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Systemic signaling and acclimation in response to excess excitation energy in Arabidopsis.

Land plants are sessile and have developed sophisticated mechanisms that allow for both immediate and acclimatory responses to changing environments. Partial exposure of low light-adapted Arabidopsis plants to excess light results in a systemic acclimation to excess excitation energy and consequent photooxidative stress in unexposed leaves. Thus, plants possess a mechanism to communicate excess excitation energy systemically, allowing them to mount a defense against further episodes of such stress. Systemic redox changes in the proximity of photosystem II, hydrogen peroxide, and the induction of antioxidant defenses are key determinants of this mechanism of systemic acquired acclimation.

Adaptation, Physiological↗

Methane production by fermentor cultures acclimated to waste from cattle fed monensin, lasalocid, salinomycin, or avoparcin.

The ability of microorganisms to ferment waste from cattle fed monensin, lasalocid, or salinomycin to methane was determined. Continuously mixed anaerobic fermentors with 3-liter working volumes at 55 degrees C were used; fermentors were fed once per day. Initially, all fermentors were fed waste without antibiotics at 6% volatile solids (VSs, organic matter) and a 20-day retention time (RT) for 60 days. Waste from animals fed monensin, lasalocid, or salinomycin at 29, 20, and 16.5 mg per kg of feed, respectively, was added to duplicate fermentors at the above VSs, and RT. Avoparcin (5 to 45 mg/liter) was not fed to animals but was added directly to duplicate fermentors. Lasalocid and salinomycin had minimal effects on the rate of methane production at RTs of 20 days and later at 6.5 days. Avoparcin caused an increase in organic acids from 599 to 1,672 mg/liter (as acetate) after 4 weeks, but by 6 weeks, acid concentrations declined and the rate of methane production was similar to controls at a 6.5-day RT. The monensin fermentors stopped producing methane 3 weeks after antibiotic addition. However, after a 6-month acclimation period, the microorganisms apparently adapted, and methane production rates of 1.65 and 2.51 liters per liter of fermentor volume per day were obtained with 6% VSs, and RTs of 10 and 6.5 days, respectively. This compares with 1.78 and 2.62 liters/liter per day for controls (P > 0.05). All fermentors that were fed waste containing antibiotics had lower pH values and ammonia and alkalinity concentrations, suggesting less buffering capacity and protein catabolism than in controls. Acclimation results obtained with fermentors at 35 degrees C were similar to those for fermentors at 55 degrees C. These studies indicate that waste from cattle fed these selected growth-promoting antibiotics can be thermophilically fermented to methane at RTs of 6.5 days or longer and VS concentrations of 6%, at rates comparable to waste without antibiotics.

Journal Article↗

Effects of Low-Temperature Acclimation and Oxygen Stress on Tocopheron Production in Euglena gracilis Z.

The effects of low-temperature acclimation and oxygen stress on tocopheron production were examined in the unicellular phytoflagellate Euglena gracilis Z. Cells were cultured photoheterotrophically at 27.5 +/- 1 degrees C with 5% carbon dioxide-95% air and 740 microeinsteins m s (photosynthetically active radiation) and served as controls. Low-temperature acclimation (12.5 +/- 1 degrees C) and high-oxygen stress (5% carbon dioxide-95% oxygen) were individually examined in the mass culturing of the algae. Chromatographic analyses demonstrated a six-to sevenfold enhancement of alpha-tocopherol production in temperature-stressed cells, along with a concomitant decline in the levels of alpha-tocotrienol and the absence of other tocopherol homologs. Oxygen-stressed cultures demonstrated the presence of high levels of alpha-tocopherylquinone; alpha-tocopheron and its homologs and precursors were absent or declined markedly. These findings are discussed in terms of the feasibility of microbial production of natural tocopherols. In addition, these results lend themselves to speculation regarding the biological role(s) of tocopherols as antioxidants and free radical scavengers in reducing photo-induced oxidative damage or lipid peroxidation toxicities or both in photosynthetically active E. gracilis Z.

Journal Article↗

Cold shock and cold acclimation proteins in the psychrotrophic bacterium Arthrobacter globiformis SI55.

