{"title":"紫色链霉菌BF 3.10甘露聚糖酶水解Porang生产甘露寡糖","authors":"A. Safitri, A. Meryandini, Yopi","doi":"10.5398/MEDPET.2014.37.3.190","DOIUrl":null,"url":null,"abstract":"Porang ( Amorphophallus muelleri Blume) is an indigenous Indonesian plant containing high hemicellulose as a source of glucomannan. An alternative way to produce a good quality of mannooligosaccharides was through hydrolysis of glucomannan by endo-β mannnase from actynomicetes. Based on 16S rRNA analysis, BF 3.10 isolate, isolated from Bukit Duabelas National Park soil, Jambi was identified as Streptomyces violascens BF 3.10 . Reducing sugar was analyzed by dinitrosalicylic acid methods. The highest reducing sugar was achieved at the 72 hours of incubation. Mannanase of isolate BF 3.10 had the highest activity at pH 6 and temperature of 70 °C with enzyme activity of 16.38 U/mL and was stable at 4 °C for 48 h. During 5-hour of hydrolysis with substrate concentration of 0.25%, 0.5%, and 1% porang glucomannan dissolved in 10 mL enzyme, mannooligosaccharides were produced with the degree of polymerization of 2-3. Visualization of the products by using thin layer chromatography (TLC) and high performance liquid chromatography (HPLC) methods showed that mannooligosaccharides produced comprised of glucose, mannobiose, mannotriose, and mannotetraose. The degree of polymerization and the simple sugars produced indicated that mannanase produced by S. violascens actively catalyzed the hydrolysis of 1.4-β-D-mannoside linkage from β-1.4-mannan backbone, that eventually produced simple sugars of mannooligosaccharides. Key words: glucomannan, mannanase, mannooligosaccharides, porang, Streptomyces violascens","PeriodicalId":18346,"journal":{"name":"Media Peternakan","volume":"37 1","pages":"190-197"},"PeriodicalIF":0.0000,"publicationDate":"2014-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.5398/MEDPET.2014.37.3.190","citationCount":"7","resultStr":"{\"title\":\"Enzymatic Hydrolysis of Porang by Streptomyces violascens BF 3.10 Mannanase for the Production of Mannooligosaccharides\",\"authors\":\"A. Safitri, A. Meryandini, Yopi\",\"doi\":\"10.5398/MEDPET.2014.37.3.190\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Porang ( Amorphophallus muelleri Blume) is an indigenous Indonesian plant containing high hemicellulose as a source of glucomannan. An alternative way to produce a good quality of mannooligosaccharides was through hydrolysis of glucomannan by endo-β mannnase from actynomicetes. Based on 16S rRNA analysis, BF 3.10 isolate, isolated from Bukit Duabelas National Park soil, Jambi was identified as Streptomyces violascens BF 3.10 . Reducing sugar was analyzed by dinitrosalicylic acid methods. The highest reducing sugar was achieved at the 72 hours of incubation. Mannanase of isolate BF 3.10 had the highest activity at pH 6 and temperature of 70 °C with enzyme activity of 16.38 U/mL and was stable at 4 °C for 48 h. During 5-hour of hydrolysis with substrate concentration of 0.25%, 0.5%, and 1% porang glucomannan dissolved in 10 mL enzyme, mannooligosaccharides were produced with the degree of polymerization of 2-3. Visualization of the products by using thin layer chromatography (TLC) and high performance liquid chromatography (HPLC) methods showed that mannooligosaccharides produced comprised of glucose, mannobiose, mannotriose, and mannotetraose. The degree of polymerization and the simple sugars produced indicated that mannanase produced by S. violascens actively catalyzed the hydrolysis of 1.4-β-D-mannoside linkage from β-1.4-mannan backbone, that eventually produced simple sugars of mannooligosaccharides. Key words: glucomannan, mannanase, mannooligosaccharides, porang, Streptomyces violascens\",\"PeriodicalId\":18346,\"journal\":{\"name\":\"Media Peternakan\",\"volume\":\"37 1\",\"pages\":\"190-197\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-12-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.5398/MEDPET.2014.37.3.190\",\"citationCount\":\"7\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Media Peternakan\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5398/MEDPET.2014.37.3.190\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Media Peternakan","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5398/MEDPET.2014.37.3.190","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7
摘要
Porang (Amorphophallus muelleri Blume)是一种印尼本土植物,含有高半纤维素作为葡甘露聚糖的来源。另一种生产优质甘露寡糖的方法是利用产自活动菌的内切-β甘露聚糖酶水解葡甘露聚糖。基于16S rRNA分析,从武吉杜阿贝拉国家公园(Bukit Duabelas National Park, Jambi)土壤中分离到的BF 3.10菌株为violascens Streptomyces BF 3.10。用二硝基水杨酸法分析还原糖。在孵育72小时时,还原糖达到最高。菌株BF 3.10的甘露聚糖酶在pH 6、温度70℃条件下活性最高,酶活性为16.38 U/mL,在4℃条件下可稳定水解48 h。在10 mL酶中分别以0.25%、0.5%和1%葡甘露聚糖的底物浓度水解5 h,可制得2 ~ 3度的甘露聚糖。通过薄层色谱(TLC)和高效液相色谱(HPLC)对产物进行可视化分析,得到的甘露寡糖主要由葡萄糖、甘露糖、甘露糖和甘露糖组成。聚合程度和产生的单糖表明,紫花葡萄产生的甘露聚糖酶能催化β-1.4- β- d -甘露聚糖键水解,最终产生甘露寡糖单糖。关键词:葡甘露聚糖,甘露聚糖酶,甘露寡糖,porang,紫链霉菌
Enzymatic Hydrolysis of Porang by Streptomyces violascens BF 3.10 Mannanase for the Production of Mannooligosaccharides
Porang ( Amorphophallus muelleri Blume) is an indigenous Indonesian plant containing high hemicellulose as a source of glucomannan. An alternative way to produce a good quality of mannooligosaccharides was through hydrolysis of glucomannan by endo-β mannnase from actynomicetes. Based on 16S rRNA analysis, BF 3.10 isolate, isolated from Bukit Duabelas National Park soil, Jambi was identified as Streptomyces violascens BF 3.10 . Reducing sugar was analyzed by dinitrosalicylic acid methods. The highest reducing sugar was achieved at the 72 hours of incubation. Mannanase of isolate BF 3.10 had the highest activity at pH 6 and temperature of 70 °C with enzyme activity of 16.38 U/mL and was stable at 4 °C for 48 h. During 5-hour of hydrolysis with substrate concentration of 0.25%, 0.5%, and 1% porang glucomannan dissolved in 10 mL enzyme, mannooligosaccharides were produced with the degree of polymerization of 2-3. Visualization of the products by using thin layer chromatography (TLC) and high performance liquid chromatography (HPLC) methods showed that mannooligosaccharides produced comprised of glucose, mannobiose, mannotriose, and mannotetraose. The degree of polymerization and the simple sugars produced indicated that mannanase produced by S. violascens actively catalyzed the hydrolysis of 1.4-β-D-mannoside linkage from β-1.4-mannan backbone, that eventually produced simple sugars of mannooligosaccharides. Key words: glucomannan, mannanase, mannooligosaccharides, porang, Streptomyces violascens