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Inhibition of Serratia marcescens Smj-11 Biofilm Formation by Alcaligenes faecalis STN17 Crude Extract

机译:抑制Serratia Marcescens SMJ-11 Biofilm Cheacation By Alcaligenes Faecalis STN17粗提物

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Serratia marcescens biofilms are formed when they are bound to surfaces in aqueous environments. S. marcescens utilizes N-acylhomoserine lactone (AHL) as its quorum sensing signal molecule. The accumulation of AHL indicates the bacteria to produce matrices to form biofilms. Prodigiosin (2-methyl-3-pentyl-6-methoxyprodigiosin), which causes red pigmentation in the colonies, are also produced when the AHL reaches a certain threshold. The Alcaligenes faecalis STN17 crude extract is believed to inhibit quorum sensing in the S. marcescens Smj-11 and, thus, impedes its biofilm formation ability. A. faecalis STN17 was grown in marine broth, and ethyl acetate extraction was carried out. The crude compound of A. faecalis STN17 was diluted at high concentration (0.2-6.4 mg/mL) and was taken to confirm anti-biofilm activity through the crystal violet method in 96-wells plate. Then, the crude extract underwent purification using simple solvents partitioning test to discern the respective compounds that had the anti-biofilm activity under the crystal violet method. The crystal violet test showed that the crude did have anti-biofilm activity on S. marcescens Smj-11, but did not kill the cells. This finding signifies that the suppression of biofilm formation in S. marcescens by A. faecalis STN17 has a strong correlation. The partitioning test showed that A. faecalis STN17 crude extract has several compounds and only the compound(s) in chloroform showed activities. In conclusion, the crude extract of A. faecalis STN17 has the ability to inhibit S. marcescens Smj-11 biofilm formation.
机译:当它们被结合到在水性环境中的表面上形成粘质沙雷氏菌的生物膜。粘质沙雷氏菌利用的N-酰基高丝氨酸内酯(AHL)作为它的群体感应信号分子。 AHL的积累表明细菌产生的矩阵以形成生物膜。灵菌红素(2-甲基-3-戊基-6- methoxyprodigiosin),这会导致红的色素沉着在菌落中,当AHL达到特定阈值也产生。的粪产碱杆菌STN17粗提取物被认为可抑制群体感应在粘质沙雷氏菌SMJ-11,因此,阻碍了它的生物膜形成的能力。粪STN17生长于海洋肉汤和乙酸乙酯进行萃取。粪STN17的粗化合物在高浓度下(0.2-6.4毫克/毫升)稀释,并通过在96孔板中的结晶紫方法采取确认抗生物膜活性。然后,使用简单的溶剂划分测试粗提取物纯化后行辨别该有结晶紫方法下的抗生物膜活性的相应的化合物。结晶紫试验表明,粗确实有抗生物活性上粘质沙雷氏菌SMJ-11,但没有杀死细胞。这一发现意味着在粘质沙雷氏菌的生物膜形成由粪STN17抑制具有很强的相关性。分隔试验表明,粪STN17粗提取物具有几种化合物,仅化合物(S)的氯仿显示活动。总之,粪STN17的粗提取物具有抑制粘质沙雷氏菌SMJ-11生物膜形成的能力。

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