季铵盐磷酸化衍生物:合成、x射线晶体结构、抗菌活性和生态毒性。

IF 2.6 3区 生物学 Q3 MICROBIOLOGY
Rustam R Davletshin, Polina A Kuryntseva, Aidar M Gayneev, Gulnaz Sh Galieva, Svetlana Yu Selivanovskaya, Natal'ya V Davletshina, Kamil A Ivshin, Daut R Islamov
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引用次数: 0

摘要

合成了苯扎氯铵-二异丙氧磷基甲烷(二甲基十二烷基铵)溴化1(磷酸化季铵盐)和异丙氧磷基甲烷(二甲基烷基铵)2(磷酸化甜菜碱)的磷酸化结构类似物。化合物1的结构通过单晶x射线衍射研究得到了证实。对合成的化合物对水生生物和开花植物进行了抗菌、抗真菌和生态毒理学评价。两种化合物对尾尾草履虫(Protista)和尾尾Ceriodaphnia affinis (Cladocera)的毒性相当,化合物1-0.62 g/L (P. caudatum)、0.13 g/L (C. affinis)和化合物2-0.90 g/L (P. caudatum)、0.08 g/L (C. affinis)的EC10值均相当。这些值表明,与对照苯扎氯铵(BC)相比,毒力显著降低(尾螺EC10 = 110 μg/L,亲和螺EC10 = 30 μg/L)。这两种化合物对普通小球藻都没有毒性,而BC对小球藻的生长有93%的抑制作用。然而,化合物1和2在10.0 g/L浓度下对莴苣种子萌发均有抑制作用,而BC在10 g/L浓度下仅表现出微弱的植物毒性。圆盘扩散法测定化合物1对枯草芽孢杆菌(革兰氏阳性)、荧光假单胞菌(革兰氏阴性)和镰刀菌(镰刀菌)均有较好的抑菌活性。化合物2在10.0 g/L时仅对枯草芽孢杆菌和镰刀菌有活性。在所有三种微生物中,化合物1比BC更有效地抑制微生物生长,而化合物2的性能与对照组没有显著差异。因此,合成的化合物1显示出与参比化合物(Miramistin, Benzalkonium Chloride)相当的抗菌功效,同时显示出明显较低的生态毒性。这种增强的安全性表明,它的生产和应用将降低环境风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phosphorylated Derivatives of Quaternary Ammonium Salts: Synthesis, X-Ray Crystal Structure, Antimicrobial Activity and Ecotoxicity.

Phosphorylated structural analogs of Benzalkonium Chloride-diisopropoxyphosphorylmethane (dimethyldodecylammonium) bromide 1 (phosphorylated quaternary ammonium salt) and isopropoxyphosphorylmethane (dimethylalkylammonium) 2 (phosphorylated betaine) were synthesized. The structure of compound 1 was confirmed by single crystal X-ray diffraction study. The antibacterial, antifungal, and ecotoxicological profiles of the synthesized compounds were evaluated against aquatic organisms and flowering plants. Both compounds demonstrated comparable toxicity toward Paramecium caudatum (Protista) and Ceriodaphnia affinis (Cladocera), with EC10 values of compound 1-0.62 g/L (P. caudatum), 0.13 g/L (C. affinis) and compound 2-0.90 g/L (P. caudatum), 0.08 g/L (C. affinis). These values indicate significantly lower toxicity compared to Benzalkonium chloride (BC) control (EC10 = 110 μg/L for P. caudatum, 30 μg/L for C. affinis). Neither compound exhibited toxicity toward the green alga Chlorella vulgaris, whereas BC inhibited growth by 93%. However, both compounds 1 and 2 inhibited Raphanus sativus seed germination at 10.0 g/L, whereas BC exhibited only marginal phytotoxicity even at this high concentration (10 g/L). According to the disk diffusion method, compound 1 exhibited superior activity against all tested isolates Bacillus subtilis (Gram-positive), Pseudomonas fluorescens (Gram-negative) and Fusarium sp. (micromycete). Compound 2 showed activity only against B. subtilis and Fusarium sp. at 10.0 g/L. Compound 1 inhibited microbial growth significantly more effectively than BC across all three microorganisms, while compound 2 performance did not differ substantially from the control. Thus, the synthesized compound 1-demonstrates antimicrobial efficacy comparable to reference compounds (Miramistin, Benzalkonium Chloride) while exhibiting substantially lower ecotoxicity. This enhanced safety profile suggests its production and application would pose reduced environmental risks.

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来源期刊
Current Microbiology
Current Microbiology 生物-微生物学
CiteScore
4.80
自引率
3.80%
发文量
380
审稿时长
2.5 months
期刊介绍: Current Microbiology is a well-established journal that publishes articles in all aspects of microbial cells and the interactions between the microorganisms, their hosts and the environment. Current Microbiology publishes original research articles, short communications, reviews and letters to the editor, spanning the following areas: physiology, biochemistry, genetics, genomics, biotechnology, ecology, evolution, morphology, taxonomy, diagnostic methods, medical and clinical microbiology and immunology as applied to microorganisms.
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