INTERACTIONS BETWEEN COLICINOGENIC FACTOR B AND F-TYPE FACTORS: ISOLATION OF A MUTANT F-lac FACTOR INSENSITIVE TO THE EFFECT OF COLICINOGENIC FACTOR B

Genetics ◽  
1972 ◽  
Vol 70 (2) ◽  
pp. 205-213
Author(s):  
T Negrotti ◽  
R Nagel de Zwaig
Keyword(s):  
Transfer Factor ◽  
Common Site ◽  
Factor B ◽  
E Coli ◽  
Resistance Transfer ◽  
By Products

ABSTRACT An extrachromosomal factor, colicinogenic factor B (colB) inhibits expression of fertility functions of various F-type factors in strains of E. coli K12. Mutant F-lac factors simultaneously became insensitive to all the effects of colB as well as to similar actions exerted by a resistance transfer factor, R fi+. This suggests that a common site or activity necessary for the expression of several F functions is affected by products of both colB and R fi+.

scholarly journals Intestinal Metabolites Influence Macrophage Phagocytosis and Clearance of Bacterial Infection

2021 ◽  
Vol 11 ◽  
Author(s):  
Amy A. O’Callaghan ◽  
Elaine Dempsey ◽  
Namrata Iyer ◽  
Sarah Stiegeler ◽  
Kevin Mercurio ◽  
...  
Keyword(s):  
Bacterial Infection ◽  
Metabolic Flux ◽  
Marker Gene ◽  
Intestinal Lumen ◽  
Microbial Fermentation ◽  
Macrophage Phenotype ◽  
E Coli ◽  
Macrophage Phagocytosis ◽  
Infection Treatment ◽  
By Products

The metabolite-rich environment that is the intestinal lumen contains metabolic by-products deriving from microbial fermentation and host cell metabolism, with resident macrophages being constantly exposed to this metabolic flux. Succinate, lactate and itaconate are three metabolites secreted by primed macrophages due to a fragmented tri-carboxylic acid (TCA) cycle. Additionally, succinate and lactate are known by-products of microbial fermentation. How these metabolites impact biological functioning of resident macrophages particularly in response to bacterial infection remains poorly understood. We have investigated the potential influence of these metabolites on macrophage phagocytosis and clearance of Escherichia coli (E. coli) infection. Treatment of murine bone-marrow-derived macrophages (BMDMs) with succinate reduced numbers of intracellular E. coli early during infection, while lactate-treated BMDMs displayed no difference throughout the course of infection. Treatment of BMDMs with itaconate lead to higher levels of intracellular E. coli early in the infection with bacterial burden subsequently reduced at later time-points compared to untreated macrophages, indicative of enhanced engulfment and killing capabilities of macrophages in response to itaconate. Expression of engulfment mediators MARCKS, RhoB, and CDC42 were reduced or unchanged following succinate or lactate treatment and increased in itaconate-treated macrophages following E. coli infection. Nitric oxide (NO) levels varied while pro- and anti-inflammatory cytokines differed in secretory levels in all metabolite-treated macrophages post-infection with E. coli or in response to lipopolysaccharide (LPS) stimulation. Finally, the basal phenotypic profile of metabolite-treated macrophages was altered according to marker gene expression, describing how fluid macrophage phenotype can be in response to the microenvironment. Collectively, our data suggests that microbe- and host-derived metabolites can drive distinct macrophage functional phenotypes in response to infection, whereby succinate and itaconate regulate phagocytosis and bactericidal mechanisms, limiting the intracellular bacterial niche and impeding the pathogenesis of infection.

scholarly journals Elucidation and Characterization of New Chlorinated By-Products after Electrochemical Degradation of Hydrochlorothiazide Using Graphite–Poly Vinyl Chloride Electrode

Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 540
Author(s):  
Zainab Mussa ◽  
Fouad Al-Qaim ◽  
Ali Yuzir ◽  
Hirofumi Hara ◽  
Shamila Azman ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Treatment Process ◽  
Oxidation Process ◽  
Electrochemical Treatment ◽  
Electrochemical Process ◽  
Experimental Conditions ◽  
E Coli ◽  
Flight Mass Spectrometry ◽  
Negative Ionization ◽  
By Products

This paper describes an electrochemical treatment process of hydrochlorothiazide (HDZ) under different conditions such as initial concentration, sodium chloride and applied voltage. In this present study, HDZ was treated by electrochemical oxidation process using graphite-PVC composite electrode as anode and Platinum (Pt) as cathode. All results were analyzed using liquid chromatography-time of flight/mass spectrometry (LC-TOF/MS). It was found that at high applied voltages, and high amounts of NaCl, the electrochemical treatment process was more efficient. The removal% of HDZ was 92% at 5 V after 60 min. From the obtained results, the electrochemical oxidation process of HDZ followed pseudo first order with rate constant values ranged between 0.0009 and 0.0502 min−1, depending on the experimental conditions. Energy consumption was also considered in this study, it was ranged between 0.9058 and 5.56 Wh/mg using 0.5, 0.3 and 0.1 g NaCl within interval times of (10, 20, 30, 40, 50, 60, 70, and 80 min). Five chlorinated and one non-chlorinated by-products were formed and analyzed in negative ionization (NI) mode during the electrochemical process. Due to the strong oxidizing potential of the chlorine (Cl2) and hypochlorite ion (ClO−), HDZ and its by-products were removed after 140 min. Furthermore, a novel synthesis of chlorothiaizde as one of the new by-products was reported in this present study. Toxicity was impacted by the formation of the by-products, especially at 20 min. The inhibition percentage (I%) of E. coli bacteria was decreased to be the lowest value after 140 min.

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