Cellular and tissue distribution of potassium: Physiological relevance,mechanisms and regulation

Potassium (K⁺) is the most important cationic nutrient for all living organisms. Its cellular levels are significant (typically around 100 mM) and are highly regulated. In plants K⁺ affects multiple aspects such as growth, tolerance to biotic and abiotic stress and movement of plant organs. These processes occur at the cell, organ and whole plant level and not surprisingly, plants have evolved sophisticated mechanisms for the uptake, efflux and distribution of K⁺ both within cells and between organs.     

Potassium Substitution by Sodium in Plants

Soil salinity is an ever-increasing constraint to crop productivity worldwide especially in countries with irrigated agriculture. In contrast to all the soil reclamation strategies to decrease salt concentrations in root zone, the use of sodium (Na⁺) in plant nutrition may be an interesting tactic. The roles of potassium (K⁺) and Na⁺ in plant nutrition suggest that K⁺ is the only monovalent cation which is essential for most higher plants and is involved in three important functions, i.e., enzyme activation, charge balance and osmoregulation. Plants need a small amount but high concentration of K⁺ for specific functions in the cytoplasm and a major portion (～90%) of it is localized in vacuoles, where it acts as an osmoticum. Maintenance of osmotic potential in vacuoles, a nonspecific function of K⁺, can be achieved by other cations such as Na⁺. For decades an ample amount of work has been done on the substitution of K⁺ by Na⁺ in plant nutrition. In this regard, Na⁺ has the potential to replace K⁺ for some of its functions. In some plants, supplementation of Na⁺ in reduced amounts can eliminate K⁺ deficiency symptoms under limited K⁺ supply. Thus, the question of K⁺ substitution by Na⁺ in plant physiology is not only of academic interest but has considerable practical implications in relation to fertilizer management and plant growth in salt-affected environments. In this review, we discuss the possibilities of K⁺ substitution by Na⁺ under specific soil and environmental conditions.     

The role of plant cation/proton antiporter gene family in salt tolerance

Salinity is one of the major abiotic constraints to agriculture. The physiological and molecular mechanisms of salt tolerance have been studied in plants for many years. The regulation of osmosis and ion homeostasis is crucial. A lot of important components involved in plant responses to salt stress have been identified. Among them, ion transporters and channels take an essential role in ion homeostasis, mainly for Na⁺, Cl^-, and K⁺. Until now, many cation antiporters important for salt tolerance in plants have been characterized. Among them, the monovalent cation/proton antiporters (CPA) family is one of the most important families, including sodium proton exchangers (NHXs), K⁺-efflux antiporters (KEAs), and cation/H⁺ exchangers (CHXs). Here, the current knowledge of the plant CPA family in responses to salt stress is reviewed. The regulation mechanisms were also included and discussed.     

Potassium: a vital nutrient mediating stress tolerance in plants

Nutrients have been known to affect stress conditions, in fact, nutrient deprivations are stress conditions for plants itself. Likewise, three important nutrients Nitrogen (N), Phosphorus (P) and Potassium (K) mediates major stress responses in plants. Here, involvement of K has been discussed briefly in plant stress response along with its impact on plant development. K has been regarded as immensely important nutrient in agriculture, hence, its deficiency triggers various signaling cascades, finally enabling plants to activate stress adaptation responses. So far, K⁺ has been reported to play pivotal role in various abiotic stresses such as drought, cold, water stresses etc. However, the exact mechanism and interplay of these different abiotic stress regulation by K⁺ is not completely explored and demand further functional investigations. The in-depth understanding of components involved in K⁺ sensing, transport, and homeostasis will enable plant biologist to engineer crop varieties tolerant to abiotic stresses and nutrient deficient soil in near future.

     

Expression of animal CED-9 anti-apoptotic gene in tobacco modifies plasma membrane ion fluxes in response to salinity and oxidative stress

Apoptosis, one form of programmed cell death (PCD), plays an important role in mediating plant adaptive responses to the environment. Recent studies suggest that expression of animal anti-apoptotic genes in transgenic plants may significantly improve a plant’s ability to tolerate a variety of biotic and abiotic stresses. The underlying cellular mechanisms of this process remain unexplored. In this study, we investigated specific ion flux “signatures” in Nicotiana benthamiana plants transiently expressing CED-9 anti-apoptotic gene and undergoing salt- and oxidative stresses. Using a range of electrophysiological techniques, we show that expression of CED-9 increased plant salt and oxidative stress tolerance by altering K⁺ and H⁺ flux patterns across the plasma membrane. Our data shows that PVX/CED-9 plants are capable of preventing stress-induced K⁺ efflux from mesophyll cells, so maintaining intracellular K⁺ homeostasis. We attribute these effects to the ability of CED-9 to control at least two types of K⁺-permeable channels; outward-rectifying depolarization-activating K⁺ channels (KOR) and non-selective cation channels (NSCC). A possible scenario linking CED-9 expression and ionic relations in plant cell is suggested. To the best of our knowledge, this study is the first to link “ion flux signatures” and mechanisms involved in regulation of PCD in plants.     

