scholarly journals Experimental Challenges for Reduced Genomes: The Cell Model Escherichia coli

2019 ◽  
Vol 8 (1) ◽  
pp. 3 ◽  
Author(s):  
Masaomi Kurokawa ◽  
Bei-Wen Ying

Genome reduction, as a top-down approach to obtain the minimal genetic information essential for a living organism, has been conducted with bacterial cells for decades. The most popular and well-studied cell models for genome reduction are Escherichia coli strains. As the previous literature intensively introduced the genetic construction and application of the genome-reduced Escherichia coli strains, the present review focuses the design principles and compares the reduced genome collections from the specific viewpoint of growth, which represents a fundamental property of living cells and is an important feature for their biotechnological application. For the extended simplification of the genomic sequences, the approach of experimental evolution and concern for medium optimization are newly proposed. The combination of the current techniques of genomic construction and the newly proposed methodologies could allow us to acquire growing Escherichia coli cells carrying the extensively reduced genome and to address the question of what the minimal genome essential for life is.

2011 ◽  
Vol 322 (1) ◽  
pp. 25-33 ◽  
Author(s):  
Yumi Iwadate ◽  
Hirofumi Honda ◽  
Haruhiko Sato ◽  
Masayuki Hashimoto ◽  
Jun-ichi Kato

2006 ◽  
Vol 188 (14) ◽  
pp. 5145-5152 ◽  
Author(s):  
Masaru Tamura ◽  
Kangseok Lee ◽  
Christine A. Miller ◽  
Christopher J. Moore ◽  
Yukio Shirako ◽  
...  

ABSTRACT Inactivation or deletion of the RNase E-encoding rne gene of Escherichia coli results in the growth of bacterial cells as filamentous chains in liquid culture (K. Goldblum and D. Apirion, J. Bacteriol. 146:128-132, 1981) and the loss of colony-forming ability (CFA) on solid media. RNase E dysfunction is also associated with abnormal processing of ftsQAZ transcripts (K. Cam, G. Rome, H. M. Krisch, and J.-P. Bouché, Nucleic Acids Res. 24:3065-3070, 1996), which encode proteins having a central role in septum formation during cell division. We show here that RNase E regulates the relative abundances of FtsZ and FtsA proteins and that RNase E depletion results in decreased FtsZ, increased FtsA, and consequently an altered FtsZ/FtsA ratio. However, while restoration of the level of FtsZ to normal in rne null mutant bacteria reverses the filamentation phenotype, it does not restore CFA. Conversely, overexpression of a related RNase, RNase G, in rne-deleted bacteria restores CFA, as previously reported, without affecting FtsZ abundance. Our results demonstrate that RNase E activity is required to maintain a proper cellular ratio of the FtsZ and FtsA proteins in E. coli but that FtsZ deficiency does not account for the nonviability of cells lacking RNase E.


2016 ◽  
Vol 11 (9) ◽  
pp. 1934578X1601100 ◽  
Author(s):  
Takahiro Kato ◽  
Jung-Bum Lee ◽  
Futoshi Taura ◽  
Fumiya Kurosaki

Two genes involved in δ-guaiene biosynthesis in Aquilaria microcarpa, δ-guaiene synthase (GS) and farnesyl diphosphate synthase (FPS), were overexpressed in Escherichia coli cells. Immunoblot analysis revealed that the concentration of GS-translated protein was rather low in the cells transformed by solely GS while appreciable accumulation of the recombinant protein was observed when GS was coexpressed with FPS GS-transformed cells liberated only a trace amount of δ-guaiene (0.004 μg/mL culture), however, the concentration of the compound elevated to 0.08 μg/mL culture in the cells transformed by GS plus FPS δ-Guaiene biosynthesis was markedly activated when E. coli cells coexpressing GS and FPS were incubated in enriched Terrific broth, and the content of the compound increased to approximately 0.6 μg/mL culture. These results suggest that coexpression of FPS and GS in E. coli is required for efficient 6-guaiene production in the bacterial cells, and the sesquiterpene-producing activity of the transformant is appreciably enhanced in the nutrients-enriched medium.


