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Metagenomic Approaches to Identify Novel Organisms from the Soil Environment in a Classroom Setting

机译:识别教室环境中土壤环境中新生物的元基因组学方法

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摘要

Molecular Microbial Metagenomics is a research-based undergraduate course developed at Georgia State University. This semester-long course provides hands-on research experience in the area of microbial diversity and introduces molecular approaches to study diversity. Students are part of an ongoing research project that uses metagenomic approaches to isolate clones containing 16S ribosomal ribonucleic acid (rRNA) genes from a soil metagenomic library. These approaches not only provide a measure of microbial diversity in the sample but may also allow discovery of novel organisms. Metagenomic approaches differ from the traditional culturing methods in that they use molecular analysis of community deoxyribonucleic acid (DNA) instead of culturing individual organisms. Groups of students select a batch of 100 clones from a metagenomic library. Using universal primers to amplify 16S rRNA genes from the pool of DNA isolated from 100 clones, and a stepwise process of elimination, each group isolates individual clones containing 16S rRNA genes within their batch of 100 clones. The amplified 16S rRNA genes are sequenced and analyzed using bioinformatics tools to determine whether the rRNA gene belongs to a novel organism. This course provides avenues for active learning and enhances students’ conceptual understanding of microbial diversity. Average scores on six assessment methods used during field testing indicated that success in achieving different learning objectives varied between 84% and 95%, with 65% of the students demonstrating complete grasp of the project based on the end-of-project lab report. The authentic research experience obtained in this course is also expected to result in more undergraduates choosing research-based graduate programs or careers.
机译:分子微生物元基因组学是乔治亚州立大学开发的基于研究的本科课程。这个为期一个学期的课程提供了微生物多样性领域的动手研究经验,并介绍了研究多样性的分子方法。学生是正在进行的研究项目的一部分,该项目使用宏基因组学方法从土壤宏基因组学文库中分离出包含16S核糖体核糖核酸(rRNA)基因的克隆。这些方法不仅可以测量样品中的微生物多样性,而且还可以发现新型生物。元基因组学方法与传统的培养方法不同之处在于,它们使用社区脱氧核糖核酸(DNA)的分子分析而不是培养单个生物。一群学生从宏基因组库中选择了100个克隆。使用通用引物从100个克隆中分离的DNA池中扩增16S rRNA基因,并逐步进行消除,每个小组在其100个克隆中分离出包含16S rRNA基因的单个克隆。使用生物信息学工具对扩增的16S rRNA基因进行测序和分析,以确定rRNA基因是否属于新型生物。该课程为积极学习提供了途径,并增强了学生对微生物多样性的概念性理解。在现场测试中使用的六种评估方法的平均分数表明,实现不同学习目标的成功率介于84%和95%之间,其中有65%的学生根据项目结束时的实验室报告表明对项目的完全掌握。通过本课程获得的真实研究经验也有望导致更多的本科生选择基于研究的研究生课程或职业。

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