Yörük Emre, Danışman Zeynep, Pekmez Murat, Yli-Mattila Tapani
Department of Molecular Biology and Genetics, Faculty of Arts and Sciences, Istanbul Yeni Yuzyil University, Cevizlibag, Istanbul 34010, Turkey.
Programme of Molecular Biotechnology and Genetics, Institute of Graduate Studies in Sciences, Istanbul University, Suleymaniye, Istanbul 34116, Turkey.
Pathogens. 2024 May 8;13(5):395. doi: 10.3390/pathogens13050395.
In this study, the antifungal activity of cumin seed oil (CSO) was tested on . (i) Minimum inhibitory concentrations (MICs) and related concentrations (IC, IC, and IC) were detected; (ii) toxicity was evaluated by a water-soluble tetrazolium salt-1 (WST-1) assay; (iii) genomic/epigenomic alterations were evaluated by the coupled restriction enzyme digestion-random amplification (CRED-RA) method; (iv) oxidative stress was investigated by expression, catalase activity, and DCF-DA staining; (v) deoxynivalenol biosynthesis was evaluated by expression; (vi) and potential effects of CSO on wheat were tested by a water loss rate (WLR) assay. MIC, IC, IC and IC values were detected at 0.5, 0.375, 0.25, and 0.125 mg mL. In WST-1 assays, significant decreases ( < 0.001) were detected. Genomic template stability (GTS) related to methylation differences ranged from 94.60% to 96.30%. Percentage polymorphism for II/I values were as 9.1%/15.8%. (oxidative stress-related catalase) and (zinc finger motif transcription factor) gene expressions were recorded between 5.29 ± 0.74 and 0.46 ± 0.10 ( < 0.05). Increased catalase activity was detected ( < 0.05) by spectrophotometric assays. DCF-DA-stained (oxidative stressed) cells were increased in response to increased concentrations, and there were no significant changes in WLR values. It was concluded that CSO showed strong antifungal activity on via different physiological levels.
在本研究中,对孜然籽油(CSO)的抗真菌活性进行了如下测试:(i)检测最低抑菌浓度(MIC)及相关浓度(IC、IC和IC);(ii)通过水溶性四氮唑盐-1(WST-1)测定法评估毒性;(iii)通过限制性内切酶消化-随机扩增偶联(CRED-RA)方法评估基因组/表观基因组改变;(iv)通过表达、过氧化氢酶活性和DCF-DA染色研究氧化应激;(v)通过表达评估脱氧雪腐镰刀菌烯醇生物合成;(vi)通过失水率(WLR)测定法测试CSO对小麦的潜在影响。在0.5、0.375、0.25和0.125 mg/mL下检测到MIC、IC、IC和IC值。在WST-1测定中,检测到显著下降(<0.001)。与甲基化差异相关的基因组模板稳定性(GTS)范围为94.60%至96.30%。II/I值的多态性百分比分别为9.1%/15.8%。(氧化应激相关的过氧化氢酶)和(锌指基序转录因子)基因表达记录在5.29±0.74至0.46±0.10之间(<0.05)。通过分光光度法检测到过氧化氢酶活性增加(<0.05)。随着浓度增加,DCF-DA染色的(氧化应激)细胞增多,且WLR值无显著变化。得出的结论是,CSO通过不同生理水平对表现出强大的抗真菌活性。