Membrane Organization of the Desiccation-Tolerant Moss Tortula ruralis in Dehydrated States

Membrane organization of the desiccation tolerant moss Tortula ruralis was studied in several intensely dehydrated states (75% relative humidity [RH], 90% RH, plasmolysis in molar salt, freezing to −20°C) by ³¹P nuclear magnetic resonance and ultrastructural analyses. Both methods revealed that even at 75% RH (−400 bars), the moss cellular membranes retained extended phospholipid bilayers. Ultrastructural analyses of the fully hydrated moss showed an extensive proliferation of membrane vesicles in the endoplasmic reticulum. During dehydration, these vesicles form layers of membrane under the plasmalemma and in some cases appear to fuse with the surface membrane. This suggests that these vesicles may serve as a reservoir of membranes to accommodate for membrane surface area changes during desiccation and subsequent rehydration.     

On the Metabolism of Tortula ruralis Following Desiccation and Freezing: Respiration and Carbohydrate Oxidation

Recovery from desiccation by Tortula ruralis (Hedw.) Gaertn., Meyer and Scherb was accompanied by an immediate, rapid increase in respiration (measured as oxygen uptake) at 25.5°C or 3.5°C. The respiratory burst was greater on rehydration of moss which had been rapidly desiccated over silica gel than that which had been more slowly desiccated in atmospheres of high relative humidity. No respiration was observed in dry moss. Dried moss which had been placed in liquid nitrogen resumed respiration on rewarming and rehydration but moss which had been frozen in the hydrated state respired to a lesser extent and showed signs of freeze damage. In the initial stages of slow drying a slight increase in respiration was noted, followed by a gradual decrease as drought became more severe. In contrast to observations made on many higher plants under drought stress, this moss did not exhibit any changes in its starch and sugar content during or following desiccation, nor were there any changes in free proline levels. Using (1-¹⁴C)-glucose and (6-¹⁴C)-glucose, the relative activities of the Embden–Meyerhof–Parnas and pentose phosphate pathways in hydrated and rehydrated moss were determined, as were the activities of specific enzymes involved in these pathways. An increased activity of the Embden–Meyerhof–Parnas pathway of glucose oxidation on rehydration of Tortula was observed. The possible significance of this latter observation is outlined.     

The Conservation of Polyribosomes in the Moss Tortula ruralis during Total Desiccation

Total desiccation of the moss Tortula ruralis was achieved byplacing it in a dry atmosphere for 90 min. Reintroduction ofthe moss to water resulted in the recovery of its normal morphologicalform within 15–30 s. The sedimentation profile on a sucrosegradient of the ribosomal content of the totally dry moss showsthe presence of distinct polyribosomal peaks. The levels ofthese polyribosomes rise upon rehydration of the moss. The differencebetween the tolerance to water deficit by this moss and by higherplants is outlined.     

Protein Synthesis Related to Cold Temperature Stress in the Desiccation-Tolerant Moss Tortula ruralis

Incubation of hydrated Tortula ruralis (Hedw.) Gaertn., Meyer. Scherb. at temperatures down to 2°C resulted in an accumulation of polyribosomes and a decrease in single ribosomes. No changes in the levels of ribosomal subunits were detected. On rehydration of slowly dried moss, which contains no polyribosomes, these were reormed at 2, 8 and 20°C. Rapid incorporation of labelled leucine into protein was observed on reintroduction of the desiccated plant o water at 20°C and there was significant, but much reduced, ncorporation at 2°C. Previously undesiccated moss was also able o take up radioactive leucine and to synthesize protein at 2 and -2.5°C. Changes in the rate of protein synthesis at low temperature were not detected in cold hardened (winter collected or incubated at 2°C) T. ruralis. The moss appears to be adapted to survive freezing wear round and even summer-collected moss can conduct protein synthesis at low temperatures: seasonal cold hardiness changes do lot appear to take place.     

