• [email protected]
  • +971 507 888 742
Submit Manuscript
SciAlert
  • Home
  • Journals
  • Information
    • For Authors
    • For Referees
    • For Librarian
    • For Societies
  • Contact
  1. Research Journal of Microbiology
  2. Vol 10 (7), 2015
  3. 329-335
  • Online First
  • Current Issue
  • Previous Issues
  • More Information
    Aims and Scope Editorial Board Guide to Authors Article Processing Charges
    Submit a Manuscript

Research Journal of Microbiology

Year: 2015 | Volume: 10 | Issue: 7 | Page No.: 329-335

Facebook Twitter Digg Reddit Linkedin StumbleUpon E-mail

Article Trend



Total views 369

Search


Authors


Ting He

Country: China

Linfang Li

Country: China

Jia Feng

Country: China

Haiqing Yu

Country: China

Keywords


  • Cas9 gene
  • Listeria innocua
  • gram-positive bacteria
  • quantitative real-time PCR
Research Article

Establishment of Quantitative Real-Time PCR System for Analyzing Cas9 Gene Expression in Listeria innocua

Ting He, Linfang Li, Jia Feng and Haiqing Yu
Currently, little is known about a protocol in establishing the quantitative Real-Time PCR (qRT-PCR) system in gram-positive bacteria. Also, it is obscure whether the expression level of clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (Cas9) in Listeria innocua is influenced by the pH. This study focused on providing a protocol for analyzing Cas9 gene expression in L. innocua at two pH conditions. The 37°C overnight culture was diluted 1:500 and grown in fresh Todd Hewitt Yeast extraction broth (THY) for 3 h. The collected pellet was washed two times in pH = 7.5 medium and was cultured for 4 h by using pH = 7.5 and pH = 6.0 medium, respectively. The culture was treated with RNA protection reagent for 5 min and the obtained pellet was suspended with mutanolysin for 30 min. Total RNA was extracted by using a kit and was incubated with DNase I, which was removed by adding phenol-chloroform-isoamyl alcohol thereafter. The purified RNA was precipitated via glycogen-ethanol treatment and was synthesized into cDNA. The 2‾ΔΔCt method was used to analyze the expression level of Cas9 gene with 16S rRNA gene as a reference. The gel electrophoresis showed that the quantity of 23S rRNA was about two-fold of 16S rRNA. The relative Cas9 expression levels of L. innocua in neutral and acidic medium were 1.08±0.49 and 1.66±0.54, respectively (p>0.05). Totally, the qRT-PCR system for analyzing Cas9 gene expression in L. innocua was successfully developed. The Cas9 expression level of L. innocua in acidic medium was similar to that in neutral medium.
PDF Fulltext XML References Citation

How to cite this article

Ting He, Linfang Li, Jia Feng and Haiqing Yu, 2015. Establishment of Quantitative Real-Time PCR System for Analyzing Cas9 Gene Expression in Listeria innocua. Research Journal of Microbiology, 10: 329-335.

URL: https://scialert.net/abstract/?doi=jm.2015.329.335

Leave a Comment


Your email address will not be published. Required fields are marked *

Useful Links

  • Journals
  • For Authors
  • For Referees
  • For Librarian
  • For Socities

Contact Us

Office Number 1128,
Tamani Arts Building,
Business Bay,
Deira, Dubai, UAE

Phone: +971 507 888 742
Email: [email protected]

About Science Alert

Science Alert is a technology platform and service provider for scholarly publishers, helping them to publish and distribute their content online. We provide a range of services, including hosting, design, and digital marketing, as well as analytics and other tools to help publishers understand their audience and optimize their content. Science Alert works with a wide variety of publishers, including academic societies, universities, and commercial publishers.

Follow Us
© Copyright Science Alert. All Rights Reserved