Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Outer Layers of the Cell Envelope01:18

Outer Layers of the Cell Envelope

1.1K
The outermost layers of prokaryotic cells play a critical role in their survival, virulence, and interaction with the environment. These layers, often composed of polysaccharides, polypeptides, or proteins, form protective and adhesive structures that vary in organization and function.Capsules and Slime LayersCapsules are highly organized, tightly bound layers that firmly attach to the bacterial cell wall. Capsules are usually made of polysaccharides, though some are made of polypeptides. These...
1.1K
Bacterial Cell Wall01:22

Bacterial Cell Wall

3.4K
The bacterial cell wall is an essential structural component that encases the plasma membrane, preserving cellular integrity, determining shape, and protecting against osmotic stress. This rigid yet flexible structure primarily comprises peptidoglycan, a polymer that forms a mesh-like matrix conferring mechanical strength and flexibility.Peptidoglycan Composition and StructurePeptidoglycan, the core of the bacterial cell wall, comprises alternating units of N-acetylglucosamine (NAG) and...
3.4K
Bacterial Transformation01:33

Bacterial Transformation

60.1K
In 1928, bacteriologist Frederick Griffith worked on a vaccine for pneumonia, which is caused by Streptococcus pneumoniae bacteria. Griffith studied two pneumonia strains in mice: one pathogenic and one non-pathogenic. Only the pathogenic strain killed host mice.
Griffith made an unexpected discovery when he killed the pathogenic strain and mixed its remains with the live, non-pathogenic strain. Not only did the mixture kill host mice, but it also contained living pathogenic bacteria that...
60.1K
Bacterial Signaling01:30

Bacterial Signaling

40.8K
Bacterial signaling can occur within bacteria (intracellular) or between bacteria (intercellular). At times, a group of bacteria behaves like a community. To achieve this, they engage in quorum sensing, the perception of higher cell density that causes changes in gene expression. Quorum sensing involves both extracellular and intracellular signaling. The signaling cascade starts with a molecule called an autoinducer (AI). Individual bacteria produce AIs that move out of the bacterial cell...
40.8K
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

32.8K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
32.8K
Bacterial Transcription01:53

Bacterial Transcription

36.6K
RNA polymerase (RNAP) carries out DNA-dependent RNA synthesis in both bacteria and eukaryotes. Bacteria do not have a membrane-bound nucleus. So, transcription and translation occur simultaneously, on the same DNA template.
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
36.6K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Reply to the letter regarding 'Unravelling the genomic landscape of Canadian <i>Borrelia burgdorferi</i>'.

Microbial genomics·2026
Same author

HER2-driven mammary tumorigenesis enhances bioenergetics despite reductions in mitochondrial content.

eLife·2026
Same author

Automated detection of superior mesenteric artery occlusion on post-contrast CT Using a 3D deep learning model.

Clinical imaging·2026
Same author

Unravelling the genomic landscape of Canadian <i>Borrelia burgdorferi</i>: a comparison across global strains.

Microbial genomics·2026
Same author

OMIP-119: A 36-Color Full-Spectrum Flow Cytometry Panel for Deep Immunophenotyping of Peripheral Blood and Ex Vivo Expanded Human T Cells.

Cytometry. Part A : the journal of the International Society for Analytical Cytology·2025
Same author

Dr. Robert Murray: strong roots in Canadian microbiology-strong global leadership and vision.

Canadian journal of microbiology·2025

Related Experiment Video

Updated: Feb 5, 2026

Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay
07:10

Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay

Published on: September 14, 2014

14.7K

Inroads through the bacterial cell envelope: seeing is believing.

Cezar M Khursigara1,2, Susan F Koval3, Dianne M Moyles2

  • 1a Department of Molecular and Cellular Biology, University of Guelph, Guelph, ON N1G 2W1, Canada.

Canadian Journal of Microbiology
|September 1, 2018
PubMed
Summary

This review highlights Terry Beveridge's pioneering work on bacterial cell envelopes and surface layers (S-layers). His research advanced cryo-electron microscopy techniques, revealing bacterial ultrastructure and assembly processes.

Keywords:
CEMOVISTerry J. Beveridgecell envelopecouches de surfacecryo-electron microscopycryomicroscopie électroniqueenveloppe cellulairesurface layers

More Related Videos

Separation of the Cell Envelope for Gram-negative Bacteria into Inner and Outer Membrane Fractions with Technical Adjustments for Acinetobacter baumannii
10:24

Separation of the Cell Envelope for Gram-negative Bacteria into Inner and Outer Membrane Fractions with Technical Adjustments for Acinetobacter baumannii

Published on: April 10, 2020

14.4K
Determination of Molecular Structures of HIV Envelope Glycoproteins using Cryo-Electron Tomography and Automated Sub-tomogram Averaging
07:29

Determination of Molecular Structures of HIV Envelope Glycoproteins using Cryo-Electron Tomography and Automated Sub-tomogram Averaging

Published on: December 1, 2011

42.0K

Related Experiment Videos

Last Updated: Feb 5, 2026

Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay
07:10

Conformational Evaluation of HIV-1 Trimeric Envelope Glycoproteins Using a Cell-based ELISA Assay

Published on: September 14, 2014

14.7K
Separation of the Cell Envelope for Gram-negative Bacteria into Inner and Outer Membrane Fractions with Technical Adjustments for Acinetobacter baumannii
10:24

Separation of the Cell Envelope for Gram-negative Bacteria into Inner and Outer Membrane Fractions with Technical Adjustments for Acinetobacter baumannii

Published on: April 10, 2020

14.4K
Determination of Molecular Structures of HIV Envelope Glycoproteins using Cryo-Electron Tomography and Automated Sub-tomogram Averaging
07:29

Determination of Molecular Structures of HIV Envelope Glycoproteins using Cryo-Electron Tomography and Automated Sub-tomogram Averaging

Published on: December 1, 2011

42.0K

Area of Science:

  • Microbiology
  • Cell Biology
  • Biophysics

Background:

  • Prokaryotic cells possess a unique cell envelope comprising a cytoplasmic membrane and cell wall.
  • Bacterial cell fractionation and electron microscopy advancements in the mid-20th century enabled detailed cell envelope studies.

Purpose of the Study:

  • To review Terry Beveridge's significant contributions to understanding bacterial cell envelope structure and ultrastructure.
  • To highlight the impact of cryo-electron microscopy techniques developed and applied by Beveridge.

Main Methods:

  • Review of historical research and publications by Terry Beveridge.
  • Exploration of cryogenic methods for preserving bacterial ultrastructure.
  • Application of cryo-electron microscopy, including CEMOVIS, for imaging bacterial cell envelopes.

Main Results:

  • Beveridge's early work elucidated the structure of paracrystalline surface layers (S-layers).
  • Advancements in cryo-electron microscopy provided unprecedented insights into S-layer assembly and bacterial cell envelope ultrastructure.
  • CEMOVIS enabled visualization of the Gram-positive cell envelope.

Conclusions:

  • Terry Beveridge made seminal contributions to bacterial cell envelope research through innovative microscopy techniques.
  • His work significantly advanced the understanding of S-layer structure, assembly, and the overall ultrastructure of prokaryotic cell envelopes.