Lysozyme from chicken egg white
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Lysozyme from chicken egg white

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

It's a bactericidal enzyme found in eggs that lyses gram-positive bacteria.

Category
Functional Peptides
Catalog number
BAT-010524
CAS number
12650-88-3
Molecular Formula
C99H159N37O23
Molecular Weight
2235.6
IUPAC Name
2-[[4-amino-2-[[2-[[2-[2-[[2-[[2-[2-[[2-[[2-[[2-[[5-amino-2-[[1-[2-[[2-[[2-[[2-[(2-amino-5-carbamimidamidopentanoyl)amino]-3-methylbutanoyl]amino]-3-methylbutanoyl]amino]-5-carbamimidamidopentanoyl]amino]-3-carboxypropanoyl]pyrrolidine-2-carbonyl]amino]-5-oxopentanoyl]amino]acetyl]amino]-3-methylpentanoyl]amino]-5-carbamimidamidopentanoyl]amino]propanoylamino]-3-(1H-indol-3-yl)propanoyl]amino]-3-methylbutanoyl]amino]propanoylamino]-3-(1H-indol-3-yl)propanoyl]amino]-5-carbamimidamidopentanoyl]amino]-4-oxobutanoyl]amino]-5-carbamimidamidopentanoic acid
Synonyms
Mucopeptide N-acetylmuramoylhydrolase; Muramidase
Appearance
White Lyophilized Powder
Purity
>98%
Storage
Store at -20°C
Solubility
Soluble in Water
InChI
InChI=1S/C99H159N37O23/c1-11-50(8)77(132-72(139)46-120-81(145)63(32-33-70(101)137)124-88(152)69-31-21-39-136(69)93(157)68(43-73(140)141)131-84(148)62(29-19-37-116-98(109)110)125-90(154)75(48(4)5)135-91(155)76(49(6)7)133-80(144)57(100)24-16-34-113-95(103)104)92(156)126-60(27-17-35-114-96(105)106)82(146)121-51(9)78(142)129-66(41-54-45-119-59-26-15-13-23-56(54)59)87(151)134-74(47(2)3)89(153)122-52(10)79(143)128-65(40-53-44-118-58-25-14-12-22-55(53)58)85(149)123-61(28-18-36-115-97(107)108)83(147)130-67(42-71(102)138)86(150)127-64(94(158)159)30-20-38-117-99(111)112/h12-15,22-23,25-26,44-45,47-52,57,60-69,74-77,118-119H,11,16-21,24,27-43,46,100H2,1-10H3,(H2,101,137)(H2,102,138)(H,120,145)(H,121,146)(H,122,153)(H,123,149)(H,124,152)(H,125,154)(H,126,156)(H,127,150)(H,128,143)(H,129,142)(H,130,147)(H,131,148)(H,132,139)(H,133,144)(H,134,151)(H,135,155)(H,140,141)(H,158,159)(H4,103,104,113)(H4,105,106,114)(H4,107,108,115)(H4,109,110,116)(H4,111,112,117)
InChI Key
ZJCXKXFAOCLSRV-UHFFFAOYSA-N
Canonical SMILES
CCC(C)C(C(=O)NC(CCCNC(=N)N)C(=O)NC(C)C(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)NC(C(C)C)C(=O)NC(C)C(=O)NC(CC3=CNC4=CC=CC=C43)C(=O)NC(CCCNC(=N)N)C(=O)NC(CC(=O)N)C(=O)NC(CCCNC(=N)N)C(=O)O)NC(=O)CNC(=O)C(CCC(=O)N)NC(=O)C5CCCN5C(=O)C(CC(=O)O)NC(=O)C(CCCNC(=N)N)NC(=O)C(C(C)C)NC(=O)C(C(C)C)NC(=O)C(CCCNC(=N)N)N
1.Construction of antibacterial poly(ethylene terephthalate) films via layer by layer assembly of chitosan and hyaluronic acid.
Del Hoyo-Gallego S1, Pérez-Álvarez L2, Gómez-Galván F1, Lizundia E1, Kuritka I3, Sedlarik V3, Laza JM1, Vila-Vilela JL1. Carbohydr Polym. 2016 Jun 5;143:35-43. doi: 10.1016/j.carbpol.2016.02.008. Epub 2016 Feb 4.
Polyelectrolytic multilayers (PEMs) with enhanced antibacterial properties were built up onto commercial poly(ethylene terephthalate) (PET) films based on the layer by layer assembling of bacterial contact killing chitosan and bacterial repelling highly hydrated hyaluronic acid. The optimization of the aminolysis modification reaction of PET was carried out by the study of the mechanical properties and the surface characterization of the modified polymers. The layer by layer assembly was successfully monitored by TEM microscopy, surface zeta-potential, contact angle measurements and, after labeling with fluorescein isothiocyanate (FTIC) by absorption spectroscopy and confocal fluorescent microscopy. Beside, the stability of the PEMs was studied at physiological conditions in absence and in the presence of lysozyme and hyaluronidase enzymes. Antibacterial properties of the obtained PEMs against Escherichia coli were compared with original commercial PET.
2.Structure, morphology and properties of genipin-crosslinked carboxymethylchitosan porous membranes.
Fiamingo A1, Campana-Filho SP2. Carbohydr Polym. 2016 Jun 5;143:155-63. doi: 10.1016/j.carbpol.2016.02.016. Epub 2016 Feb 8.
