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1.
Braz. arch. biol. technol ; 63: e20190243, 2020. tab, graf
Article in English | LILACS | ID: biblio-1132163

ABSTRACT

Abstract This study evaluated the production of endoxylanases by Streptomyces malaysiensis AMT-3 in submerged fermentation using by-products of the food industry at 28ºC. In shake-flasks experiments, the highest endoxylanase activity of 45.8 U.mL-1 was observed within 6 days in a medium containing (w/v) 2.5% wheat bran and 1.2% corn steep liquor. The same culture conditions were used to evaluate the enzyme production in a 2 L stirred tank reactor under different agitation (300, 450 and 600 rev.min-1) and aeration (30 and 60 L.h-1) conditions. The use of 450 rev.min-1 coupled to an aeration of 90 L.h-1 resulted on 81.3 U.mL-1 endoxylanase activity within 5 days. The effect of temperature and pH on endoxylanase activity and stability showed the highest activity at 60 ºC and pH 6.0. Zymography showed the presence of three xylanolytic bands with molecular masses of 690, 180 and 142 kDa. The results showed that the thermotolerant actinobacterial endoxylanase can be produced in high titers using by-product of the food industry.


Subject(s)
Streptomyces/enzymology , Temperature , Food Industry , Endo-1,4-beta Xylanases/biosynthesis , Fermentation
2.
Braz. j. microbiol ; 47(3): 603-609, July-Sept. 2016. graf
Article in English | LILACS | ID: lil-788982

ABSTRACT

ABSTRACT Streptomyces lunalinharesii strain 235 produces an antimicrobial substance that is active against sulfate reducing bacteria, the major bacterial group responsible for biofilm formation and biocorrosion in petroleum reservoirs. The use of this antimicrobial substance for sulfate reducing bacteria control is therefore a promising alternative to chemical biocides. In this study the antimicrobial substance did not interfere with the biofilm stability, but the sulfate reducing bacteria biofilm formation was six-fold smaller in carbon steel coupons treated with the antimicrobial substance when compared to the untreated control. A reduction in the most probable number counts of planktonic cells of sulfate reducing bacteria was observed after treatments with the sub-minimal inhibitory concentration, minimal inhibitory concentration, and supra-minimal inhibitory concentration of the antimicrobial substance. Additionally, when the treated coupons were analyzed by scanning electron microscopy, the biofilm formation was found to be substantially reduced when the supra-minimal inhibitory concentration of the antimicrobial substance was used. The coupons used for the biofilm formation had a small weight loss after antimicrobial substance treatment, but corrosion damage was not observed by scanning electron microscopy. The absence of the dsrA gene fragment in the scraped cell suspension after treatment with the supra-minimal inhibitory concentration of the antimicrobial substance suggests that Desulfovibrio alaskensis was not able to adhere to the coupons. This is the first report on an antimicrobial substance produced by Streptomyces active against sulfate reducing bacteria biofilm formation. The application of antimicrobial substance as a potential biocide for sulfate reducing bacteria growth control could be of great interest to the petroleum industry.


Subject(s)
Oxidation-Reduction , Streptomyces/physiology , Sulfates/metabolism , Biofilms , Antibiosis , Streptomyces/drug effects , Streptomyces/ultrastructure , Microbial Sensitivity Tests , Biofilms/growth & development , Biofilms/drug effects , Anti-Bacterial Agents/pharmacology
3.
Braz. j. microbiol ; 42(4): 1384-1389, Oct.-Dec. 2011. ilus
Article in English | LILACS | ID: lil-614599

ABSTRACT

Brewer's spent grain and corn steep liquor or yeast extract were used as the sole organic forms for proteinase production by Streptomyces malaysiensis in submerged fermentation. The influence of the C and N concentrations, as well as the incubation periods, were assessed. Eight proteolytic bands were detected through gelatin-gel-electrophoresis in the various extracts obtained from the different media and after different incubation periods, with apparent molecular masses of 20, 35, 43, 50, 70, 100, 116 and 212 kDa. The results obtained suggest an opportunity for exploring this alternative strategy for proteinases production by actinomycetes, using BSG and CSL as economically feasible substrates.


Subject(s)
Actinobacteria/enzymology , Actinobacteria/isolation & purification , Fermentation , Peptide Hydrolases/analysis , Saccharomyces cerevisiae/enzymology , Streptomyces/enzymology , Streptomyces/isolation & purification , Beer , Electrophoresis, Starch Gel , Food Samples , Industrial Microbiology , Methods , Methods , Zea mays
4.
Braz. j. microbiol ; 42(1): 49-56, Jan.-Mar. 2011. tab
Article in English | LILACS | ID: lil-571374

ABSTRACT

Litopenaeus vannamei, which is the most common shrimp species cultivated in the northeast of Brazil, is very susceptible to microbial diseases, and this consequently affects productivity. There are reports of bacteria, viruses and protozoa in these shrimp, but not fungi. This study aims to isolate and identify fungi present in shrimp Litopenaeus vannamei, and in their nursery waters, at two breeding farms in Brazil. The pathogenic potential of the isolates was assessed through the qualitative detection of proteases and aflatoxin B production. The 146 isolated fungi comprised 46 species. Aspergillus, Penicillium and Furarium were the three most relevant genera and Aspergillus flavus was the predominant species with a total of 33 isolates. Most of the isolated species are known as potentially pathogenic to humans and other animals. Eighteen isolates of A. flavus and two of A. parasiticus were able to produce aflatoxin B and 33 out of the 46 species produced protease, indicating that these fungi may also become pathogenic to shrimp and their consumers.


Subject(s)
Aflatoxins/analysis , Aflatoxins/isolation & purification , Biodiversity , Mitosporic Fungi/enzymology , Mitosporic Fungi/isolation & purification , Penaeidae/enzymology , Penaeidae/pathogenicity , Peptide Hydrolases/analysis , Peptide Hydrolases/isolation & purification , Diagnosis , Food Samples , Methods , Methods , Virulence
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