• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Strain improvement of Aspergillus niger for the enhanced production of asperenone.黑曲霉的菌株改良以提高asperenone 的产量。
Indian J Microbiol. 2008 Jun;48(2):274-8. doi: 10.1007/s12088-008-0026-1. Epub 2008 Jun 13.
2
Strain improvement of Aspergillus niger for enhanced lipase production.黑曲霉的菌株改良以提高脂肪酶产量。
J Gen Appl Microbiol. 2001 Aug;47(4):181-186. doi: 10.2323/jgam.47.181.
3
Mutagenesis and analysis of mold Aspergillus niger for extracellular glucose oxidase production using sugarcane molasses.利用甘蔗废蜜对黑曲霉进行诱变及胞外葡萄糖氧化酶生产分析。
Appl Biochem Biotechnol. 2006 Oct;135(1):43-57. doi: 10.1385/abab:135:1:43.
4
Screening and mutagenesis of Aspergillus niger for the improvement of glucose 6-phosphate dehydrogenase production.黑曲霉的筛选与诱变以提高6-磷酸葡萄糖脱氢酶的产量
Prikl Biokhim Mikrobiol. 2003 Sep-Oct;39(5):561-4.
5
Gluconic acid production by Aspergillus niger mutant ORS-4.410 in submerged and solid state surface fermentation.黑曲霉突变体ORS-4.410在深层发酵和固态表面发酵中生产葡萄糖酸
Indian J Exp Biol. 2001 Jul;39(7):691-6.
6
Enhancement of epoxide hydrolase production by Co gamma and UV irradiation mutagenesis of Aspergillus niger ZJB-09103.
Biotechnol Appl Biochem. 2017 May;64(3):392-399. doi: 10.1002/bab.1502. Epub 2016 Dec 15.
7
Citric acid production by selected mutants of Aspergillus niger from cane molasses.利用甘蔗废蜜筛选出的黑曲霉突变体生产柠檬酸
Bioresour Technol. 2004 Jun;93(2):125-30. doi: 10.1016/j.biortech.2003.10.018.
8
Citric Acid Production from Acorn Starch by Tannin Tolerance Mutant Aspergillus niger AA120.栎仁淀粉柠檬酸生产黑曲霉单宁耐性突变株 AA120。
Appl Biochem Biotechnol. 2019 May;188(1):1-11. doi: 10.1007/s12010-018-2902-4. Epub 2018 Oct 3.
9
Citric acid production by a novel Aspergillus niger isolate: I. Mutagenesis and cost reduction studies.新型黑曲霉分离株产柠檬酸:I. 诱变及成本降低研究
Bioresour Technol. 2007 Dec;98(18):3464-9. doi: 10.1016/j.biortech.2006.11.007. Epub 2007 Jan 12.
10
Effect of branch frequency in Aspergillus oryzae on protein secretion and culture viscosity.米曲霉分支频率对蛋白质分泌及培养物粘度的影响。
Biotechnol Bioeng. 1999 Dec 20;65(6):638-48. doi: 10.1002/(sici)1097-0290(19991220)65:6<638::aid-bit4>3.0.co;2-k.

引用本文的文献

1
as a Secondary Metabolite Factory.作为一个次生代谢产物工厂。
Front Chem. 2021 Jul 30;9:701022. doi: 10.3389/fchem.2021.701022. eCollection 2021.
2
Safety of the fungal workhorses of industrial biotechnology: update on the mycotoxin and secondary metabolite potential of Aspergillus niger, Aspergillus oryzae, and Trichoderma reesei.工业生物技术中真菌“工作伙伴”的安全性:黑曲霉、米曲霉和里氏木霉的真菌毒素和次生代谢产物潜力的最新研究进展。
Appl Microbiol Biotechnol. 2018 Nov;102(22):9481-9515. doi: 10.1007/s00253-018-9354-1. Epub 2018 Oct 6.

