从泥土到链霉菌DNA

CourseSource Pub Date : 2021-01-01 DOI:10.24918/cs.2021.32
M. Brodkin
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The blastn program provides the final piece of evidence used to confirm, or not, the identification of their isolate as a Streptomyces from 16s rRNA gene sequence data, hence the title “From Dirt to Streptomyces DNA. In addition, the Lesson focuses on the Streptomyces bacteria to address several ASM aligned goals and objectives. These include prokaryotic growth phases and ways in which interactions of microorganisms among themselves and with their environment is determined by their metabolic abilities. In addition, this Lesson illustrates how microbial metabolism is important to a relevant societal issue, the need for new antibiotic discovery particularly given the rise of antibiotic resistance strains of clinically relevant bacteria. It also illustrates the microbial diversity of soil and the developmental/physiological strategies employed in such a competitive environment. This Lesson hopes to impart both the thrill and challenges associated with scientific discovery. 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Conflict of Interest and Funding Statement: The Widener University Provost Grant Program supported part of this work. The author does not have a financial, personal, or professional conflict of interest related to this work. Supporting Materials: Supporting Files S1. Dirt to DNA-Handout Introduction to the Actinobacteria (LAB 1); S2. Dirt to DNA-Handout Serial dilution and spread plate technique (LAB 2); S3. Dirt to DNA-Handout Count serial dilution plates and subculture to ISP medium 2 (LAB 3); S4. Dirt to DNA-Handout slide culture technique (LAB 5); S5. Dirt to DNA-Handout Check pure culture isolates for antibiotic action (LAB 6); S6. Dirt to DNA-Handout Grow suspected Streptomyces isolates in broth culture (LAB 7); S7. Dirt to DNA-Handout DNA extraction from broth culture of Streptomyces isolate (LAB 8); S8. Dirt to DNA-Handout Agarose gel electrophoresis of DNA extraction and UV scan (LAB 9); S9. Dirt to DNA-Handout Polymerase Chain Reaction (LAB 10); S10. 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引用次数: 0

