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1.
PLoS One ; 13(7): e0200660, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30016375

RESUMO

Hydrostatic pressure is an important physical stimulus which can cause various responses in bacterial cells. The survival and cellular processes of Escherichia coli under hydrostatic pressures between 10 MPa and 110 MPa have been studied. However, understanding bacterial responses to moderately elevated pressure of up to 10 MPa is useful for a range of different applications including for example in smart and responsive materials. In this study, the genetic responses of E. coli K-12 MG1655 to 1 MPa pressure was examined using transcriptomic analysis by RNA-Seq. The results show that 101 genes were differentially expressed under 1 MPa pressure in E. coli cells, with 85 of them up-regulated. The analysis suggested that some genes were over expressed to adapt the increase of oxygen levels in our system, and several functional categories are involved including oxidative stress responses, Fe-S cluster assembly and iron acquisition. Two differentially expressed genes azuC and entC were further investigated using RT-qPCR, and GFP reported strains of those two genes were created, AG1319 (PazuC azuC-msfgfp) and AG1321 (PentC entC-msfgfp). A linear response of azuC expression was observed between 0 MPa to 1 MPa by monitoring the fluorescence signal of strain AG1319 (PazuC azuC-msfgfp). This study is the first report to demonstrate the genetic response of bacterial cells under 1 MPa hydrostatic pressure, and provides preliminary data for creating pressure sensing bacterial strains for a wide range of applications.


Assuntos
Escherichia coli K12/metabolismo , Proteínas de Escherichia coli/biossíntese , Regulação Bacteriana da Expressão Gênica , Estresse Oxidativo , Escherichia coli K12/genética , Proteínas de Escherichia coli/genética , Pressão Hidrostática
2.
Bioinspir Biomim ; 13(4): 046004, 2018 05 25.
Artigo em Inglês | MEDLINE | ID: mdl-29652250

RESUMO

In this paper, we describe the first steps in the design of a synthetic biological system based on the use of genetically modified bacteria to detect elevated pressures in soils and respond by cementing soil particles. Such a system might, for example, enable a self- constructed foundation to form in response to load using engineered bacteria which could be seeded and grown in the soils. This process would reduce the need for large-scale excavations and may be the basis for a new generation of self-assembling and responsive bio-based materials. A prototype computational model is presented which integrates experimental data from a pressure sensitive gene within Escherichia coli bacteria with geotechnical models of soil loading and pore water pressure. The results from the integrated model are visualised by mapping expected gene expression values onto the soil volume. We also use our experimental data to design a two component system where one type of bacteria acts as a sensor and signals to another material synthesis bacteria. The simulation demonstrates the potential of computational models which integrate multiple scales from macro stresses in soils to the expression of individual genes to inform new types of design process. The work also illustrates the combination of in silico (silicon based computing) computation with in vivo (in the living) computation.


Assuntos
Microbiologia do Solo , Solo/química , Biologia Sintética , Adesividade , Bioengenharia , Materiais Biomiméticos , Biomimética , Simulação por Computador , Escherichia coli/genética , Escherichia coli/fisiologia , Genes Bacterianos , Genes Reporter , Proteínas de Fluorescência Verde/genética , Fenômenos Mecânicos , Pressão , Regulação para Cima
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