The psychrotrophic bacterium Arthrobacter globiformis SI55 was grown at 4 and 25 degrees C, and the cell protein contents were analyzed by two-dimensional electrophoresis. Cells subjected to cold shocks of increasing magnitude were also analyzed. Correspondence analysis of protein appearance distinguished four groups of physiological significance. Group I contained cold shock proteins (Csps) overexpressed only after a large temperature downshift. Group II contained Csps with optimal expression after mild shocks. Group III contained proteins overexpressed after all cold shocks. These last proteins were also overexpressed in cells growing at 4 degrees C and were considered to be early cold acclimation proteins (Caps). Group IV contained proteins which were present at high concentrations only in 4 degrees C steady-state cells and appeared to be late Caps. A portion of a gene very similar to the Escherichia coli cspA gene (encoding protein CS7.4) was identified. A synthetic peptide was used to produce an antibody which detected a CS7.4-like protein (A9) by immunoblotting two-dimensional electrophoresis gels of A. globiformis SI55 total proteins. Unlike mesophilic microorganisms, this CS7.4-like protein was still produced during prolonged growth at low temperature, and it might have a particular adaptive function needed for balanced growth under harsh conditions. However, A9 was induced at high temperature by chloramphenicol, suggesting that CS7.4-like proteins have a more general role than their sole implication in cold acclimation processes.

Acclimatization↗

capA, a cspA-like gene that encodes a cold acclimation protein in the psychrotrophic bacterium Arthrobacter globiformis SI55.

By use of Arthrobacter globiformis SI55, a psychrotrophic bacterium capable of growth between -5 and +32 degrees C, we cloned and sequenced capA, a gene homologous to cspA encoding the major cold shock protein in Escherichia coli. The deduced protein sequence has a high level of identity with the sequences of other CspA-related proteins from various sources, and no particular residue or domain that could be specific to cold-adapted microorganisms emerged. We show that CapA was produced very rapidly following cold shock, but unlike its mesophilic counterparts, it was still expressed during prolonged growth at low temperature. Its synthesis is regulated at the translational level, and we showed that growth resumption following a temperature downshift correlated with CapA expression. Transient inhibitions in protein synthesis during the first stages of the cold shock response severely impaired the subsequent acclimation of A. globiformis SI55 to low temperature and delayed CapA expression. The cold shock response in A. globiformis SI55 is an adaptative process in which CapA may play a crucial role. We suggest that low-temperature acclimation is conditioned mainly by the ability of cells to restore an active translational machinery after cold shock in a process that may be different from that present in mesophiles.

Arthrobacter↗

Adaptation and acclimation of photosynthetic microorganisms to permanently cold environments.

Persistently cold environments constitute one of our world's largest ecosystems, and microorganisms dominate the biomass and metabolic activity in these extreme environments. The stress of low temperatures on life is exacerbated in organisms that rely on photoautrophic production of organic carbon and energy sources. Phototrophic organisms must coordinate temperature-independent reactions of light absorption and photochemistry with temperature-dependent processes of electron transport and utilization of energy sources through growth and metabolism. Despite this conundrum, phototrophic microorganisms thrive in all cold ecosystems described and (together with chemoautrophs) provide the base of autotrophic production in low-temperature food webs. Psychrophilic (organisms with a requirement for low growth temperatures) and psychrotolerant (organisms tolerant of low growth temperatures) photoautotrophs rely on low-temperature acclimative and adaptive strategies that have been described for other low-temperature-adapted heterotrophic organisms, such as cold-active proteins and maintenance of membrane fluidity. In addition, photoautrophic organisms possess other strategies to balance the absorption of light and the transduction of light energy to stored chemical energy products (NADPH and ATP) with downstream consumption of photosynthetically derived energy products at low temperatures. Lastly, differential adaptive and acclimative mechanisms exist in phototrophic microorganisms residing in low-temperature environments that are exposed to constant low-light environments versus high-light- and high-UV-exposed phototrophic assemblages.

Acclimatization↗

Local cold acclimation during exercise and its effect on neuromuscular function of the hand.

