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GSU1771调控硫还原地杆菌中的细胞外电子传递和电活性生物膜形成:遗传与电化学表征

GSU1771 regulates extracellular electron transfer and electroactive biofilm formation in Geobacter sulfurreducens: Genetic and electrochemical characterization.

作者信息

Hernández-Eligio Alberto, Huerta-Miranda Guillermo Antonio, Martínez-Bahena Sergio, Castrejón-López Dulce, Miranda-Hernández Margarita, Juárez Katy

机构信息

Departamento de Ingeniería Celular y Biocatálisis, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Av. Universidad 2001. Col. Chamilpa, 62210 Cuernavaca, Morelos, México; CONACyT, Ciudad de México, México.

Instituto de Energías Renovables, Universidad Nacional Autónoma de México, Priv. Xochicalco, 62580 Temixco, Morelos, México.

出版信息

Bioelectrochemistry. 2022 Jun;145:108101. doi: 10.1016/j.bioelechem.2022.108101. Epub 2022 Mar 21.

Abstract

Type IV pili and the >100c-type cytochromes in Geobacter sulfurreducens are essential for extracellular electron transfer (EET) towards metal oxides and electrodes. A previous report about a mutation in the gsu1771 gene indicated an enhanced reduction of insoluble Fe(III) oxides coupled with increased pilA expression. Herein, a marker-free gsu1771-deficient mutant was constructed and characterized to assess the role of this regulator in EET and the formation of electroactive biofilms. Deleting this gene delayed microbial growth in the acetate/fumarate media (electron donor and acceptor, respectively). However, this mutant reduced soluble and insoluble Fe(III) oxides more efficiently. Heme staining, western blot, and RT-qPCR analyses demonstrated that GSU1771 regulates the transcription of several genes (including pilA) and many c-type cytochromes involved in EET, suggesting the broad regulatory role of this protein. DNA-protein binding assays indicated that GSU1771 directly regulates the transcription of pilA, omcE, omcS, and omcZ. Additionally, gsu1771-deficient mutant biofilms are thicker than wild-type strains. Electrochemical studies revealed that the current produced by this biofilm was markedly higher than the wild-type strains (approximately 100-fold). Thus, demonstrating the role of GSU1771 in the EET pathway and establishing a methodology to develop highly electroactive G. sulfurreducens mutants.

摘要

嗜硫还原地杆菌中的IV型菌毛和100多种c型细胞色素对于向金属氧化物和电极的细胞外电子转移(EET)至关重要。先前一份关于gsu1771基因突变的报告表明,不溶性Fe(III)氧化物的还原增强,同时pilA表达增加。在此,构建并表征了一个无标记的gsu1771缺陷型突变体,以评估该调节因子在EET和电活性生物膜形成中的作用。删除该基因会延迟乙酸盐/富马酸盐培养基(分别为电子供体和受体)中的微生物生长。然而,该突变体更有效地还原了可溶性和不溶性Fe(III)氧化物。血红素染色、蛋白质印迹和RT-qPCR分析表明,GSU1771调节几个基因(包括pilA)以及许多参与EET的c型细胞色素的转录,表明该蛋白具有广泛的调节作用。DNA-蛋白质结合试验表明,GSU1771直接调节pilA、omcE、omcS和omcZ的转录。此外,gsu1771缺陷型突变体生物膜比野生型菌株更厚。电化学研究表明,该生物膜产生的电流明显高于野生型菌株(约100倍)。因此,证明了GSU1771在EET途径中的作用,并建立了一种开发高电活性嗜硫还原地杆菌突变体的方法。

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