Plant Desiccation and Protein Synthesis: III. Stability of Cytoplasmic RNA during Dehydration, and Its Synthesis on Rehydration of the Moss Tortula ruralis

RNA species from the haploid gametophyte generation of the moss Tortula ruralis exhibit typical eukaryotic characteristics. The major ribosomal and soluble RNA species are stable during drying and rehydration. RNA synthesis occurs rapidly on reintroduction of the moss to water and incorporation into high molecular weight RNA fractions was detected after 20 to 30 minutes of rehydration and into low molecular weight fractions after 30-60 minutes. Newly synthesized ribosomal RNA was detected in ribosomes within 2 hours of rehydration, but not in polysomes. It is apparent that the ribosomal and transfer RNA conserved during desiccation is involved in the re-establishment of early protein synthesis during subsequent rehydration and that, initially, there is no requirement for newly synthesized material.     

Drought Stress, Enzymes of Glutathione Metabolism, Oxidation Injury, and Protein Synthesis in Tortula ruralis

The activities of glutathione reductase (EC 1.6.4.2), glutathione peroxidase (EC 1.11.1.9), and glutathione S-transferase (EC 2.5.1.18) were found to increase during slow drying or during rehydration following rapid drying of the drought-tolerant moss Tortula ruralis. Little change was observed in the activity of malate deydrogenase (NAD⁺ oxidoreductase, EC 1.1.1.37) during dehydration or subsequent rehydration. When the tissue was treated with cycloheximide, actinomycin D, or cordycepin, the increase in the activities of glutathione reductase and glutathione S-transferase was largely prevented while effect on glutathione peroxidase was much smaller. Concomitantly, oxidized glutathione (GSSG) as percentage of total glutathione increased. GSSG level was correlated positively with the levels of lipid peroxidation and solute leakage and negatively with the rate of protein synthesis. The results show that GSSG level is a good indicator of oxidation stress and provide support to the suggestion that GSSG mediates, at least in part, the drought stress-induced inhibition of protein synthesis.     

Plant Desiccation and Protein Synthesis : VI. Changes in Protein Synthesis Elicited by Desiccation of the Moss Tortula ruralis are Effected at the Translational Level

Upon rehydration of the moss Tortula ruralis following desiccation at a rapid or slow rate, there is increasing utilization of newly synthesized-poly(A)⁺ RNA for protein synthesis. Initially, poly(A)⁺ RNA conserved in the dry moss is associated with polysomes, but by 2 hours of rehydration there is an overwhelming recruitment of newly synthesized poly(A)⁺ RNA, at the expense of conserved messages. In rehydrated moss, there is a marked synthesis in vivo of new proteins, which are separable by two-dimensional electrophoresis, and identifiable by fluorography. These new proteins, termed rehydration proteins, are synthesized after both rapid and slow desiccation, but their synthesis persists longer after rapid desiccation. The protein patterns obtained following in vitro translation of bulk RNA from hydrated, desiccated, and rehydrated moss were qualitatively identical. Thus the differences in protein patterns observed in vivo must result from preferential selection of specific mRNAs from the same pool, which is indicative of control of protein synthesis at the translational level. The implications of these observations in relation to the response of the moss to drying in its natural environment are discussed.     

Plant Desiccation and Protein Synthesis. IV. RNA Synthesis, Stability, and Recruitment of RNA into Protein Synthesis during Desiccation and Rehydration of the Desiccation-Tolerant Moss, Tortula ruralis

We have studied the effects of ATP and ADP on the oxidation of malate by coupled and uncoupled mitochondria prepared from etiolated hypocotyls of mung bean (Vigna radiata L.).

In coupled mitochondria, ATP (1 millimolar) increased pyruvate production and decreased oxaloacetate formation without altering the rate of oxygen consumption. ATP also significantly decreased oxaloacetate production and increased pyruvate production in mitochondria that were uncoupled by carbonyl cyanide p-trifluoromethoxyphenyl hydrazone plus oligomycin.