2013 ◽  
Vol 13 (4) ◽  
pp. 1056-1062 ◽  
Author(s):  
Saeid Rezaeinejad ◽  
Volodymyr Ivanov

The physiological differences of individual cells of bacterial population may imply the existence of cell subpopulations with different sensitivity to chlorine, which may affect the efficiency of drinking water disinfection. The susceptibility of individual bacterial cells to chlorine was examined using flow cytometry. The inactivation of Escherichia coli cells by chlorine in the populations with specific growth rates of 0.2 and 0.9 h−1 was assessed using various viability indicators. Viability of bacterial cells was evaluated using membrane integrity propidium iodide (PI) dye, respiratory activity indicator of 5-cyano-2,3-ditolyl tetrazolium chloride (CTC) and membrane potential probe of DiBAC4(3). It was found that there were cell subpopulations of E. coli with different levels of susceptibility to chlorine. E. coli cell population with higher specific growth rate was more susceptible to chlorine. The CT values for inactivation of 99% of cells (CT99) in populations of E. coli with specific growth rates of 0.9 and 0.2 h−1 were 0.06 and 0.09 mg min l−1, respectively. Flow cytometry could be used to study the sensitivity of bacterial cells to the chemical agents.


2021 ◽  
Vol 6 (1) ◽  
pp. 17-19
Author(s):  
Tahsin Tabassum ◽  
Tasmin Tabassum ◽  
Nafisa Tabassum ◽  
Syeda Muntaka Maniha ◽  
Rashed Noor

nsertion of plasmids into the bacterial cells is of great significance especially in course of the transfer of drug resistance, virulence and other traits. Retention of plasmids within the host bacteria is therefore an important factor for bacterial homeostasis. Current study inferred the pBR322 plasmid stability within the Escherichia coli competent cells. The calcium chloride heat shock method was used for the transformation purpose. The plasmid retention phenomenon was assessed through the replica plating. The results positively showed the plasmid retention within E. coli.


1991 ◽  
Vol 19 (1) ◽  
pp. 68-70
Author(s):  
Giorgio Brandi ◽  
Piero Sestili ◽  
Andrea Guidarelli ◽  
Giuditta Fiorella Schiavano ◽  
Amedeo Albano ◽  
...  

The killing of Escherichia coli cells by H2O2 is higher when exposure to the oxidant is performed in a complete culture medium, as compared to saline. Whereas MgSO4, CaCl2, thiamine or glucose, added separately or in combination with the saline, had no effect on the cytotoxic response to H2O2, the cytotoxicity appeared highly dependent upon the presence of the casamino acids in the incubation medium. One of these amino acids, histidine, was found to greatly augment the toxicity of H2O2 in E. coli. This effect of histidine was also observed in mammalian cells. In fact, both the cytoxicity and the DNA damage produced by H2O2 in Chinese hamster ovary (CHO) cells were significantly increased by this amino acid.


mBio ◽  
2017 ◽  
Vol 8 (4) ◽  
Author(s):  
Issei Nishimura ◽  
Masaomi Kurokawa ◽  
Liu Liu ◽  
Bei-Wen Ying