Most acclimation research is performed on resting individuals, whereas in real life, cold exposure is often accompanied by physical activity. We examined the effects of 2 weeks of repeated cold exposure of the hand with or without an elevated core temperature from exercise on neuromuscular function of the first dorsal interosseus (FDI) muscle and manual performance of the hand. The experimental group (4 female, 6 male; age, 25.1 +/- 6.9 y) cooled their hands in 8 degrees C water for 30 min daily while cycling (50% of heart rate reserve); the control group (4 female, 4 male; age, 25.1 +/- 5.7 y) remained still. Manual function testing consisted of tactile sensitivity, grip strength, manual dexterity, and evoked twitch force in a custom-made myograph. Thermal sensation, skin temperature of index finger (Tif) and hand (Tfdi), as well as rectal temperature (Tre), were recorded daily. Tre increased significantly during bicycling, by 0.6 +/- 0.2 degrees C. Minimal Tif and Tfdi of the groups combined increased significantly during exposure days from 8.7 +/- 0.7 degrees C and 12.4 +/- 2.8 degrees C to 10.1 +/- 1.3 degrees C and 15.0 +/- 3.0 degrees C, respectively (p=0.04), with no significant difference between groups. Thermal ratings improved significantly on exposure days. Manual function was impaired with cooling, but with no significant difference between groups or across time. Deterioration of twitch characteristics with cooling did not change with repeated cold exposure. Although the increasing core temperature during cold water immersion changed the acute temperature response and thermal ratings, it had no effect on local cold acclimation or manual function.

Acclimatization↗

Increased purine nucleotide binding, altered polypeptide composition, and thermogenesis in brown adipose tissue mitochondria of cold-acclimated rats.

Rapid increases in atractyloside-insensitive binding of purine nucleotides (ADP or GDP) and in a polypeptide of 32 000 occur in brown adipose tissue mitochondria of the rat during acclimation to cold. The increased binding is apparent within 1 h and reaches a maximum after 3--7 days of exposure to 4 degrees C. The increase in the 32 000 peptide occurs more slowly and reaches a maximum after 2--3 weeks. There is a simultaneous decrease in a polypeptide of 96 000, apparent after 1 day and reaching a maximum after 1--2 weeks. Results are interpreted in terms of the appearance of an increased amount of the purine nucleotide-sensitive proton conductance pathway in association with the development of an enhanced thermogenic capacity of brown adipose tissue mitochondria during acclimation of the rat to cold.

Acclimatization↗

Altered effect of insulin and catecholamines in brown adipose tissue of cold-acclimated rats.

Data are presented indicating that in brown adipose tissue (BAT) of cold-acclimated (CA), but not cold-exposed (CE) rats, there was an alteration in the relative response to catecholamines and insulin as evidenced by increased binding of alprenolol and decreased binding of insulin to plasma membrane enriched fractions. In addition, the stimulatory effect of insulin on glucose incorporation into glycogen and its inhibitory action on adenylate cyclase activity were both blunted in the CA tissues. It is proposed that shifts in the capacity of BAT to respond to catecholamines and insulin may be involved in the mechanism of cold acclimation.

Acclimatization↗

Stress- and cold-induced adrenocortical responses in repetitively immobilized or cold-acclimated rats.

To evaluate the role of adrenocortical hormones in stress- or cold-induced nonshivering thermogenesis, plasma corticosterone (CS) and deoxycorticosterone (DOCS) were measured with the aid of HPLC under various conditions. Repetitive immobilization stress (3 h/day, for 1 or 4 weeks) elevated the resting level (24 h after the last immobilization) of CS, but not DOCS. Acute stress (immobilization for 30 min) or cold exposure (-5 degrees C for 15 min) caused marked increases of CS and DOCS in both nonstressed naive controls and repetitively stressed rats. Four weeks, but not 1 week, of repetitive immobilization stress potentiated the responsiveness of CS to both acute stress and cold, and that of DOCS to acute stress, but not to cold. Cold acclimation (5 degrees C, 4 weeks) significantly elevated both corticosteroids but did not affect the resting levels (18 h after being transferred to 25 degrees C) or the responsiveness of both CS and DOCS to either acute stress or cold. These results suggest that repetitive immobilization stress, but not cold acclimation, could enhance nonshivering thermogenesis, at least in part, through an improvement in the responsiveness of adrenocortical hormone secretion to acute stress or cold.

Acclimatization↗

PLANT COLD ACCLIMATION: Freezing Tolerance Genes and Regulatory Mechanisms.

Many plants increase in freezing tolerance upon exposure to low nonfreezing temperatures, a phenomenon known as cold acclimation. In this review, recent advances in determining the nature and function of genes with roles in freezing tolerance and the mechanisms involved in low temperature gene regulation and signal transduction are described. One of the important conclusions to emerge from these studies is that cold acclimation includes the expression of certain cold-induced genes that function to stabilize membranes against freeze-induced injury. In addition, a family of Arabidopsis transcription factors, the CBF/DREB1 proteins, have been identified that control the expression of a regulon of cold-induced genes that increase plant freezing tolerance. These results along with many of the others summarized here further our understanding of the basic mechanisms that plants have evolved to survive freezing temperatures. In addition, the findings have potential practical applications as freezing temperatures are a major factor limiting the geographical locations suitable for growing crop and horticultural plants and periodically account for significant losses in plant productivity.

