海洋海绵相关菌抗白色念珠菌代谢产物的筛选

P. Kusumawati, Y. B. Murti, N. Wijayanti
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引用次数: 0

摘要

本研究从海洋海绵中分离的10种细菌中筛选出抗白色念珠菌活性较高的细菌。利用基础培养基培养细菌以产生提取物。用最小抑制浓度(MIC)微稀释肉汤作为抗ca测定,然后用薄层色谱-直接生物自显影法用喷雾试剂表征其活性成分。细菌鉴定采用重复元素序列pcr (rep-PCR)和16S rDNA部分基因序列扩增的分子方法,继续进行BLAST分析。在BYT5C4、BYT5C5、BYT1A和BYT7基础培养基上,对7.5×106 CFU/mL CA的MIC均为1 mg/mL,具有较高的抗CA活性。tlc -生物autography试验结果表明,各菌株的代谢产物均具有不同的Rf和代谢产物类型。Rep-PCR检测结果显示,4种细菌的相似指数较低,表明它们是不同的物种。分子鉴定结果表明,BYT5C4、BYT5C5、BYT1A、BYT7分离株分别与干酪短杆菌、深革Exiguobacterium exigundum、lylae微球菌、firmus芽孢杆菌有密切的亲缘关系。本研究中鉴定的活性代谢物可以分离确定活性分子及其对真菌生长的抑制途径。值得注意的是,可能需要进行进一步的研究,将每种抗真菌代谢物的活性与植物提取物中检测到的多种抗真菌代谢物的协同活性进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Screening of anti-Candida albicans metabolites produced by marine sponge-associated bacteria
This study selected bacteria with high anti-Candida albicans (CA) activity among ten bacteria isolated from marine sponges. Bacteria were cultivated using the basal medium to produce the extract. Minimum Inhibitory Concentration (MIC) microdilution broth was used as an anti-CA assay followed by TLC-direct bioautography to characterize their active compound with spray reagents. The bacteria determination was done by molecular approaches using Repetitive-Element Sequences-based-PCR (rep-PCR) and amplification of 16S rDNA partial gene sequences, continued with BLAST analysis. The four out of ten tested bacteria had high anti-CA compounds and were potentially to be produced on a larger scale using the basal medium, which was BYT5C4, BYT5C5, BYT1A, and BYT7, with MIC of 1 mg/mL against 7.5×106 CFU/mL CA. TLC-bioautography test results showed that all metabolites from each isolate had different Rf and types of metabolites. Rep-PCR test showed that four bacteria had a low similarity index, indicating that they were different species. Based on molecular identification results, the BYT5C4, BYT5C5, BYT1A, and BYT7 isolates are strictly related to Brevibacterium casei, Exiguobacterium profundum, Micrococcus lylae, and Bacillus firmus, respectively. The active metabolites identified in this study can be isolated to determine the active molecules and their inhibitory routes to fungal growth. It is worth noting that additional research might be conducted to compare the activity of each antifungal metabolite to the synergistic activity of numerous antifungal metabolites detected in plant extracts.
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