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Related Concept Videos

Diversity of Protists II01:27

Diversity of Protists II

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Alveolates are a group of organisms recognized by the presence of alveoli, which are cytoplasmic sacs located beneath the cell membrane. While their function remains uncertain, alveoli may help regulate water balance by controlling how much water enters and leaves the cell. In dinoflagellates, these structures may serve as armor plates. There are three major types of alveolates: ciliates, which move using cilia; dinoflagellates, which use flagella for movement; and apicomplexans, which are...
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The ciliary structures were first seen in 1647 by Antonie Leeuwenhoek while observing the protozoans. In lower organisms, these appendages are responsible for cell movement, while in higher organisms, these appendages help in the movement of the extracellular fluids within the body cavities.
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ATP-driven pumps, also known as transport ATPases, are integral membrane proteins. They have binding sites for ATP located on the membrane's cytosolic side and the ion-conducting domain in the transmembrane region. These pumps use the free energy released from ATP hydrolysis to move the solutes across cell membranes against an electrochemical gradient.
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Excavata is a diverse group of protists that includes both chemoorganotrophic and phototrophic species, with some thriving in anaerobic environments. Among the key groups within Excavata are diplomonads and parabasalids, which are flagellated protists that lack mitochondria and chloroplasts. These microorganisms typically inhabit anoxic environments, such as the intestines of animals, where they exist either symbiotically or as parasites, relying on fermentation for energy production. Some...
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Mitochondrial protein import is powered by two distinct energy sources: ATP hydrolysis and electrochemical potential across the inner membrane. Newly synthesized precursors are bound by cytosolic chaperones of the Hsp70 family, which guide them to the import receptors on the mitochondrial surface. Utilizing the energy of ATP hydrolysis, Hsp70 chaperones transfer these precursors to the TOM receptors on the mitochondrial outer membrane.
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Microorganisms rely on proteins as an essential carbon and energy source, particularly in environments with limited polysaccharides or lipids. However, proteins are too large to cross the plasma membrane unaided, necessitating enzymatic degradation. Microbes secrete extracellular proteases and peptidases that hydrolyze proteins into peptides, which can then be transported across the membrane. Once inside the cell, intracellular proteases degrade these peptides into free amino acids, which...
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Bioenergetic Profile Experiment using C2C12 Myoblast Cells
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Evolutionary bioenergetics of ciliates.

Michael Lynch1, Paul E Schavemaker1, Timothy J Licknack1

  • 1Biodesign Center for Mechanisms of Evolution, Arizona State University, Tempe, Arizona, USA.

The Journal of Eukaryotic Microbiology
|July 2, 2022
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Summary

Organisms evolve diverse lifestyles by balancing fitness benefits with cellular construction costs. This study quantizes cellular costs in ciliates, revealing how resource allocation scales with cell size.

Keywords:
ParameciumTetrahymenabioenergeticsciliatesevolutionary cell biologyosmoregulationribosomesswimming motility

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Area of Science:

  • Evolutionary biology
  • Cell biology
  • Bioenergetics

Background:

  • Ecological studies often focus on fitness advantages of phenotypic traits.
  • Resource allocation and cellular construction costs are understudied in evolutionary contexts.
  • Ciliates offer a diverse model for studying cellular investments.

Purpose of the Study:

  • To quantify the energetic costs of cellular structures and functions in ciliates.
  • To understand how these cellular costs scale with cell size.
  • To provide a framework for analyzing resource allocation in evolutionary bioenergetics.

Main Methods:

  • Utilized observations from diverse ciliate species.
  • Applied principles from evolutionary bioenergetics.
  • Developed a general estimator for cellular costs per cell cycle (ATP equivalents).

Main Results:

  • Provided a robust estimator for total cellular cost per cell cycle.
  • Analyzed scaling of investments in macronuclear genomes, ribosomes, membranes, osmoregulation, cilia, and motility with cell size.
  • Identified key cost drivers in ciliate cellular biology.

Conclusions:

  • Cellular construction and operating costs are critical factors in organismal evolution.
  • The developed bioenergetic framework can be extended to other traits and lineages.
  • Further research can refine understanding of resource allocation trade-offs.