Journal Article↗

Increase in cell size underlies neuron-specific temperature acclimation in Aplysia.

Aplysia californica with similar genetic and environmental backgrounds were raised under mariculture conditions at either 10 or 20 degrees C. Determinations of cell surface area using capacitance and visual measurements indicated that there was an increase in the surface area of identified neurons. However, this increase was cell specific, occurring only in certain identified neurons. The amplitude of the early potassium current (IA) was monitored in identified neurons from the cold- and warm-reared groups during acute changes in temperature. The response to acute temperature change differed in the two groups, indicative of partial temperature acclimation of IA. Cold rearing shifted the acute temperature-response curve for IA amplitude to color temperatures, compared with the temperature-response curve for animals reared at warmer temperatures. This acclimation was related to the increase in surface area previously noted. Cells showing an increase in IA amplitude in cold-reared animals also showed an increase in membrane surface area, presumably associated with an increased number of A-channels, while channel density was unchanged. There was a small but significant shift in the steady-stage voltage dependency of inactivation, whereas kinetic properties were unaffected by rearing temperature.

Acclimatization↗

Structural changes in the apical membrane of lamprey chloride cells after acclimation to seawater.

Freeze-fracture replicas demonstrate that the apical membrane of the chloride cells of young adult lampreys (Geotria australis) undergoes a structural change when the animal is acclimated from freshwater to seawater. Although the particles on both the P face and the E face of this membrane are randomly distributed in freshwater animals, they are usually arranged in clusters on both fracture faces in seawater-acclimated animals. Light optical diffraction analysis demonstrates that the particles forming the clusters are periodically arranged. Although comparable clusters of particles have not been recorded in other epithelial membranes that are engaged in transporting ions into a hypertonic environment, they may be involved in the final step of Cl- secretion by the chloride cells of lampreys in seawater.

Adaptation, Physiological↗

Increased lipogenesis in isolated hepatocytes from cold-acclimated ducklings.

Thermogenic endurance and development of metabolic cold adaptation in birds may critically depend on their ability to synthesize and use fatty acids (FA) as fuel substrates. Hepatic lipogenesis and the capacity to oxidize FA in thermogenic tissues were measured in cold-acclimated (CA) ducklings (Cairina moschata) showing original mechanisms of metabolic cold adaptation in the absence of brown adipose tissue, the specialized thermogenic tissue of rodents. The rate of FA synthesis from [U-(14)C]glucose and from [1-(14)C]acetate, measured in incubated hepatocytes isolated from 5-wk-old thermoneutral (TN; 25 degrees C) or CA (4 degrees C) fed ducklings, was higher than in other species. Hepatic de novo lipogenesis was further increased by cold acclimation with both glucose (+194%) and acetate (+111%) as precursor. Insulin slightly increased (+11-14%) hepatic lipogenesis from both precursors in CA ducklings, whereas glucagon was clearly inhibitory (-29 to -51%). Enhanced de novo lipogenesis was associated with higher (+171%) hepatocyte activity of glucose oxidation and larger capacity (+50 to +100%) of key lipogenic enzymes. The potential for FA oxidation was higher in liver (+61%) and skeletal muscle (+29 to +81%) homogenates from CA than from TN ducklings, suggesting that the higher hepatic lipogenesis may fuel oxidation in thermogenic tissues. Present data underline the high capacity to synthesize lipids from glucose in species like muscovy ducks susceptible to hepatic steatosis. Lipogenic capacity can be further increased in the cold and may represent an important step in the metabolic adaptation to cold of growing ducklings.

Acclimatization↗

IGF-I and branchial IGF receptor expression and localization during salinity acclimation in striped bass.

