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运动性影响大肠杆菌中的生物膜结构。

Motility influences biofilm architecture in Escherichia coli.

作者信息

Wood Thomas K, González Barrios Andrés F, Herzberg Moshe, Lee Jintae

机构信息

Department of Chemical Engineering, Texas A & M University, College Station, TX 77843-3122, USA.

出版信息

Appl Microbiol Biotechnol. 2006 Sep;72(2):361-7. doi: 10.1007/s00253-005-0263-8. Epub 2006 Jan 6.

Abstract

Eight Escherichia coli strains were studied in minimal medium with a continuous flow system using confocal microscopy. K12 wild-type strains ATCC 25404 and MG1655 formed the best biofilms ( approximately 43 microm thick, 21 to 34% surface coverage). JM109, DH5alpha, and MG1655 motA formed intermediate biofilms ( approximately 13 microm thick, 41 to 58% surface coverage). BW25113, MG1655 qseB, and MG1655 fliA had poor biofilms (surface coverage less than 5%). The best biofilm-formers, ATCC 25404 and MG1655, displayed the highest motility, whereas the worst biofilm former, BW25113, was motility-impaired. The differences in motility were due to differences in expression of the motility loci qseB, flhD, fliA, fliC, and motA (e.g., qseB expression in MG1655 was 139-fold higher than BW25113 and 209-fold higher than JM109). Motility affected the biofilm architecture as those strains which had poor motility (E. coli JM109, E. coli MG1655 motA, and DH5alpha) formed flatter microcolonies compared with MG1655 and ATCC 25404, which had more dramatic vertical structures as a result of their enhanced motility. The presence of flagella was also found to be important as qseB and fliA mutants (which lack flagella) had less biofilm than the isogenic paralyzed motA strain (threefold less thickness and 15-fold less surface coverage).

摘要

使用共聚焦显微镜在连续流动系统的基本培养基中对8株大肠杆菌菌株进行了研究。K12野生型菌株ATCC 25404和MG1655形成的生物膜最佳(约43微米厚,表面覆盖率21%至34%)。JM109、DH5α和MG1655 motA形成中等生物膜(约13微米厚,表面覆盖率41%至58%)。BW25113、MG1655 qseB和MG1655 fliA的生物膜较差(表面覆盖率小于5%)。最佳生物膜形成者ATCC 25404和MG1655具有最高的运动性,而最差的生物膜形成者BW25113运动性受损。运动性的差异是由于运动基因座qseB、flhD、fliA、fliC和motA表达的差异(例如,MG1655中qseB的表达比BW25113高139倍,比JM109高209倍)。运动性影响生物膜结构,与MG1655和ATCC 25404相比,运动性较差的菌株(大肠杆菌JM109、大肠杆菌MG1655 motA和DH5α)形成的微菌落更扁平,由于其运动性增强,MG1655和ATCC 25404具有更显著的垂直结构。还发现鞭毛的存在很重要,因为qseB和fliA突变体(缺乏鞭毛)的生物膜比同基因的运动性麻痹的motA菌株少(厚度少三倍,表面覆盖率少15倍)。

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