本文引用的文献

1
Strain improvement of Aspergillus niger for enhanced lipase production.黑曲霉的菌株改良以提高脂肪酶产量。
J Gen Appl Microbiol. 2001 Aug;47(4):181-186. doi: 10.2323/jgam.47.181.
2
Nigerloxin, a novel inhibitor of aldose reductase and lipoxygenase with Free radical scavenging activity from Aspergillus niger CFR-W-105.黑曲霉毒素,一种来自黑曲霉CFR-W-105的具有自由基清除活性的新型醛糖还原酶和脂氧合酶抑制剂。
J Antibiot (Tokyo). 2002 Sep;55(9):789-93. doi: 10.7164/antibiotics.55.789.
3
A lipoxygenase inhibitor from Aspergillus niger.一种来自黑曲霉的脂氧合酶抑制剂。
Appl Microbiol Biotechnol. 2002 Mar;58(4):539-42. doi: 10.1007/s00253-001-0913-4.
4
At last, direct evidence that lipoxygenases play a role in atherogenesis.最后,有直接证据表明脂氧合酶在动脉粥样硬化形成过程中发挥作用。
J Clin Invest. 1999 Jun;103(11):1487-8. doi: 10.1172/JCI7298.
5
15-Lipoxygenase and its inhibition: a novel therapeutic target for vascular disease.15-脂氧合酶及其抑制作用:血管疾病的新型治疗靶点。
Curr Pharm Des. 1999 Jan;5(1):11-20.
6
Structure and mechanism of lipoxygenases.脂氧合酶的结构与作用机制。
Biochimie. 1997 Nov;79(11):629-36. doi: 10.1016/s0300-9084(97)83495-5.
7
Steroids and other factors influenceing the accumulation of asperenone and fermentation acids by Aspergillus niger in replacement cultures.
Biochemistry. 1967 Nov;6(11):3484-8. doi: 10.1021/bi00863a020.
8
The isolation and characterization of asperenone, a new phenylpolyene from Aspergillus niger.
Biochemistry. 1967 Nov;6(11):3479-84. doi: 10.1021/bi00863a019.
9
Three methods of assessing the mutagenic action of ultraviolet radiation on the fungus Emericellopsis glabra.评估紫外线对光滑埃默森霉的诱变作用的三种方法。
Appl Microbiol. 1966 Jan;14(1):105-9. doi: 10.1128/am.14.1.105-109.1966.
10
Enzymology and physiology of reticulocyte lipoxygenase: comparison with other lipoxygenases.网织红细胞脂氧合酶的酶学与生理学:与其他脂氧合酶的比较。
Adv Enzymol Relat Areas Mol Biol. 1986;58:191-272. doi: 10.1002/9780470123041.ch6.

黑曲霉的菌株改良以提高asperenone 的产量。

Strain improvement of Aspergillus niger for the enhanced production of asperenone.

机构信息

Fermentation Technology and Bioengineering Department, Central Food Technological Research Institute, Mysore, 570 013 India.

出版信息

Indian J Microbiol. 2008 Jun;48(2):274-8. doi: 10.1007/s12088-008-0026-1. Epub 2008 Jun 13.

DOI:10.1007/s12088-008-0026-1
PMID:23100720
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3450179/
Abstract

The enhancement of production of asperenone (Fig. 1), an inhibitor of lipoxygenase and human platelet aggregation from Aspergillus niger CFTRI 1105, was achieved by UV and nitrous acid mutagenesis. Nitrous acid mutants exhibited increased inhibitor production when compared with UV irradiated mutants. I N 41 a first-generation nitrous acid mutant produced 5.1 fold increased asperenone over parent strain. Mutant II N 31 obtained by second-generation nitrous acid treatment produced 60.3 mg asperenone/g biomass, which was 131 fold increase when compared to first generated mutant I N 41 and 670 fold increase over the parent strain. This mutant was stable for several generations on production medium.

摘要

通过 UV 和亚硝酸诱变,提高了黑曲霉 CFTRI 1105 中脂氧合酶和人血小板聚集抑制剂 Asperenone(图 1)的产量。与 UV 照射突变体相比,亚硝酸突变体表现出更高的抑制剂产量。第一代亚硝酸突变体 IN 41 的 Asperenone 产量比亲本菌株提高了 5.1 倍。通过第二代亚硝酸处理得到的突变体 II N 31 产生 60.3mg Asperenone/g 生物质,与第一代突变体 IN 41 相比提高了 131 倍,与亲本菌株相比提高了 670 倍。该突变体在生产培养基中连续几代都很稳定。