摘要

本学期课程的目的是给学生一个真实的,基于课程的本科研究经验,在此期间他们学习基本和高级微生物和分子生物学技术。本项目首先从土壤样本中分离出一种疑似链霉菌,最后对其进行鉴定。学生收集关于菌落和细胞形态、生化特征、次生代谢物产生的数据,并使用定制设计的引物对链霉菌16s rRNA基因进行PCR。该项目最终通过使用国家生物技术信息中心(NCBI)网站进行核苷酸爆炸来鉴定他们的土壤分离物。从16s rRNA基因序列数据来看,胚程序提供了最后的证据,用于确认或不确定他们的分离物是否为链霉菌,因此标题为“从污垢到链霉菌DNA”。此外,课程着重于链霉菌细菌,以解决几个ASM一致的目标和目的。这些包括原核生物的生长阶段和微生物之间以及与环境的相互作用由其代谢能力决定的方式。此外,本课还说明了微生物代谢对相关社会问题的重要性,特别是考虑到临床相关细菌的抗生素耐药菌株的增加,需要发现新的抗生素。它还说明了土壤微生物的多样性和在这种竞争环境中采用的发育/生理策略。本课希望传授与科学发现相关的刺激和挑战。引用本文:Brodkin MA。2021. 从泥土到链霉菌的DNA。CourseSource。https://doi.org/10.24918/cs.2021.32编辑:Rachel Horak,美国微生物学会收稿日期:1/9/2020;接受:4/30/2021;出版日期:2021年10月25日版权:©2021 Brodkin。这是一篇在知识共享署名-非商业-相同方式共享4.0国际许可协议下发布的开放获取文章,该协议允许在任何媒体上不受限制的非商业使用、分发和复制,前提是要注明原作者和来源。Bio-Protocol LLC已通过电子邮件书面许可在LAB 8 (S7)中使用协议。Qiagen已通过书面图像转让协议授权在LAB 8 (S7)中使用其协议。Genewiz.com已经通过电子邮件给予书面许可,在LAB 11(S10)中使用他们网站的屏幕截图。NCBI NBLAST网站是一个开源网站。利益冲突和资金声明:威德纳大学教务长资助计划支持了部分工作。作者没有与本工作相关的财务、个人或专业利益冲突。支持材料:支持文件从污垢到dna——放线菌介绍(LAB 1)S2。污垢DNA-Handout系列稀释扩散板技术(lab2)S3。污垢到DNA-Handout计数系列稀释板和传代到ISP培养基2 (LAB 3);S4。污垢到dna -讲义玻片培养技术(LAB 5);S5。检测纯培养分离物的抗生素作用(LAB 6);S6。在肉汤培养中培养可疑链霉菌(lab7)S7。从链霉菌分离菌肉汤培养物(lab8)中提取DNAS8。污垢到DNA- handout琼脂糖凝胶电泳的DNA提取和紫外扫描(lab9)S9。污垢到dna的聚合酶链反应(lab10)S10。Dirt to dna - Genewiz.com上16s rRNA基因的handout PCR产物测序(LAB 11)S11系列。污垢dna -讲义*NCBI核苷酸Blast (blastn) (LAB 12);S12。污垢到dna -分发实验室报告大纲(LAB 13);向。污垢dna -细菌培养,培养基,溶液配方和设备;S14系列。污垢到DNA-DNA提取协议指导复制;和S15。污垢dna -学生支持文件实验室1-12。*通讯:Marc Brodkin。怀德纳大学生物系,宾夕法尼亚州切斯特市大学广场1号,19013。电子邮件:brodkinmarc22616@gmail.com CourseSource | www.coursesource.org 2021 |卷08 1课
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Dirt to Streptomyces DNA
The purpose of this semester-long Lesson is to give students an authentic, course-based undergraduate research experience during which they learn basic and advanced microbiological and molecular biology techniques. This project begins with the isolation of a suspected Streptomyces bacterium from a soil sample and concludes with its identification. Students collect data, regarding colony and cell morphology, biochemical characteristics, the production of secondary metabolites, and employs the PCR using custom-designed primers to the Streptomyces 16s rRNA gene. The project culminates with the identification of their soil isolate using the National Center for Biotechnology Information (NCBI) web site to perform nucleotide blasts. The blastn program provides the final piece of evidence used to confirm, or not, the identification of their isolate as a Streptomyces from 16s rRNA gene sequence data, hence the title “From Dirt to Streptomyces DNA. In addition, the Lesson focuses on the Streptomyces bacteria to address several ASM aligned goals and objectives. These include prokaryotic growth phases and ways in which interactions of microorganisms among themselves and with their environment is determined by their metabolic abilities. In addition, this Lesson illustrates how microbial metabolism is important to a relevant societal issue, the need for new antibiotic discovery particularly given the rise of antibiotic resistance strains of clinically relevant bacteria. It also illustrates the microbial diversity of soil and the developmental/physiological strategies employed in such a competitive environment. This Lesson hopes to impart both the thrill and challenges associated with scientific discovery. Citation: Brodkin MA. 2021. From dirt to Streptomyces DNA. CourseSource. https://doi.org/10.24918/cs.2021.32 Editor: Rachel Horak, American Society for Microbiology Received: 1/9/2020; Accepted: 4/30/2021; Published: 10/25/2021 Copyright: © 2021 Brodkin. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. Bio-Protocol LLC has given written permission via email for protocol use in LAB 8 (S7). Qiagen has granted permission to use their protocol in LAB 8 (S7) with a written Image Transfer Agreement. Genewiz.com has given written permission via email to use screen shots from their web site in LAB 11(S10). NCBI NBLAST site is an open-source web site. Conflict of Interest and Funding Statement: The Widener University Provost Grant Program supported part of this work. The author does not have a financial, personal, or professional conflict of interest related to this work. Supporting Materials: Supporting Files S1. Dirt to DNA-Handout Introduction to the Actinobacteria (LAB 1); S2. Dirt to DNA-Handout Serial dilution and spread plate technique (LAB 2); S3. Dirt to DNA-Handout Count serial dilution plates and subculture to ISP medium 2 (LAB 3); S4. Dirt to DNA-Handout slide culture technique (LAB 5); S5. Dirt to DNA-Handout Check pure culture isolates for antibiotic action (LAB 6); S6. Dirt to DNA-Handout Grow suspected Streptomyces isolates in broth culture (LAB 7); S7. Dirt to DNA-Handout DNA extraction from broth culture of Streptomyces isolate (LAB 8); S8. Dirt to DNA-Handout Agarose gel electrophoresis of DNA extraction and UV scan (LAB 9); S9. Dirt to DNA-Handout Polymerase Chain Reaction (LAB 10); S10. Dirt to DNA-Handout PCR Product Sequencing of 16s rRNA gene at Genewiz.com (LAB 11); S11. Dirt to DNA-Handout *NCBI Nucleotide Blast (blastn) (LAB 12); S12. Dirt to DNA-Handout Laboratory Report Outline (LAB 13); S13. Dirt to DNA-Bacterial cultures, Media, Solution recipes, and Equipment; S14. Dirt to DNA-DNA extraction protocols instructor copy; and S15. Dirt to DNA-Student Supporting Files LAB 1-12. *Correspondence to: Marc Brodkin. Widener University, Department of Biology, One University Place, Chester, PA 19013. Email: brodkinmarc22616@gmail.com CourseSource | www.coursesource.org 2021 | Volume 08 1 Lesson
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