The initial response of the IGF-I system and the expression and cellular localization of IGF type-I receptor (IGF-IR) were studied in the gill of a euryhaline teleost during salinity acclimation. Exposure of striped bass (Morone saxatilis) to hyperosmotic and hypoosmotic challenges induced small, transitory (<24 h) deflections in hydromineral balance. Transfer from freshwater (FW) to seawater (SW) induced an initial decrease in plasma IGF-I levels after 24 h in both fed and fasted fish. There was an overall decrease in liver IGF-I mRNA levels after SW transfer, suggesting that decreased plasma levels may be due to a decline in hepatic IGF-I synthesis. No changes were observed in gill IGF-I mRNA, but SW transfer induced an increase in gill IGF-IR mRNA after 24 h. Transfer from SW to FW induced an increase in plasma IGF-I levels in fasted fish. In fed fish, no significant changes were observed in either plasma IGF-I, liver, or gill IGF-I mRNA, or gill IGF-IR mRNA levels. In a separate experiment, FW-acclimated fish were injected with saline or IGF-I prior to a 24-h SW challenge. Rapid regain of osmotic balance following SW transfer was hindered by IGF-I. Immunohistochemistry revealed for the first time in teleosts that IGF-IR and Na(+)-K(+)-ATPase are localized in putative chloride cells at the base of the lamellae, identifying these cells in the gill as a target for IGF-I and IGF-II. Overall the data suggest a hyperosmoregulatory role of IGF-I in this species.

Acclimatization↗

Sodium metabolism during acclimation to water restriction by wild mice, Mus musculus.

Changes in sodium and potassium balance and urinary aldosterone excretion (free plus "acid labile") were surveyed in house mice acclimating initially to 1/2 the ad libitum water ration and later to 1/4 of ad libitum. Each water restriction caused negative sodium and potassium balance, followed by conservation of both ions. At the first water restriction, negative balance was produced by natriuresis and kaliuresis, at successive water restriction, a negative balance was due to a decrease in food consumption. Aldosterone excretion doubled at the 1/2 ad libitum restriction, and then generally remained at control levels thereafter. Fractional intestinal absorption of both ions showed a persistent increase after the 3rd day of water restriction. The Na:K ratio in urine and feces declined as mice responded to each water restriction and returned to control levels in acclimated animals.

Acclimatization↗

Metabolic and acid-base changes during selection of warmer water by cold-acclimated fish.

Largemouth bass (Micropterus salmoides) acclimated to 3 degrees C were placed in a thermal gradient. The bass selected the final thermal preferendum of 28 degrees C in about 18 h. The movement into warmer water was initially rapid but became progressively slower. 2) Other bass were acclimated to 8 degrees C, cannulated in the dorsal aorta, and placed in a temperature-controlled chamber. Oxygen uptake, blood pH, and total CO2 were measured as the chamber temperature was increased to 28 degrees C following a time course similar to that followed by bass in the gradient. 3) Oxygen uptake was always elevated above the resting level, and this elevation increased as higher temperatures were encountered. 4) Just prior to placement in the chamber the pH of the arterial blood was 7.98 +/- 0.05 (mean +/- SE). As the temperature was increased neither the pH nor the total CO2 content of the blood exhibited major changes. At temperatures between 26 and 28 degrees C, the pH (8.01 +/- 0.03) was about 0.3 pH units above predicted normal values. 5) During the return to the final thermal preferendum fish experience overall metabolic rates and extracellular acid-base levels that deviate progressively farther from normal resting levels. Neither factor appears likely to be the major determinant of the behavioral response.

Acclimatization↗

Adaptation to extreme ambient temperatures in cold-acclimated gerbils and mice.

To explain tolerance of heat and cold in gerbils (Gerbillus campestris) in their natural environment, a comparative study was made of thermoregulatory reactions in these animals and white mice (Mus musculus) of the same body mass exposed for 2-3 h to ambient temperatures (Ta) ranging from -23 to 40 degrees C. Metabolic rate (MR), evaporative heat loss (EHL), colonic temperature (Tb), and electromyographic activity (EMG) were measured. Nonshivering thermogenesis (NST) was also evaluated from the increase in MR after norepinephrine injection. In gerbils, tolerance of cold was higher than in mice; there was no fall in Tb in cold-acclimated (CA) and control (TN) gerbils after 3 h of exposure at -20 and -10 degrees C Ta, respectively; peak MR (PMR) reached five to six times resting MR (RMR) in gerbils and four to five times in mice. In gerbils, RMR was 35% below that of mice. In TN gerbils, EHL did not increase before 38 degrees C Ta; EHL increased at 26 degrees C in mice. In both animals, cold acclimation increased cold tolerance, PMR, RMR, and NST. Low RMR, high Tb, and mainly burrowing habits preserve gerbils from overheating and save water in hot and arid environments, and a conspicuous tolerance of cold allows them to live and forage in the wild during the cold night.

Acclimatization↗