Milena Santos Aguiar, A. L. Carvalho, Elizama Aguiar Oliveira
{"title":"licuri [Syagrus coronata - (Martius) Beccari]残基培养放线菌产生的淀粉酶、脂肪酶和木聚糖酶的特性","authors":"Milena Santos Aguiar, A. L. Carvalho, Elizama Aguiar Oliveira","doi":"10.31668/rbc.v12i0.13183","DOIUrl":null,"url":null,"abstract":"In order to seach for different microbial sources of enzymes, Arthrobacter polychromogenes CDPI-30 and Streptomyces violaceoruber CDPA-32 were individually cultivated in licuri [Syagrus coronata - (Martius) Beccari] residues. It was possible to detect some enzymes but amylase, lipase and xylanase were selected for a basic characterization. The optimum conditions were observed at pH 6 and 7 and 40 – 70 °C for amylases, pH 4 – 6 and 50 – 90 °C for lipases and pH 8 and 10 and 20 – 50 °C for xylanases. The best stabilities, evaluated under different conditions were, in a way, a result from the optimal conditions. Additionally, substrate saturation was not observed for soluble starch and xylan until 15 mg/mL and p-nitrophenyl palmitate until 9.95 µmol/mL. These results indicate that both, actinobacteria and the agroindustrial residues, are good choices to produce basic industrial enzymes.","PeriodicalId":395269,"journal":{"name":"Revista de Biotecnologia & Ciência (ISSN 2238-6629)","volume":"86 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Characterization of amylase, lipase and xylanase produced by actinobacteria cultivated in licuri [Syagrus coronata - (Martius) Beccari] residues\",\"authors\":\"Milena Santos Aguiar, A. L. Carvalho, Elizama Aguiar Oliveira\",\"doi\":\"10.31668/rbc.v12i0.13183\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In order to seach for different microbial sources of enzymes, Arthrobacter polychromogenes CDPI-30 and Streptomyces violaceoruber CDPA-32 were individually cultivated in licuri [Syagrus coronata - (Martius) Beccari] residues. It was possible to detect some enzymes but amylase, lipase and xylanase were selected for a basic characterization. The optimum conditions were observed at pH 6 and 7 and 40 – 70 °C for amylases, pH 4 – 6 and 50 – 90 °C for lipases and pH 8 and 10 and 20 – 50 °C for xylanases. The best stabilities, evaluated under different conditions were, in a way, a result from the optimal conditions. Additionally, substrate saturation was not observed for soluble starch and xylan until 15 mg/mL and p-nitrophenyl palmitate until 9.95 µmol/mL. These results indicate that both, actinobacteria and the agroindustrial residues, are good choices to produce basic industrial enzymes.\",\"PeriodicalId\":395269,\"journal\":{\"name\":\"Revista de Biotecnologia & Ciência (ISSN 2238-6629)\",\"volume\":\"86 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revista de Biotecnologia & Ciência (ISSN 2238-6629)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31668/rbc.v12i0.13183\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista de Biotecnologia & Ciência (ISSN 2238-6629)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31668/rbc.v12i0.13183","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Characterization of amylase, lipase and xylanase produced by actinobacteria cultivated in licuri [Syagrus coronata - (Martius) Beccari] residues
In order to seach for different microbial sources of enzymes, Arthrobacter polychromogenes CDPI-30 and Streptomyces violaceoruber CDPA-32 were individually cultivated in licuri [Syagrus coronata - (Martius) Beccari] residues. It was possible to detect some enzymes but amylase, lipase and xylanase were selected for a basic characterization. The optimum conditions were observed at pH 6 and 7 and 40 – 70 °C for amylases, pH 4 – 6 and 50 – 90 °C for lipases and pH 8 and 10 and 20 – 50 °C for xylanases. The best stabilities, evaluated under different conditions were, in a way, a result from the optimal conditions. Additionally, substrate saturation was not observed for soluble starch and xylan until 15 mg/mL and p-nitrophenyl palmitate until 9.95 µmol/mL. These results indicate that both, actinobacteria and the agroindustrial residues, are good choices to produce basic industrial enzymes.