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A fundamental challenge in plant physiology is independently determining the rates of gross O production by photosynthesis and O consumption by respiration, photorespiration, and other processes. Previous studies on isolated chloroplasts or leaves have separately constrained net and gross O production (NOP and GOP, respectively) by labeling ambient O with O while leaf water was unlabeled. Here, we describe a method to accurately measure GOP and NOP of whole detached leaves in a cuvette as a routine gas-exchange measurement. The petiole is immersed in water enriched to a δO of ∼9,000‰, and leaf water is labeled through the transpiration stream. Photosynthesis transfers O from HO to O GOP is calculated from the increase in δO of O as air passes through the cuvette. NOP is determined from the increase in O/N Both terms are measured by isotope ratio mass spectrometry. CO assimilation and other standard gas-exchange parameters also were measured. Reproducible measurements are made on a single leaf for more than 15 h. We used this method to measure the light response curve of NOP and GOP in French bean () at 21% and 2% O We then used these data to examine the O/CO ratio of net photosynthesis, the light response curve of mesophyll conductance, and the apparent inhibition of respiration in the light (Kok effect) at both oxygen levels. The results are discussed in the context of evaluating the technique as a tool to study and understand leaf physiological traits.
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http://dx.doi.org/10.1104/pp.16.00741 | DOI Listing |
Mol Ther Methods Clin Dev
September 2025
Neuroscience Research Australia, Sydney, NSW 2031, Australia.
Optogenetics offers a minimally invasive, low-fatigue, and temporally precise alternative to electrical stimulation for skeletal muscle control. After opsin expression in muscle cells, contraction can be stimulated with light. Obstructive sleep apnea, characterized by repeated airway collapse during sleep, suits this approach, as upper airway muscles are readily accessible via the oral cavity, and require stimulation synchronized to respiration.
View Article and Find Full Text PDFCell Death Dis
September 2025
Department of Oncology, University of Oxford, Oxford, UK.
Iron is vital to living cells, playing a key role in cellular respiration, DNA synthesis, and various metabolic functions. Importantly, cancer cells have a higher dependency on iron compared to normal cells to support their rapid growth and survival. Due to this fact, tumors are more vulnerable to ferroptosis, an iron-dependent form of regulated cell death.
View Article and Find Full Text PDFBiosystems
October 2025
International Centre for Theoretical Sciences (ICTS), Tata Institute of Fundamental Research (TIFR), Bengaluru, India. Electronic address:
Cancer cells are often seen to prefer glycolytic metabolism over oxidative phosphorylation even in the presence of oxygen-a phenomenon termed the Warburg effect. Despite significant strides in the decades since its discovery, a clear basis is yet to be established for the Warburg effect and why cancer cells show such a preference for aerobic glycolysis. In this review, we draw on what is known about similar metabolic shifts both in normal mammalian physiology and overflow metabolism in microbes to shed new light on whether aerobic glycolysis in cancer represents some form of optimisation of cellular metabolism.
View Article and Find Full Text PDFPhysiol Plant
August 2025
Department of Botany, University of Innsbruck, Innsbruck, Austria.
Light and inorganic carbon (C) drive photosynthesis, which fuels cellular maintenance, energy storage, and growth in photosynthetic organisms. Despite its pivotal role, how primary metabolism adjusts to contrasting light and C availability in algae remains elusive. Here, we characterized bioenergetics and profiled primary metabolites of photoautotrophic Chlamydomonas reinhardtii cultures grown under constant low/sub-saturating (LL) or high/saturating (HL) light with 2% (CO) or ambient 0.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
CPCV, Département de chimie, École normale supérieure, PSL University, Sorbonne Université, CNRS, 24, rue Lhomond, Paris, 75005, France.
In cells, many small molecules are membrane-permeant. This feature opens a road to analyze their flux of production or consumption by quantitatively interpreting the map of their extracellular concentration within a reaction-diffusion frame. Here, this approach is implemented with a new wide-field lifetime imaging protocol applied to single microalgae cells sparsely deposited on an agarose pad loaded with a luminescent dioxygen (O) nanosensor.
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