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1.
Chemosphere ; 296: 134076, 2022 Jun.
Article in English | MEDLINE | ID: mdl-35216985

ABSTRACT

The increase in human population determines a higher proteins request to sustain the feed demand for animals and aquaculture. Single Cell Proteins (SCPs) consist of mixed protein from pure and mixed culture of bacteria, fungi, algae, and yeast, which are grown and harvested to accomplish the food requirement of human and animals. This work investigated the production of Saccharomyces cerevisiae to be used as SCPs for animal feeding. The effluent of candies production process, rich in sugars, about 40 g/L, and agricultural digestate rich in nitrogen and other macro and micronutrients, were used for the yeast's growth. Preliminary batch tests demonstrated that aerobic conditions optimized the biomass growth. Then, continuous aerobic tests were conducted at different dilution rates. The dilution rate of 0.50 d-1, corresponding to a hydraulic retention time of 2 days, optimized both the biomass productivity of 0.25 g/L per day and the protein content of 28% w/w. The analysis of the aminoacidic profile demonstrated that obtained SCPs could be used as an integrator of feed for fish and monogastric animals. On the contrary, they were not suitable for pet feed as all the amino acids concentrations were lower than required standards. These results suggested that anaerobic digesters in the agricultural sector can be transformed into small biorefineries for microbial protein production.


Subject(s)
Dietary Proteins , Saccharomyces cerevisiae , Anaerobiosis , Animals , Biomass , Bioreactors , Food Handling
2.
Arch Microbiol ; 199(7): 991-1001, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28382474

ABSTRACT

Coal open pit mining in the South of Santa Catarina state (Brazil) was inappropriately developed, affecting approximately 6.700 ha. Re-vegetation is an alternative for the recovery of these areas. Furthermore, the use of herbaceous legumes inoculated with nitrogen fixing bacteria is motivated due to the difficulty implementing a vegetation cover in these areas, mainly due to low nutrient availability. Therefore, the aim of this work was to evaluate, among 16 autochthonous rhizobia isolated from the coal mining areas, those with the greatest potential to increase growth of the herbaceous legumes Vicia sativa and Calopogonium mucunoides. Tests were conducted in greenhouse containing 17 inoculation treatments (16 autochthonous rhizobia + Brazilian recommended strain for each plant species), plus two treatments without inoculation (with and without mineral nitrogen). After 60 days, nodulation, growth, N uptake, and symbiotic efficiency were evaluated. Isolates characterization was assessed by the production of indole acetic acid, ACC deaminase, siderophores, and inorganic phosphate solubilization. The classification of the isolates was performed by 16 S rDNA gene sequencing. Only isolates UFSC-M4 and UFSC-M8 were able to nodulate C. mucunoides. Among rhizobia capable of nodulating V. sativa, only UFSC-M8 was considered efficient. It was found the presence of more than one growth-promoting attributes in the same organism, and isolate UFSC-M8 presented all of them. Isolates were classified as belonging to Rhizobium, Burkholderia and Curtobacterium. The results suggest the inoculation of Vicia sativa with strain UFSC-M8, classified as Rhizobium sp., as a promising alternative for the revegetation of coal mining degraded areas.


Subject(s)
Actinobacteria/classification , Burkholderia/classification , Fabaceae/microbiology , Rhizobium/classification , Root Nodules, Plant/microbiology , Vicia sativa/microbiology , Actinobacteria/genetics , Actinobacteria/isolation & purification , Brazil , Burkholderia/genetics , Burkholderia/isolation & purification , Carbon-Carbon Lyases/metabolism , Coal , DNA, Ribosomal/genetics , Indoleacetic Acids/metabolism , Nitrogen Fixation , RNA, Ribosomal, 16S/genetics , Rhizobium/genetics , Rhizobium/isolation & purification , Symbiosis/genetics , Vicia sativa/growth & development
3.
Bioprocess Biosyst Eng ; 35(7): 1067-79, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22349925

ABSTRACT

Schizophyllum commune produces phytase through solid-state fermentation using different agroindustrial residues. After optimization of phytase production, a maximal level of phytase (113.7 Units/gram of dry substrate) was obtained in wheat bran based medium containing 5% sucrose, 50% humidity, 7.5% of biomass at 33 °C pH 7.0 during 72 h and a 285% improvement in enzyme titre was achieved. Analysis of fermentation parameters profile for phytase production showed the highest productivity (1.466 Units/gram of dry substrate/hour) in 66 h of fermentation. Phytase has an optimal pH of 5.0, an optimal temperature of 50 °C and K (m) and V (max) values of 0.16 mM and 1.85 µmol mL(-1) min(-1), respectively. Phytase activity was stimulated essentially in the presence of K(+), Ca(2+), Mg(2+), Mn(2+), Zn(2+), Cu(2+), Fe(2+), Fe(3+), Co(2+), Ni(2+), acetate and citrate at concentrations of 1 mM. Phytase had the best shelf life when stored at a cooling temperature, maintaining 38% of its initial activity after 112 days of storage, and still presenting enzymatic activity after 125 days of storage. Stability studies of phytase performed in aqueous enzyme extracts showed satisfactory results using polyethyleneglycol 3350, carboxymethylcellulose, methylparaben, mannitol and benzoic acid in concentrations of 0.25, 0.025, 0.025, 0.25, and 0.0025%, respectively. PEG 3350 was shown to be the best stabilizing agent, resulting in 109% of phytase activity from the initial crude extract remaining activity in after 90 days.


Subject(s)
6-Phytase/biosynthesis , Fermentation , Schizophyllum/enzymology , 6-Phytase/metabolism , Biomass , Enzyme Stability , Hot Temperature , Hydrogen-Ion Concentration , Substrate Specificity
4.
Braz. arch. biol. technol ; 54(6): 1069-1074, Nov.-Dec. 2011. ilus, tab
Article in English | LILACS | ID: lil-608427

ABSTRACT

A new formulated product containing high yield of phytase from Schizophyllum sp., an important mushroom used for medicinal studies, was developed for application in feed industries and for future use in food processing. The enzyme presented a high activity yield 55.5 U/mL and 6240 U/gds in liquid and solid formulated product, respectively. It showed a good shelf-life in concentrated product, retaining 67.8 percent of its activity after 60 days of storage at room temperature and 90 percent of the activity was maintained in the liquid formulation after the same period. Powder bioformulated product maintained 77 percent of its activity after two months of storage, without the addition of chemical additives, which was named as a new bioformulated product containing high quantities of phytase. After separation and concentration steps, enzyme stability was monitored in two forms: liquid and solid. The liquid product was stable with the presence of manitol and polyethylene glycol at 1 percent (w/v), while solid product was the most stable product without the presence of chemical additives.

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