In coupled mitochondria, ADP (1 millimolar) increased the production of both pyruvate and oxaloacetate concomitantly with the acceleration of oxygen uptake to the state 3 rate. The effects of ADP were largely eliminated in uncoupled mitochondria. These results indicate that, whereas the ADP stimulation of oxaloacetate and pyruvate production in the coupled mitochondria is brought about primarily as the result of the accelerated rates of electron transport and NADH oxidation by the respiratory chain in state 3, ATP has significant regulatory effects independent of those that might be exerted by control of electron transport.

     

Influence of Protoplasmic Water Loss on the Control of Protein Synthesis in the Desiccation-Tolerant Moss Tortula ruralis: Ramifications for a Repair-Based Mechanism of Desiccation Tolerance

Desiccation tolerance of the moss Tortula ruralis is characterized by a desiccation-induced change in gene expression that becomes evident upon rehydration. As reported earlier, this change in gene expression is apparently brought about by a change in the control of translation and does not include a major shift in mRNA abundance. A full qualitative and quantitative analysis of the alteration in gene expression, which is characterized by the loss of (or greater than fivefold decrease in) the synthesis of 25 hydration (h) proteins and initiation (or greater than fivefold increase) of the synthesis of 74 rehydration (r) proteins, is given in this report. Exposure to a desiccating atmosphere, for times that result in varying levels of water loss, enabled the determination that the control of synthesis of r proteins is different from the control of synthesis of h proteins. The r and h protein synthesis responses are internally coordinate, however. Similarly, the return to normal levels of h protein synthesis differs from that of the r proteins. The return to normal synthetic levels for all h proteins is synchronous, but the rate of loss of r protein synthesis varies with each individual r protein. Run-off translation of polysomes isolated from gametophytes during the drying phase demonstrates that there are no novel mRNAs recruited and no particular mRNA is favored for translation during desiccation. These findings add credence to the argument that translational control is the major component of the desiccation-induced alteration in gene expression in this plant, as discussed. Aspects of the response of protein synthesis to desiccation are consistent with the hypothesis that T. ruralis exhibits a repair-based mechanism of desiccation tolerance.     

Diurnal variation in photochemical dynamics and surface reflectance of the desiccation-tolerant moss,Tortula ruralis

Most desiccation-tolerant plants alter shoot structure during drying, making it possible to use changes in surface reflectance as a proxy measure of plant water status. Diurnal courses of surface reflectance (albedo) and chlorophyll fluorescence parameters of the ectohydric moss, Tortula ruralis (Hedw.) Gaertn, were measured to assess the coordination between anatomical and physiological features under field conditions. Albedo showed a sigmoidal relationship with relative humidity and the deviation of moss mat temperature from dew point. Maximum photosynthetic quantum yield (F _v/F _m) also displayed a sigmoidal relationship pooled across three days differing in light, temperature, and relative humidity. Depending on the light conditions and rapidity of drying during the morning, there were distinct differences in the ability of T. ruralis to establish thermal dissipation of excess light energy (NPQ) across a range of light levels following rehydration through the day. These findings suggest that there is a coordinated suite of architectural and physiological characteristics maintaining the photosynthetic integrity of these plants in highly variable arid and semi-arid environments.     

Plant Desiccation and Protein Synthesis : V. Stability of Poly (A) and Poly (A) RNA during Desiccation and Their Synthesis upon Rehydration in the Desiccation-Tolerant Moss Tortula ruralis and the Intolerant Moss Cratoneuron filicinum

Upon desiccation of gametophytes of the desiccation-tolerant moss Tortula ruralis preexisting pools of poly(A)⁻ RNA (rRNA) remain inact, regardless of the speed at which desiccation is achieved. Preexisting poly(A)⁺ RNA pools (mRNA) are unaffected by slow desiccation but are substantially reduced during rapid desiccation. Poly(A)⁻ RNA involved in protein synthesis is also unaffected by desiccation, whereas the levels of polysomal poly(A)⁺ RNA in rapid- and slow-dried moss closely reflect the state of the protein synthetic complex in these dried samples.

