications to electron microscopy.". The Journal of Cell Biology 66 (1): 198–200. doi:10.1083/jcb.66.1.198. PMC 2109515. PMID 1095595.
- ↑ Yu, et al, J. Agri Food Chem, 2010 Jan 27;58(2):1290-5.