ABSTRACT Genome size is determined during evolution, but it can also be altered by genetic engineering in laboratories. The systematic characterization of reduced genomes provides valuable insights into the cellular properties that are quantitatively described by the global parameters related to the dynamics of growth and mutation. In the present study, we analyzed a small collection of W3110 Escherichia coli derivatives containing either the wild-type genome or reduced genomes of various lengths to examine whether the mutation rate, a global parameter representing genomic plasticity, was affected by genome reduction. We found that the mutation rates of these cells increased with genome reduction. The correlation between genome length and mutation rate, which has been reported for the evolution of bacteria, was also identified, intriguingly, for genome reduction. Gene function enrichment analysis indicated that the deletion of many of the genes encoding membrane and transport proteins play a role in the mutation rate changes mediated by genome reduction. Furthermore, the increase in the mutation rate with genome reduction was highly associated with a decrease in the growth rate in a nutrition-dependent manner; thus, poorer media showed a larger change that was of higher significance. This negative correlation was strongly supported by experimental evidence that the serial transfer of the reduced genome improved the growth rate and reduced the mutation rate to a large extent. Taken together, the global parameters corresponding to the genome, growth, and mutation showed a coordinated relationship, which might be an essential working principle for balancing the cellular dynamics appropriate to the environment. IMPORTANCE Genome reduction is a powerful approach for investigating the fundamental rules for living systems. Whether genetically disturbed genomes have any specific properties that are different from or similar to those of natively evolved genomes has been under investigation. In the present study, we found that Escherichia coli cells with reduced genomes showed accelerated nucleotide substitution errors (mutation rates), although these cells retained the normal DNA mismatch repair systems. Intriguingly, this finding of correlation between reduced genome size and a higher mutation rate was consistent with the reported evolution of mutation rates. Furthermore, the increased mutation rate was quantitatively associated with a decreased growth rate, indicating that the global parameters related to the genome, growth, and mutation, which represent the amount of genetic information, the efficiency of propagation, and the fidelity of replication, respectively, are dynamically coordinated. IMPORTANCE Genome reduction is a powerful approach for investigating the fundamental rules for living systems. Whether genetically disturbed genomes have any specific properties that are different from or similar to those of natively evolved genomes has been under investigation. In the present study, we found that Escherichia coli cells with reduced genomes showed accelerated nucleotide substitution errors (mutation rates), although these cells retained the normal DNA mismatch repair systems. Intriguingly, this finding of correlation between reduced genome size and a higher mutation rate was consistent with the reported evolution of mutation rates. Furthermore, the increased mutation rate was quantitatively associated with a decreased growth rate, indicating that the global parameters related to the genome, growth, and mutation, which represent the amount of genetic information, the efficiency of propagation, and the fidelity of replication, respectively, are dynamically coordinated.


2020 ◽  
Vol 96 (3) ◽  
Author(s):  
Xiao-jing Chen ◽  
Zheng Zhang ◽  
Ya-jie Li ◽  
Li Zhuo ◽  
Duo-hong Sheng ◽  
...  

ABSTRACT Many endogenous plasmids carry no noticeable benefits for their bacterial hosts, and the persistence of these ‘cryptic plasmids’ and their functional impacts are mostly unclear. In this study, we investigated these uncertainties using the social bacterium Myxococcus fulvus 124B02 and its endogenous plasmid pMF1. pMF1 possesses diverse genes that originated from myxobacteria, suggesting a longstanding co-existence of the plasmid with various myxobacterial species. The curing of pMF1 from 124B02 had almost no phenotypic effects on the host. Laboratory evolution experiments showed that the 124B02 strain retained pMF1 when subcultured on dead Escherichia coli cells but lost pMF1 when subcultured on living E. coli cells or on casitone medium; these results indicated that the persistence of pMF1 in 124B02 was environment-dependent. Curing pMF1 caused the mutant to lose the ability to predate and develop fruiting bodies more quickly than the pMF1-containing strain after they were subcultured on dead E. coli cells, which indicated that the presence of pMF1 in M. fulvus 124B02 has some long-term effects on its host. The results provide some new insights into the persistence and impacts of cryptic plasmids in their natural bacterial cells.


2004 ◽  
Vol 55 (1) ◽  
pp. 137-149 ◽  
Author(s):  
Masayuki Hashimoto ◽  
Toshiharu Ichimura ◽  
Hiroshi Mizoguchi ◽  
Kimie Tanaka ◽  
Kazuyuki Fujimitsu ◽  
...  

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