Poly(A)⁻ RNA pools, both total and polysomal, are also stable during the rehydration of both rapid- and slow-dried moss. The total poly(A)⁺ RNA pool decreases upon rehydration, but this reduction is simply an expression of the normal turnover of poly(A)⁺ RNA in this moss. Analysis of polysomal fractions during rehydration reveals the continued use of conserved poly(A)⁺ RNA for protein synthesis. The rate of synthesis of poly(A)⁺ RNA upon rehydration appears to depend upon the speed at which prior desiccation is administered. Rapidly dried moss synthesizes poly(A)⁺ RNA at a faster rate, 60 to 120 minutes after the addition of water, than does rehydrated slowly dried moss. Recruitment of this RNA into the protein synthetic complex also follows this pattern. Comparative studies involving the aquatic moss Cratoneuron filicinum are used to gain an insight into the relevance of these findings with respect to the cellular mechanisms associated with desiccation tolerance.

     

Exaggeration of desiccation stress by heavy metal pollution in Tortula ruralis: a pilot study

Glutathione pool and redox status, as well as chlorophyll fluorescencewere measured in Tortula ruralis which was treated withheavy metals and exposed to different desiccation treatments. Two hours afterre-wetting, the ratio of oxidised glutathione to total glutathione poolreturnedto the steady state level (14%) in slowly dried unpolluted plants. Cdtreatment doubled this ratio, as did rapid drying without the heavy metaltreatment. When Cd and rapid drying were applied together, the ratio of GSSGreached 45% indicating a clear additive effect of these two stressfactors. RFd, a chlorophyll fluorescence parameter followed a similar pattern.Lead did not cause the depletion of the glutathione pool but increased theratioof GSSG. It is suggested that Cd and rapid desiccation exert their damageadditively. This might also entail a lowered degree of desiccation tolerance inareas polluted with metals and therefore a retreat of the mosses to mesicmicrohabitats.     

Early morning photosynthesis of the moss Tortula ruralis following summer dew fall in a Hungarian temperate dry sandy grassland

Air temperature and humidity, moss surface temperature, moss water content, and photosynthetically active radiation were measured through a clear dry night and early morning in July 1998; CO₂ gas exchange of the moss was measured by infra-red gas analysis. The measurements showed progressive absorption of water by the moss through much of the night. The moss reached sufficient water content for about 1.5 h of positive net CO₂ uptake immediately after dawn. The cumulative net carbon balance on this occasion was negative, but mornings with heavier dew could give a positive daily carbon balance, and short, early morning periods of photosynthesis during prolonged dry weather may mitigate long-term desiccation damage and allow for regular molecular repair.     

Bryophytes as experimental models for the study of environmental stress tolerance: Tortula ruralis and desiccation-tolerance in mosses

The development of a complete understanding of how plants interact with the environment at the cellular level is a crucial step in advancing our ability to unravel the complexities of plant ecology particularly with regard to the role that many of the less complex plants (i.e., algae, lichens, and bryophytes) play in plant communities and in establishing areas for colonization by their more complex brothers. One of the main barriers to the advancement of this area of plant biology has been the paucity of simple and appropriate experimental models that would enable the researcher to biochemically and genetically dissect the response of less complex plants to environmental stress. A number of bryophytes model systems have been developed and they have been powerful experimental tools for the elucidation of complex biological processes in plants. Recently there has been a resurgent interest in bryophytes as models systems due to the discovery and development of homologous recombination technologies in the moss Physcomitrella patens (Hedw.) Brach & Schimp. In this report we introduce the desiccation-tolerant moss Tortula ruralis (Hedw.) Gaert., Meyer, and Scherb, as a model for stress tolerance mechanisms that offers a great deal of promise for advancing our efforts to understand how plants respond to and survive the severest of stressful environments. T. ruralis, a species native to Northern and Western North America, has been the most intensely studied of all bryophytes with respect to its physiological, biochemical, and cellular responses, to the severest of water stresses, desiccation. It is our hope that the research conducted using this bryophyte will lay the foundationfor not only the ecology of bryophytes and other less complex plants but also for the role of desiccation-tolerance in the evolution of land plants and the determination of mechanisms by which plant cells can withstand environmental insults. We will focus the discussion on the research we and others have conducted in an effort to understand the ability of T. ruralis to withstand the complete loss of free water from the protoplasm of its cells.     

