采用一次一个变量的方法改进新型埃祖鲁姆钙化杆菌 LEV207 的莱万生产。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Palkar Omkar Prakash, Keerthi Rayasam, Vidyullatha Peddireddy, Kolluru Viswanatha Chaitanya
{"title":"采用一次一个变量的方法改进新型埃祖鲁姆钙化杆菌 LEV207 的莱万生产。","authors":"Palkar Omkar Prakash, Keerthi Rayasam, Vidyullatha Peddireddy, Kolluru Viswanatha Chaitanya","doi":"10.1007/s10123-024-00597-5","DOIUrl":null,"url":null,"abstract":"<p><p>Levan, an exopolysaccharide, has applications in the medical and food sectors. Under natural conditions, levan is produced at a low concentration by microorganisms. This current study focuses on optimizing levan production by a one-variable-at-a-time approach from a novel marine bacterium, Calidifontibacillus erzurumensis LEV207. The growth and levansucrase production by C. erzurumensis LEV207 were studied to optimize the media components and conditions. Sucrose and yeast extract proved to be a good levansucrase inducer. The pH of 6.0 and temperature of 30 °C, along with MgSO<sub>4</sub> as salt, increased the enzyme activity. Sucrose and yeast extract at the concentration of 50% and 1%, respectively, produced the maximum enzyme activity of 427.4 µmol/mL/min after 48 h of incubation. Sevag reagent was used for the purification of levan. The optimization process increased the levan (EPSLEV207) production sevenfold with a final yield of 65.58 g/L. To confirm the structure and nature of EPSLEV207, NMR and XRD were performed, and the functional groups present in EPSLEV207 were determined using FTIR. Chemical hydrolysis of levan confirmed fructose as the monomer, making EPSLEV207 a homopolysaccharide. EPSLEV207 exhibited 49% and 22% radical scavenging activity against DPPH and ABTS radicals, respectively, and promoted the growth of probiotic strain. EPSLEV207 showed an 88% water solubility index and 78% water retention capacity. The optimization process has increased the yield of levan, highlighting the potential of C. erzurumensis LEV207 to be a viable option for industrial applications.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Improved levan production by novel Calidifontibacillus erzurumensis LEV207 using one variable at a time approach.\",\"authors\":\"Palkar Omkar Prakash, Keerthi Rayasam, Vidyullatha Peddireddy, Kolluru Viswanatha Chaitanya\",\"doi\":\"10.1007/s10123-024-00597-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Levan, an exopolysaccharide, has applications in the medical and food sectors. Under natural conditions, levan is produced at a low concentration by microorganisms. This current study focuses on optimizing levan production by a one-variable-at-a-time approach from a novel marine bacterium, Calidifontibacillus erzurumensis LEV207. The growth and levansucrase production by C. erzurumensis LEV207 were studied to optimize the media components and conditions. Sucrose and yeast extract proved to be a good levansucrase inducer. The pH of 6.0 and temperature of 30 °C, along with MgSO<sub>4</sub> as salt, increased the enzyme activity. Sucrose and yeast extract at the concentration of 50% and 1%, respectively, produced the maximum enzyme activity of 427.4 µmol/mL/min after 48 h of incubation. Sevag reagent was used for the purification of levan. The optimization process increased the levan (EPSLEV207) production sevenfold with a final yield of 65.58 g/L. To confirm the structure and nature of EPSLEV207, NMR and XRD were performed, and the functional groups present in EPSLEV207 were determined using FTIR. Chemical hydrolysis of levan confirmed fructose as the monomer, making EPSLEV207 a homopolysaccharide. EPSLEV207 exhibited 49% and 22% radical scavenging activity against DPPH and ABTS radicals, respectively, and promoted the growth of probiotic strain. EPSLEV207 showed an 88% water solubility index and 78% water retention capacity. The optimization process has increased the yield of levan, highlighting the potential of C. erzurumensis LEV207 to be a viable option for industrial applications.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-09-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s10123-024-00597-5\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10123-024-00597-5","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0

摘要

利凡(Levan)是一种外多糖,可应用于医疗和食品领域。在自然条件下,微生物可生产低浓度的莱万。本研究的重点是通过一种新型海洋细菌--Calidifontibacillus erzurumensis LEV207--的 "一次一变量 "方法优化利凡的生产。为了优化培养基成分和条件,对 C. erzurumensis LEV207 的生长和左旋琥珀酸酶的生产进行了研究。蔗糖和酵母提取物被证明是一种良好的左旋糖苷酶诱导剂。pH 值为 6.0、温度为 30 °C,并添加 MgSO4 作为盐,可提高酶的活性。蔗糖和酵母提取物的浓度分别为 50%和 1%,培养 48 小时后产生的最大酶活性为 427.4 µmol/mL/min。Sevag 试剂用于纯化 Levan。优化过程中,利凡(EPSLEV207)的产量提高了七倍,最终产量为 65.58 克/升。为了确认 EPSLEV207 的结构和性质,对其进行了核磁共振和 X 射线衍射,并利用傅立叶变换红外光谱测定了 EPSLEV207 中存在的官能团。化学水解利凡确认果糖为单体,从而使 EPSLEV207 成为一种均聚糖。EPSLEV207 对 DPPH 和 ABTS 自由基的清除活性分别为 49% 和 22%,并能促进益生菌株的生长。EPSLEV207 的水溶性指数为 88%,保水能力为 78%。优化过程提高了利凡的产量,凸显了 C. erzurumensis LEV207 在工业应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improved levan production by novel Calidifontibacillus erzurumensis LEV207 using one variable at a time approach.

Levan, an exopolysaccharide, has applications in the medical and food sectors. Under natural conditions, levan is produced at a low concentration by microorganisms. This current study focuses on optimizing levan production by a one-variable-at-a-time approach from a novel marine bacterium, Calidifontibacillus erzurumensis LEV207. The growth and levansucrase production by C. erzurumensis LEV207 were studied to optimize the media components and conditions. Sucrose and yeast extract proved to be a good levansucrase inducer. The pH of 6.0 and temperature of 30 °C, along with MgSO4 as salt, increased the enzyme activity. Sucrose and yeast extract at the concentration of 50% and 1%, respectively, produced the maximum enzyme activity of 427.4 µmol/mL/min after 48 h of incubation. Sevag reagent was used for the purification of levan. The optimization process increased the levan (EPSLEV207) production sevenfold with a final yield of 65.58 g/L. To confirm the structure and nature of EPSLEV207, NMR and XRD were performed, and the functional groups present in EPSLEV207 were determined using FTIR. Chemical hydrolysis of levan confirmed fructose as the monomer, making EPSLEV207 a homopolysaccharide. EPSLEV207 exhibited 49% and 22% radical scavenging activity against DPPH and ABTS radicals, respectively, and promoted the growth of probiotic strain. EPSLEV207 showed an 88% water solubility index and 78% water retention capacity. The optimization process has increased the yield of levan, highlighting the potential of C. erzurumensis LEV207 to be a viable option for industrial applications.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信