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首页> 外文期刊>RSC Advances >Biofilm activity, ammonia removal and cell growth of the heterotrophic nitrifier, Acinetobacter sp., facilitated by exogenous N-acyl-homoserine lactones
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Biofilm activity, ammonia removal and cell growth of the heterotrophic nitrifier, Acinetobacter sp., facilitated by exogenous N-acyl-homoserine lactones

机译:外源性N-酰基-高丝氨酸内酯促进异养硝化器不动杆菌的生物膜活性,氨去除和细胞生长

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In the present study, the heterotrophic nitrification–aerobic denitrification strain, Acinetobacter sp. JQ1004, was treated with three typical N -acyl-homoserine lactone (AHL) molecules (C6-HSL, C8-HSL, and 3-oxo-C10-HSL) during the nitrogen removal process. The effects of AHLs on biofilm formation, flocculation, extracellular polymeric substance characteristics, and nitrogen removal were investigated. Findings revealed that low concentrations of these three AHLs could promote ammonia removal and cell growth as follows: C8-HSL > C6-HSL > 3-oxo-C10-HSL, whereas high concentrations suppressed nitrogen removal. Transcript levels of the amoA gene in the heterotrophic nitrification process were detected by real-time PCR, indicating that the addition of each AHL with 10 nmol L ~(?1) could stimulate expression of amoA . Notably, the addition of C6-HSL at relative lowly concentrations significantly accelerated biofilm formation and self-aggregation of strain JQ1004. Many microbial-flocs were observed between cells using scanning electron microscopy when strains were dosed with 10 nmol L ~(?1) C6-HSL. Excitation emission matrix spectra revealed that the addition of C6-HSL and C8-HSL at 10 nmol L ~(?1) did not change the components and structures of the extracellular polymeric substance (EPS), but the fluorescence intensity of various components increased substantially. However, the addition of 3-oxo-C10-HSL reduced the fluorescence strength of EPS, which had no remarkable effect on biofilm formation, self-aggregation, and nitrogen removal of the strain.
机译:在本研究中,异养硝化-好氧反硝化菌株不动杆菌属。在脱氮过程中,JQ1004用三种典型的N-酰基-高丝氨酸内酯(AHL)分子(C6-HSL,C8-HSL和3-oxo-C10-HSL)处理。研究了AHL对生物膜形成,絮凝,细胞外聚合物质特征和脱氮的影响。研究发现,低浓度的这三种AHL可以促进氨的去除和细胞生长,如下所示:C8-HSL> C6-HSL> 3-oxo-C10-HSL,而高浓度则抑制了氮的去除。通过实时荧光定量PCR检测异养硝化过程中amoA基因的转录水平,这表明在每个AHL中加入10 nmol L〜(?1)可以刺激amoA的表达。值得注意的是,以相对较低的浓度添加C6-HSL可以显着加速菌株JQ1004的生物膜形成和自聚集。当使用10 nmol L〜(?1)C6-HSL进行菌株接种时,使用扫描电子显微镜在细胞之间观察到许多微生物絮凝物。激发发射矩阵光谱表明,在10 nmol L〜(?1)处添加C6-HSL和C8-HSL不会改变细胞外聚合物(EPS)的成分和结构,但各种成分的荧光强度显着增加。但是,添加3-oxo-C10-HSL降低了EPS的荧光强度,这对菌株的生物膜形成,自聚集和脱氮没有显着影响。

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