Expressed sequence tags (ESTs) from desiccated Tortula ruralis identify a large number of novel plant genes.

The desiccation-tolerant moss Tortula ruralis [Hedw.] Gaerten., Meyer & Scherb. has both a constitutive protection system and an active rehydration induced recovery mechanism apparently unique to bryophytes. Immediately following rehydration, desiccated T.ruralis gametophytes produce a set of polypeptides whose synthesis is unique to the rehydrated state. We report the construction of a cDNA expression library from the polysomal mRNA of desiccated gametophytes and the single-pass sequencing of randomly selected clones. 152 expressed sequence tags (ESTs) were generated representing more than 60,000 bp of non-redundant DNA sequence. 44 ESTs (29%) demonstrated significant homology to previously identified nucleotide and/or polypeptide sequences, such as ribosomal proteins, desiccation-related peptides, early light-inducible proteins and a V-type ATPase. Analysis of a subset of these homologous ESTs reveals that codon preference in T.ruralis is similar to that of vascular plants, particularly the Magnoliopsida. 108 ESTs (71%) demonstrated no significant homology to deposited sequences and represent a large number of novel plant genes. Analysis of these ESTs will define the range of genes involved in cellular repair and recovery and may provide greater insight to the complex phenotype of vegetative desiccation-tolerance.     

Water Stress and Protein Synthesis: V. Protein Synthesis, Protein Stability, and Membrane Permeability in a Drought-sensitive and a Drought-tolerant Moss

The effects have been studied of water stress and desiccation on protein synthesis in the drought-tolerant moss Tortula ruralis and the drought-sensitive moss Hygrohypnum luridum. At any particular level of steady state water stress, the inhibition of protein synthesis was greater in H. luridum than in T. ruralis. Water stress-induced changes in the pattern of protein synthesis, as determined by the double label ratio technique, were minor in T. ruralis, but major in H. luridum. Proteins of both mosses were found to be stable during desiccation and subsequent rehydration. Changes in membrane permeability, as indicated by the leakage of amino acid, were observed during rehydration of desiccated moss and were dependent on the rate of desiccation. The leakage was small and reversible in T. ruralis but large and irreversible in H. luridum. Although H. luridum failed to recover from complete desiccation (80% loss in fresh weight), it was able to recover fully from steady state stress under conditions where a maximum loss of 55% in fresh weight was recorded.     

冻结速率对血小板冷冻干燥保存的影响

冷冻干燥法是使血小板能够长期保存的一种理想方法。冻结过程对血小板的冻干保存至关重要。采用梯度降温、搁板预冷、液氮冻结等三种冻结方式,研究了冻结速率对血小板冷冻干燥保存恢复率的影响。实验结果表明用搁板预冷的方式冻结并干燥的血小板复水后的恢复率最高,达到(93.0.2)%,此时的冻结速度约为10℃/min。扫描电镜照片显示冻干复水后的血小板保持了完整的细胞结构,但与新鲜血小板相比略呈球形。冻干复水后的血小板对1U/ml凝血酶的最大聚集率接近于新鲜血小板,但聚集速度比新鲜血小板慢。