Department of Biochemistry and Biotechnology, Institute of Biological Sciences, Maria Curie-Skłodowska University, Akademicka 19, 20-033 Lublin, Poland.
Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Via A. Moro 2; 53100 Siena, Italy.
Int J Mol Sci. 2020 Mar 17;21(6):2052. doi: 10.3390/ijms21062052.
Novel sustainable processes involving oxidative enzymatic catalysts are considered as an alternative for classical organic chemistry. The unique physicochemical and bioactive properties of novel bio-products can be obtained using fungal laccase as catalyst. Among them are textile biodyes synthesised during oxidation of substrates belonging to the amine and methoxy organic derivatives. The process of synthesis occurs in mild conditions of pH, temperature, and pressure, and without using harmful oxidants. The effect of fungal laccase activity on the substrates mixture transformation efficiency was analysed in terms of antimicrobial dye synthesis on a large scale. Three new phenazine dyes, obtained in the presence of laccase from , were studied for their structure and properties. The phenazine core structure of the products was a result of tri-molecular transformation of aminomethoxybenzoic acid and aminonaphthalene sulfonic acid isomers. One of the compounds from the synthesised dye, namely 10-((2-carboxy-6-methoxyphenyl)amino)-11-methoxybenzo[a]phenazine-8-carboxylic acid, was able to inhibit the growth of . The high concentration of substrates (5 g/L) was efficiently transformed during 72 h in the mild conditions of pH 4 with the use of laccase with an activity of 200 U per g of the substrates mixture. The new bioactive dye exhibited excellent dyeing properties with concomitant antibacterial and antioxidative activity. The proposed enzyme-mediated synthesis represents an alternative eco-friendly route for the synthesis of novel antimicrobial compounds with high importance for the medical textile industry.
新型可持续的氧化酶催化剂工艺被认为是经典有机化学的替代方法。新型生物产物具有独特的物理化学和生物活性特性,可以使用真菌漆酶作为催化剂获得。其中包括在氧化属于胺和甲氧基有机衍生物的底物时合成的纺织生物染料。该合成过程在 pH、温度和压力的温和条件下进行,且不使用有害氧化剂。分析了真菌漆酶活性对底物混合物转化效率的影响,以大规模合成抗菌染料。在漆酶存在的情况下,从 中获得了三种新的吩嗪染料,并对其结构和性质进行了研究。产物的吩嗪核心结构是氨基甲氧基苯甲酸和氨基萘磺酸异构体的三分子转化的结果。所合成的染料中的一种化合物,即 10-((2-羧基-6-甲氧基苯基)氨基)-11-甲氧基苯并[a]吩嗪-8-羧酸,能够抑制 的生长。在温和条件下(pH 值 4),使用活性为每克底物混合物 200 U 的漆酶,在 72 小时内高效地转化高浓度的底物(5 g/L)。新型生物活性染料表现出优异的染色性能,同时具有抗菌和抗氧化活性。所提出的酶介导合成代表了一种替代的环保方法,用于合成具有医学纺织品行业高度重要性的新型抗菌化合物。