Pozdnyakova Natalia N, Babicheva Tatiana S, Chernova Daria S, Sungurtseva Irina Yu, Zakharevich Andrey M, Shmakov Sergei L, Shipovskaya Anna B
Institute of Chemistry, Saratov National Research State University named after N.G. Chernyshevsky, 83 Astrakhanskaya St., Saratov 410012, Russia.
Institute of Biochemistry and Physiology of Plants and Microorganisms, Saratov Scientific Centre of the Russian Academy of Sciences (IBPPM RAS), 13 Entuziastov Prosp., Saratov 410049, Russia.
J Fungi (Basel). 2025 Jul 29;11(8):565. doi: 10.3390/jof11080565.
The majority of studies of fungal utilization of chitosan are associated with the production of a specific enzyme, chitosanase, which catalyzes the hydrolytic cleavage of the macrochain. In our opinion, the development of approaches to obtaining materials with new functional properties based on non-destructive chitosan transformation by living organisms and their enzyme systems is promising. This study was conducted using a wide range of classical and modern methods of microbiology, biochemistry, and physical chemistry. The ability of the ascomycete Schltdl. to modify films of chitosan with average-viscosity molecular weights of 200, 450, and 530 kDa was discovered. was shown to use chitosan as the sole source of carbon/energy and actively overgrew films without deformations and signs of integrity loss. Scanning electron microscopy (SEM) recorded an increase in the porosity of film substrates. An analysis of the FTIR spectra revealed the occurrence of oxidation processes and crosslinking of macrochains without breaking -(1,4)-glycosidic bonds. After growth, the resistance of the films to mechanical dispersion and the degree of ordering of the polymer structure increased, while their solubility in the acetate buffer with pH 4.4 and sorption capacity for Fe and Cu decreased. Elemental analysis revealed a decrease in the nitrogen content in chitosan, which may indicate its inclusion into the fungal metabolism. The film transformation was accompanied by the production of extracellular hydrolase (different from chitosanase) and peroxidase, as well as biosurfactants. The results obtained indicate a specific mechanism of aminopolysaccharide transformation by . Although the biochemical mechanisms of action remain to be analyzed in detail, the results obtained create new ways of using fungi and show the potential for the use of and/or its extracellular enzymes for the formation of chitosan-containing materials with the required range of functional properties and qualities for biotechnological applications.
大多数关于真菌利用壳聚糖的研究都与一种特定酶——壳聚糖酶的产生有关,该酶催化大分子链的水解裂解。在我们看来,基于生物体及其酶系统对壳聚糖进行无损转化来获得具有新功能特性材料的方法的开发是很有前景的。本研究采用了广泛的经典和现代微生物学、生物化学及物理化学方法。发现子囊菌Schltdl.能够修饰平均粘度分子量分别为200 kDa、450 kDa和530 kDa的壳聚糖膜。结果表明该菌能将壳聚糖作为唯一的碳/能量来源,并能在不发生变形和完整性损失迹象的情况下积极地在膜上过度生长。扫描电子显微镜(SEM)记录到膜基质的孔隙率增加。傅里叶变换红外光谱(FTIR)分析表明发生了氧化过程以及大分子链的交联,而-(1,4)-糖苷键未断裂。生长后,膜对机械分散的抗性以及聚合物结构的有序度增加,而它们在pH 4.4的醋酸盐缓冲液中的溶解度以及对铁和铜的吸附能力下降。元素分析表明壳聚糖中的氮含量降低,这可能表明其被纳入了真菌的代谢过程。膜的转化伴随着细胞外水解酶(不同于壳聚糖酶)、过氧化物酶以及生物表面活性剂的产生。所获得的结果表明了Schltdl.转化氨基多糖的特定机制。尽管其生化作用机制仍有待详细分析,但所获得的结果开创了利用真菌的新途径,并显示出利用Schltdl.和/或其细胞外酶来形成具有生物技术应用所需功能特性和质量范围的含壳聚糖材料的潜力。