scholarly journals Improved ethanol productivity from lignocellulosic hydrolysates by Escherichia coli with regulated glucose utilization

2018 ◽  
Vol 17 (1) ◽  
Author(s):  
Jinfeng Sun ◽  
Kangming Tian ◽  
Jie Wang ◽  
Zixing Dong ◽  
Xiaoguang Liu ◽  
...  
Microbiology ◽  
2010 ◽  
Vol 156 (5) ◽  
pp. 1527-1537 ◽  
Author(s):  
Rosario Pérez-Redondo ◽  
Irene Santamarta ◽  
Roel Bovenberg ◽  
Juan F. Martín ◽  
Paloma Liras

Streptomyces clavuligerus ATCC 27064 is unable to use glucose but has genes for a glucose permease (glcP) and a glucose kinase (glkA). Transformation of S. clavuligerus 27064 with the Streptomyces coelicolor glcP1 gene with its own promoter results in a strain able to grow on glucose. The glcP gene of S. clavuligerus encodes a 475 amino acid glucose permease with 12 transmembrane segments. GlcP is a functional protein when expressed from the S. coelicolor glcP1 promoter and complements two different glucose transport-negative Escherichia coli mutants. Transcription studies indicate that the glcP promoter is very weak and does not allow growth on glucose. These results suggest that S. clavuligerus initially contained a functional glucose permease gene, like most other Streptomyces species, and lost the expression of this gene by adaptation to glucose-poor habitats.


2012 ◽  
Vol 51 (No. 3) ◽  
pp. 81-88 ◽  
Author(s):  
E. Skrivanova ◽  
M. Marounek ◽  
V. Benda ◽  
P. Brezina

The antimicrobial activity of fatty acids, monolaurin, citric, succinic, fumaric, malic and lactic acid was determined in cultures of two strains of Escherichia coli, three strains of Salmonella sp. and two strains of Clostridium perfringens. Antimicrobial activity was expressed as minimum inhibitory concentration (MIC) that prevented growth and glucose utilization in treated cultures. Caprylic acid was the only acid inhibiting glucose utilization in all cultures. Its MIC varied from 1 to 3 mg/ml. Strains CCM 3954 and CCM 4225 of E. coli were inhibited also by capric acid at 5 mg/ml. Strains CCM 4435<sup>T </sup>and CNCTC 5459 of Cl. perfringens were inhibited by medium-chain fatty acids (C<sub>8</sub> to C<sub>14</sub>), oleic acid and one strain also by linoleic acid. The minimum MICs were those of lauric and myristic acid (between 0.1 and 0.2 mg/ml). Growth of Cl. perfringens, but not other bacteria, was inhibited also by monoglyceride of lauric acid (MIC = 3 mg/ml), and by citric acid (MIC = 4 mg/ml). Inhibitory effects of other acids were not observed at 5 mg/ml. Caprylic and lauric acid did not influence the K<sup>+ </sup>permeability of the cytoplasmic membrane in cells of E. coli CCM 4225 and Cl. perfringens CCM 4435<sup>T</sup>, respectively. In cultures of both strains of E. coli treated with caprylic acid at 5 mg/ml, and in those of Cl. perfringens CCM 4435<sup>T </sup>treated with lauric acid at 1 mg/ml, or with its monoglyceride at 5 mg/ml, the transmission electron microscopy revealed damage of cytoplasmatic structures. In cells of Cl. perfringens the separation of inner and outer membranes was apparent, the integrity of the outer membrane, however, was maintained. It can be concluded that medium-chain fatty acids are more efficient antimicrobials than other, more polar organic acids tested.


2020 ◽  
Vol 36 (3) ◽  
pp. 25-33
Author(s):  
A.Yu. Gulevich ◽  
V.G. Debabov

The characteristics of anaerobic glucose utilization and metabolite production by recombinant Escherichia coli strains with impaired fermentation ability upon respiration with pyruvate as an internal and nitrate as an external electron acceptor have been studied. It was found that respiration processes utilizing pyruvic acid as an endogenous electron acceptor and leading to the lactate and alanine formation were capable of mutual interference. After elimination of ammonium ions from the medium, the native activity levels of respiratory lactate dehydrogenases Did and LldD in E. coli strains deficient in the mixed acid fermentation pathways can almost completely compensate for the loss of activity of respiratory alanine dehydrogenase DadA, but are insufficient to maintain the entire intracellular redox balance. The addition of nitrate ions in the medium abolished alanine production by the strains despite the availability of ammonium ions, while the functionality of respiratory reduction of endogenous pyruvate to lactate retained in the studied strains even in the presence of a strong exogenous oxidant. Respiration with external electron acceptor provoked the activation of the oxidative tricarboxylic acid cycle in the strains. Anaerobic glucose utilization by the strain with interrupted tricarboxylic acid cycle increased during nitrate respiration, but remained restricted by the excessive generation of reducing equivalents in the residual reactions of the cycle. Escherichia coli, glucose, fermentation, respiration, pyruvate, lactate, alanine, nitrate, ammonium. The work was supported by a grant from the Russian Foundation for Basic Research (project #18-04-01222).


1987 ◽  
Vol 33 (1) ◽  
pp. 57-62 ◽  
Author(s):  
Matthew J. Domek ◽  
John E. Robbins ◽  
Mark E. Anderson ◽  
Gordon A. McFeters

Escherichia coli injured by copper in carbonate buffer simulating the drinking water environment showed decreased oxygen utilization. Oxygraph measurements revealed that copper-injured bacteria had a rate of oxygen utilization that was less than 25% of that of control cells. Respirometry experiments measured rates over a longer period of time and showed similar trends. Nuclear magnetic resonanance spectroscopy (13C nmr) and gas chromatography were used to identify differences in metabolism between healthy and injured populations of E. coli. The rate of glucose utilization by injured cells under anaerobic conditions was 64% of that of healthy cells. The rates of lactate and ethanol accumulation were 88 and 50% of the control, respectively. The 13C nmr studies of oxygenated cultures revealed differences in the accumulation of acetate and glutamine. Aerobic utilization of glucose and succinate by injured cells were 87 and 21% of the rate of the controls, respectively. Additional studies revealed injured cells had a decreased ability to reduce 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyltetrazolium chloride (INT) with a variety of carbohydrate substrates. Injured cells reduced greater quantities of INT than healthy cells when NADH was used as a substrate. A comparison of metabolic end products suggested that injured cells also had considerable differences in carbon flow compared with healthy cells.


2013 ◽  
Vol 690-693 ◽  
pp. 1370-1373
Author(s):  
Qing Hua Zhou ◽  
Juan Xie ◽  
Jing Cui ◽  
Yan Li

Simulating dynamic behaviors of metabolic networks of a living cell plays an important role in system biology. As a part of dynamic model, the choice of objective function has a large influence on simulation accuracy for these behaviors. In this work, in order to precisely describe the biomass yield and substrate utilization in glycolytic metabolism of Escherichia coli, we try to modify the objective function of the existing dynamic model by using maximization of glucose utilization to replace the traditional objective one. After that, the dynamic model with the new objective is converted to a standard optimal control problem. And then we compute such model through the use of the penalty function methods. The results illustrate that the simulation curves perfectly agree with experiment data, especially with biomass concentration. Thereby, we conclude that completely utilizing substrate glucose is feasible to describe and improve the simulation accuracy on concentrations of some important metabolites in Escherichia coli. The completeness of investigating such models will be helpful and instructive for the application of bioengineering.


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