Evidence of weak interaction between ferric iron and extracellular polymeric substances of Acidithiobacillus ferrooxidans

2022 ◽  
pp. 105817
Author(s):  
Bingxu Dong ◽  
Yan Jia ◽  
Haiping Zhao ◽  
Qiaoyi Tan ◽  
Heyun Sun ◽  
...  
2013 ◽  
Vol 825 ◽  
pp. 120-124 ◽  
Author(s):  
Albert Saavedra ◽  
Beatriz Pavez ◽  
Mauricio Diaz ◽  
Juan Carlos Gentina

The presence of extracellular polymeric substances (EPS) is important in the building of biofilms on mineral surfaces, increasing the bioleaching activity, as well as protecting the cells from adverse environmental conditions. The objective of this work was to study the effect of galactose in EPS production by Acidithiobacillus ferrooxidans. The experiences were performed in shake flask of 250 mL at 30 °C, 200 rpm and at an initial pH of 1.8. In order to establish the natural tolerance of the strain, its growth behaviour was evaluated at high ferric iron concentrations by adding consecutively the equivalent of 9 g/L of ferrous iron each time it was depleted in the broth. Cell growth stopped once ferric iron concentration increased up to 38 g/L. In order to determine the optimal conditions for EPS production, experiments were run in a chemostat of 0.5 L, operated at a constant dilution rate of 0.03 h-1. Different steady states were obtained varying feeding concentrations of galactose (0.15%; 0.25% and 0.35%) and carbon dioxide (180 ppm and 360 ppm). , Cells grown in the chemostat at optimum operation conditions were used as inoculum to determine oxidative capacity of the microorganisms overproducing EPS. The EPS was quantified using confocal laser scanning microscopy (CLSM), labelling the cells with propidium iodide and EPS carbohydrates with wheat germ agglutinin (WGA). The higher volume production of EPS was observed in cells grown using 360 ppm of CO2 and 0.35% of galactose. Also it was observed a size increment of cells, compared to cells grown in culture medium having 9 g/L of ferrous iron where presence of EPS was no detected. The results revealed that EPS overproducing A. ferrooxidans showed a tolerance to ferric iron concentration almost 9.5 g/L higher than the natural tolerance of cells grown in absence of galactose. Presence of galactose in culture medium stimulated the EPS production.


2011 ◽  
Vol 343-344 ◽  
pp. 920-925
Author(s):  
Jiang Lei

This paper deals with the surface characteristic of pyrrhotite bio-oxidized byAcidithiobacillus ferrooxidans. Large amounts of jarosite and element sulfur were determined in the bio-oxidation processe of pyrrhotite. More complicatedly, biofilm exists on the surface of pyrrhotite. This type of structured community ofA. ferrooxidanswas enclosed in the extracellular polymeric substances (EPS), and covered with the deposition generated in the bio-oxidation processe of pyrrhotite.


2016 ◽  
Vol 167 (5) ◽  
pp. 357-366 ◽  
Author(s):  
Jiri Kucera ◽  
Eva Pakostova ◽  
Jan Lochman ◽  
Oldrich Janiczek ◽  
Martin Mandl

2013 ◽  
Vol 825 ◽  
pp. 115-119 ◽  
Author(s):  
Albert Saavedra ◽  
Beatriz Pavez ◽  
Mauricio Diaz ◽  
Juan Carlos Gentina

The ability ofAcidithiobacillus ferrooxidansto get its energy from the oxidation of ferrous iron and the inhibitory effect of high ferric iron concentrations on its growth behaviour has been extensively studied. Furthermore it is known thatA. ferrooxidansexudes organic substances called extracellular polymeric substances (EPS), which could play a role in its protection against adverse environmental conditions. In this context, the aim of this work was to study the production of EPS during adaptation ofA. ferrooxidansto high ferric ion concentrations. The experiments were performed in shake flasks of 250 mL at 30 °C, 200 rpm and at an initial pH of 1.8. In order to establish the natural tolerance of the strain, its growth behaviour was evaluated at high ferric iron concentrations by adding consecutively the equivalent of 9 g/L of ferrous iron each time it was depleted in the broth. Cell growth stopped once ferric iron concentration increased up to 38 g/L. The adaptation consisted in eight sub-cultures run in parallel at initial concentrations of ferrous iron of 18, 27 and 36 g/L. The EPS was quantified as micro volumes using confocal laser scanning microscopy (CLSM), labelling the cells with propidium iodide and EPS carbohydrates with wheat germ agglutinin (WGA). During the adaptation procedure it was observed an increase in the ferric ion volumetric productivity of subcultures run with 27 and 36 g/L, as a result of cell adaptation. The amount of EPS exuded by cells was higher along with those experimental conditions having higher ferric iron concentrations. It was not detected EPS on cells grown on 9 g/L of ferrous iron. This study found that the adapted strain showed higher production of EPS at high ferric ion concentrations and higher ferric ion tolerance than non-adapted ones.


