Archaeal Nucleoid

The archaeal nucleoid is the non-membrane-bound region where an archaeal cell organizes and maintains its chromosome, coordinating genome storage with access to genetic information. Archaeal DNA is compacted through supercoiling and association with chromatin proteins, including archaeal histones and Alba, while topoisomerases adjust DNA topology during replication and transcription. Studying this organization reveals how genome structure functions in organisms that often inhabit extreme environments and share molecular features with both bacteria and eukaryotes. Research on archaeal nucleoids supports comparisons of chromosome biology, evolution, gene regulation, and adaptation to conditions such as high temperature, acidity, or salinity.

Archaeal Nucleoid - Related Videos

Education

JoVE Core - Microbiology

Nucleoid

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2025

The nucleoid represents a structurally and functionally distinct region within prokaryotic cells, where the cell's DNA and associated proteins are housed. Unlike eukaryotic cells, prokaryotes lack a membrane-bound nucleus, and the nucleoid facilitates the organization and accessibility of the genetic material within this constraint. The DNA in most bacteria and archaea exists as a single, circular, double-stranded molecule that is highly compacted through supercoiling and interactions with...

Archaeal Cell Wall

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2025

Archaeal cell walls are structurally and compositionally distinct from their bacterial counterparts, lacking the characteristic peptidoglycan layer found in most bacteria. Instead, archaeal cell walls exhibit remarkable diversity, utilizing materials such as pseudomurein, polysaccharides, and proteins to construct their protective outer layers. This structural flexibility is closely tied to archaea's ecological adaptability.S-Layers: The Common Archaeal Cell WallThe S-layer is the most...

Research

JoVE Journal - Biology

Specific Labeling of Mitochondrial Nucleoids for Time-lapse Structured Illumination Microscopy

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Cited by 2 •

2020

The protocol describes specific labeling of mitochondrial nucleoids with a commercially available DNA gel stain, acquisition of time lapse series of live labeled cells by super-resolution structured illumination microscopy (SR-SIM), and automatic tracking of nucleoid motion.

Examining Proteasome Assembly with Recombinant Archaeal Proteasomes and Nondenaturing PAGE: The Case for a Combined Approach

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Cited by 1 •

2016

This protocol uses both subunit coexpression and postlysis subunit mixing for a more thorough examination of recombinant proteasome assembly.

Microfluidic Time-Lapse Microscopy to Study Antibiotic Persistence in Bacteria

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2025

Source: Oms, T., et al. Population and Single-Cell Analysis of Antibiotic Persistence in Escherichia coli. J. Vis. Exp. (2023)This video presents a protocol for monitoring individual bacterial cells expressing a fluorescently labeled DNA-binding protein within a microfluidic system. It illustrates how antibiotics inhibit most cells, while a subpopulation of persister cells survives the treatment and regrows following antibiotic removal.

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