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      Proteomic profiles comparison of three isolated bacteria strains from a copper processing area

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      1 , , 1 , 1 , 1 , 1 , 1 , 1
      BMC Proceedings
      BioMed Central
      5th Congress of the Brazilian Biotechnology Society (SBBIOTEC)
      10-14 November 2013

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          Abstract

          Background Release of toxic metals is one of most significant environmental problems since industrial revolution, mainly because heavy metals are not degraded and, therefore, remain in the environment. Some natural ecosystems may contain high heavy metals concentrations and, thus, it is not surprising that genes resistance to heavy metals are easily found in bacteria living in these environmental samples [1]. Soils, sediments and waters contaminated with xenobiotics compounds are suitable substrates for isolation of these adapted microorganisms [2]. Thereby, proteome analysis has become a powerful tool for investigating global changes in prokaryotic gene expression. Once the two-dimensional electrophoresis (2-DE) displays all bacterial soluble proteins expressed at specific culture conditions on gel, high throughput screening of these induced proteins is possible. This study has a purpose to isolated bacteria that tolerate high concentrations of copper and compared their proteomic profiles. The understanding about the copper metabolic role of these microorganisms it will be helpful to improve bioprocesses of decontamination. Methods Microorganisms were isolated from mining wastes (samples of water and sediments) by culture enrichment technique; this procedure was repeated four times. Isolates were inoculated into MJS medium containing different concentrations of chloride copper (1mM, 2.5mM and 5mM) and incubated in plates for 72 h at 28°C. Strains have been identified by mass spectrometry equipment (MALDI-TOF) that produces a protein spectrum of each sample and then compares the obtained profile with a Biotyper data base. Cells were grown on MJS with and without copper (2.5 and 5 mM) incubated on an orbital shaker (150 rpm) at 28°C. The cells were collected in the exponential growth phase for extraction proteins procedure. Then, these citosolic proteins were analyzed using 2-DE technique, as described previously [3]. Results and conclusions Two bacteria strains were isolated from samples of sediment and one from water sample. Identification of strains isolated from sediment samples resulted in Pseudomonas aeruginosa and Acinetobacter pitii and from water sample also identified as Pseudomonas aeruginosa. Acinetobacter pitii and Pseudomonas aeruginosa (water sample) tolerated until 2.5 mM of copper and Pseudomonas aeruginosa from sediment sample tolerated 5 mM of copper. One study with Pseudomonas aeruginosa strain revealed this bacterium was able to tolerate only 0.77 mM of copper [4] and Andreazza et al., reported Acinetobacter sp. strain tolerated until 8 mM of copper. Pseudomonas aeruginosa and Acinetobacter pitii (from sediment samples) when grown up only in the MJS medium (without copper) expressed 206 and 247 proteins, respectively. Pseudomonas expressed 132 proteins when grown up in MJS with copper, where 38 were differentially expressed after copper exposure. Of the 188 proteins expressed by Acinetobacter (MJS with copper) 57 were expressed differentially. Pseudomonas aeruginosa (isolated from the water sample) reached the expression of 240 proteins (only in MJS medium). When grown up in MJS with copper, 80 proteins were expressed, where 65 proteins presented different expression after copper exposure. All these proteins may be involved in the resistance copper mechanism and the understanding of their metabolic role can be helpful for improve the bioremediation process.

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          Environmental selection of antibiotic resistance genes.

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            Profiling the proteome complement of the secretion from hypopharyngeal gland of Africanized nurse-honeybees (Apis mellifera L.).

            The protein complement of the secretion from hypopharyngeal gland of nurse-bees (Apis mellifera L.) was partially identified by using a combination of 2D-PAGE, peptide sequencing by MALDI-PSD/MS and a protein engine identification tool applied to the honeybee genome. The proteins identified were compared to those proteins already identified in the proteome complement of the royal jelly of the honey bees. The 2-D gel electrophoresis demonstrated this protein complement is constituted of 61 different polypepides, from which 34 were identified as follows: 27 proteins belonged to MRJPs family, 5 proteins were related to the metabolism of carbohydrates and to the oxido-reduction metabolism of energetic substrates, 1 protein was related to the accumulation of iron in honeybee bodies and 1 protein may be a regulator of MRJP-1 oligomerization. The proteins directly involved with the carbohydrates and energetic metabolisms were: alpha glucosidase, glucose oxidase and alpha amylase, whose are members of the same family of enzymes, catalyzing the hydrolysis of the glucosidic linkages of starch; alcohol dehydrogenase and aldehyde dehydrogenase, whose are constituents of the energetic metabolism. The results of the present manuscript support the hypothesis that the most of these proteins are produced in the hypoharyngeal gland of nurse-bees and secreted into the RJ.
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              Biosorption of chromium, copper, manganese and zinc by Pseudomonas aeruginosa AT18 isolated from a site contaminated with petroleum.

              The study describes the sorption of Cr, Cu, Mn and Zn by Pseudomonas aeruginosa AT18 isolated from a site contaminated with petroleum and heavy metals. The concentrations studied were 50, 49, 60 and 70 (mg L(-1)) for Cr, Cu, Mn and Zn, respectively. The solution pH and ionic strength were very important factors in the metal biosorption performance and the biosorption capacity of P. aeruginosa AT18 for Cr3+,Cu2+, Mn2+ and Zn2+. In aqueous solution, the biosorption increased with increasing pH in the range 5.46-7.72. The results obtained in the experimental assays show that P. aeruginosa AT18 has the capacity for biosorption of the metallic ions Cr3+, Cu2+ and Zn2+ in solutions, although its capacity for the sorption of manganese is low (22.39 mg Mn2+/g of biomass) in comparison to the Cr3+, Cu2+ and Zn2+ ions, as shown by the individual analyses. However, 20% of the manganese was removed from an initial concentration of 49.0 mg L(-1), with a Qm value similar to that obtained in solutions containing mixtures of Cr3+, Cu2+, Mn2+and Zn2+. The chromium level sorbed by P. aeruginosa AT18 biomass was higher than that for Cu, Mn and Zn, with 100% removal in the pH range 7.00-7.72 and a Qm of 121.90-200.00 mg of Cr3+/g of biomass. The removal of Cr, Cu and Zn is also a result of precipitation processes.
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                Author and article information

                Conference
                BMC Proc
                BMC Proc
                BMC Proceedings
                BioMed Central
                1753-6561
                2014
                1 October 2014
                : 8
                : Suppl 4
                : P197
                Affiliations
                [1 ]Center for Environmental Research and Training, CEPEMA-POLI-USP; University of São Paulo, Biomedical Sciences Institute, ICB-USP, SP, Brazil
                Article
                1753-6561-8-S4-P197
                10.1186/1753-6561-8-S4-P197
                4210680
                d8cf8005-5344-46be-acf9-8e04cd82664c
                Copyright © 2014 Gracioso et al.; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                5th Congress of the Brazilian Biotechnology Society (SBBIOTEC)
                Florianópolis, Brazil
                10-14 November 2013
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                Medicine
                Medicine

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