Highly porous genipin cross-linked membranes of carboxymethylchitosan exhibiting different crosslinking degree (3%<CrD¯ < 18%) were produced by using different concentrations of genipin and carboxymethylchitosan possessing high, medium or low molecular weight. The membranes were able to adsorb high amounts of PBS and presented high ultimate tensile strength and elongation-at-break the lower the crosslinking degree and the higher the molecular of the parent carboxymethylchitosan. Particularly, the membrane prepared from high molecular weight carboxymethylchitosan displayed higher swelling ratio (17.5g/g), ultimate tensile strength (≥300kPa) and elongation-at-break (≥65%). The susceptibility to lysozyme degradation depends only on the crosslinking degree of the membranes, the degradation rate being faster the lower the crosslinking degree. The preparation of lightly genipin cross-linked carboxymethylchitosan membranes displaying appropriated properties to fulfill specific applications as biomaterials is envisaged by using high molecular weight carboxymethylchitosan.
3.An aerogel obtained from chemo-enzymatically oxidized fenugreek galactomannans as a versatile delivery system.
Rossi B1, Campia P2, Merlini L3, Brasca M4, Pastori N5, Farris S6, Melone L7, Punta C8, Galante YM9. Carbohydr Polym. 2016 Jun 25;144:353-61. doi: 10.1016/j.carbpol.2016.02.007. Epub 2016 Feb 26.
We describe a new aerogel obtained from laccase-oxidized galactomannans of the leguminous plant fenugreek (Trigonella foenum-graecum) and suggest its potential practical use. Laccase/TEMPO oxidation of fenugreek in aqueous solution caused a viscosity increase of over 15-fold. A structured, elastic, stable hydrogel was generated, due to formation of carbonyl groups from primary OH of galactose side units and subsequent establishment of hemiacetalic bonds with available free hydroxyl groups. Upon lyophilization of this hydrogel, a water-insoluble aerogel was obtained (EOLFG), capable of uptaking aqueous or organic solvents over 20 times its own weight. The material was characterized by scanning electron microscopy, FT-IR, elemental analysis and (13)C CP-MAS NMR spectroscopy and its mechanical properties were investigated. To test the EOLFG as a delivery system, the anti-microbial enzyme lysozyme was used as model active principle. Lysozyme was added before or after formation of the aerogel, entrapped or absorbed in the gel, retained and released in active form, as proven by its hydrolytic glycosidase activity on lyophilized Micrococcus lysodeikticus cells wall peptidoglycans.
4.Effects of Dietary n-3 Highly Unsaturated Fatty Acids (HUFAs) on Growth, Fatty acid Profiles, Antioxidant Capacity and Immunity of Sea Cucumber Apostichopus japonicus (Selenka).
Yu H1, Gao Q2, Dong S3, Zhou J4, Ye Z5, Lan Y6. Fish Shellfish Immunol. 2016 Apr 11. pii: S1050-4648(16)30164-4. doi: 10.1016/j.fsi.2016.04.013. [Epub ahead of print]
The present study was conducted to understand the effects of dietary n-3 highly unsaturated fatty acids (HUFAs) on growth, fatty acid profiles, antioxidant capacity and the immunity of sea cucumber Apostichopus japonicus (Selenka). Five experimental diets were prepared, containing graded levels of n-3 HUFAs (0.46%, 0.85%, 1.25%, 1.61% and 1.95%, respectively), and the 0.46% group was used as control group. The specific growth rates, fatty acid profiles, activities and gene expression of antioxidative enzymes and lysozyme of the sea cucumbers that were fed with the 5 experimental diets were determined. The results showed that the specific growth rate of sea cucumbers in all the treatment groups significantly increased compared to the control group (P < 0.05), indicating the positive effects of n-3 HUFAs on the growth of sea cucumbers. The contents of eicosapentaenoic acid (EPA; 20:5n-3) and docosahexaenoic acid (DHA; 22:6n-3) in the body wall of the sea cucumbers gradually increased with the increasing levels of n-3 HUFAs in the diets.
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