Microbiology ◽  
2005 ◽  
Vol 151 (6) ◽  
pp. 2005-2015 ◽  
Author(s):  
R. Quatrini ◽  
C. Lefimil ◽  
D. S. Holmes ◽  
E. Jedlicki

Acidithiobacillus ferrooxidans is a Gram-negative bacterium that lives at pH 2 in high concentrations of soluble ferrous and ferric iron, making it an interesting model for understanding the biological mechanisms of bacterial iron uptake and homeostasis in extremely acid conditions. A candidate fur AF (Ferric Uptake Regulator) gene was identified in the A. ferrooxidans ATCC 23270 genome. FurAF has significant sequence similarity, including conservation of functional motifs, to known Fur orthologues and exhibits cross-reactivity to Escherichia coli Fur antiserum. The fur AF gene is able to complement fur deficiency in E. coli in an iron-responsive manner. FurAF is also able to bind specifically to E. coli Fur regulatory regions (Fur boxes) and to a candidate Fur box from A. ferrooxidans, as judged by electrophoretic mobility shift assays. FurAF represses gene expression from E. coli Fur-responsive promoters fiu and fhuF when expressed at high protein levels. However, it increases gene expression from these promoters at low concentrations and possibly from other Fur-regulated promoters involved in iron-responsive oxidative stress responses.


2010 ◽  
Vol 99 (3) ◽  
pp. 609-617 ◽  
Author(s):  
Lúcio F. C. Ferraz ◽  
Leandro C. L. Verde ◽  
Renato Vicentini ◽  
Ana P. Felício ◽  
Marcelo L. Ribeiro ◽  
...  

Materials ◽  
2018 ◽  
Vol 11 (9) ◽  
pp. 1739 ◽  
Author(s):  
Yongwei Song ◽  
Yelin Liu ◽  
Heru Wang

Schwertmannite is an environmental mineral material that can promote the natural passivation of heavy metal elements, thereby reducing environmental pollution from toxic elements. However, the fundamental reason for the difference between the chemically (H2O2-FeSO4) and biologically (Acidithiobacillus ferrooxidans-FeSO4) synthesized schwertmannite is still unclear. In this study, X-ray diffraction, scanning electron microscopy, the Brunauer–Emmett–Teller method, and X-ray fluorescence spectrometry were used to compare the structure, specific surface area, and elemental composition of schwertmannite synthesized by biological and chemical methods. The removal capacity of As(III) by the two kinds of schwertmannite and the effects of extracellular polymeric substances (EPS) on biogenetic schwertmannite were also investigated. At a consistent Fe2+ oxidation efficiency, the chemical method synthesized more schwertmannite than the biological method over a 60-h period. The biosynthesized schwertmannite had a “chestnut shell” shape, with a larger particle size and specific surface than the chemically synthesized schwertmannite, which was relatively smooth. The saturated adsorption capacities of the biologically and chemically synthesized schwertmannite were 117.0 and 87.0 mg·g−1, respectively. After exfoliation of the EPS from A. ferrooxidans, the biosynthesized schwertmannite displayed a “wool ball” shape, with rough particle surfaces, many microporous structures, and a larger specific surface area. The schwertmannite yield also increased by about 45% compared with that before exfoliation, suggesting that the secretion of EPS by A. ferrooxidans can inhibit the formation of schwertmannite.


2006 ◽  
Vol 16 (4) ◽  
pp. 931-936 ◽  
Author(s):  
Hong-bo ZHOU ◽  
Xi LIU ◽  
Guan-zhou QIU ◽  
Jian-she LIU ◽  
Xin-hua CHEN

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