Response of Strawberry Plant cv. ‘Camarosa’ to Salicylic Acid and Methyl Jasmonate Application Under Salt Stress Condition

The possible role of salicylic acid (SA) and methyl jasmonate (MJ) treatments on the physiology responses and growth of strawberry (Fragaria?×?ananassa) cv. ‘Camarosa’ subjected to the different levels of salinity stress were investigated. Root and shoot growth as well as their Na⁺/K⁺ ratio, photosynthetic-related factors, and activity of some important antioxidant enzymes were determined in the salt-treated plants. Results indicated that salt stress reduced plant performance especially at higher concentrations. By increasing the levels of salinity stress, fresh and dry weight of shoot and roots, net photosynthetic rate (Pn), and stomatal conductance (Gs) significantly decreased, whereas intercellular CO₂ (Ci) increased. Application of exogenous SA and MJ significantly improved the plant physiological characters as well as fresh and dry weight of shoots and roots. Moreover, the ratio of Na⁺/K⁺ was elevated in the leaves and roots concomitantly with salinity levels, whereas SA and MJ treatments significantly reduced this ratio. Results of enzymatic assays showed that activity of ascorbate peroxidase, peroxidase, and superoxide dismutase enzymes increased in the salt-stressed plants. In addition, SA and MJ treatments reduced the destructive effects of salinity in strawberry plant. In general, among the tested concentrations, 0.5 mM SA and 0.25 mM MJ best increased the activity of antioxidant enzymes and hence alleviated the detrimental effects of salinity stress.     

Sodium and potassium relations of Spergularia marina following N and P deprivation: results of short-term growth studies

In this, we consider the coordination of plant growth and ion acquisition, reporting the short-term adjustments of growth and K⁺ and Na⁺ relations which follow when plants are subject to a sudden deprivation of N and P. The plant used for the experiments, Spergularia marina (L.) Grieseb., is a small coastal halophyte, and the growth medium was 0.2 × modified seawater. By considering nutrients whose availability has not been changed, we report on an aspect of organismal integration which has received little attention either experimentally or in mathematical models. The studies are limited to the first 60 h after N and P deprivation in order to consider changes that, if they are not primary responses, are not temporally remote, passive adjustments. For growth analyses, plants were used approximately 30 days after germination and 16 days after transfer to solution culture. Random harvests were made at hourly invervals, and after 12 h, one-half of the plants were transferred to cultures without N or P. Tissue analyses were used to calculate relative growth rates, relative accumulation rates and net uptake rates. For comparison, isotope uptake studies using ⁴²K⁺ and ²²Na⁺ were conducted at 12, 36 and 60 h after deprivation. The effects on growth and biomass allocation were very rapid, detectable within 13 h. K⁺ transport also responded quickly, and from the beginning of the study, there was essentially no net translocation of K⁺ to the shoot. Isotope studies confirmed the responsiveness, with translocation reduced 33 and 90% after 12 and 36 h, respectively. Though Na⁺ adjustments were slower, they were coordinated with growth such that tissue concentrations in the N and P-deprived plants were comparable to those in the controls. We conclude that N and C are insufficient elements on which to build mathematical models useful to environmental physiologists. At a minimum, the incorporation of K⁺ relations in growth models would both allow the development of the osmotic potential needed to drive cell expansion, and provide a means to probe –experimentally as well as mathematically – the coordinating mechanisms of plant growth and resource management.     

Conditions controlling relative uptake of potassium and rubidium by plants from soils

Earlier studies have demonstrated close inverse relationships between Rb⁺ concentrations in plants and pH or base (including K⁺) saturation of soils. This study aims at elucidating conditions in soils influencing plant uptake of Rb⁺. Growth experiments with Carex pilulifera L. were performed, modifying the acidity and K⁺ supply of acid soils and solutions. We were unable to assess any reduction in Rb⁺ uptake by adding precipitated CaCO₃ to acid soil unless pH was raised to near neutrality. Though not fully compensating the loss of soil solution K⁺and exchangeable K⁺ from uptake by the growing plants, soil treated with 0.5 mM K⁺ (as KCl) reduced the Rb⁺ concentration in the shoots by 40% without measurably changing soil pH. Experiments varying the pH and K⁺ concentration of a nutrient solution (20% Hoagland), spiked with 6 uM Rb⁺, clearly demonstrated that plant uptake of Rb⁺ and K⁺ was unaffected by acidity in the pH range 3.6–5.0 tested, whereas Rb⁺ uptake was reduced by ca. 50%, when K⁺ concentration was increased from 1.2 to 3.6 mM. The sensitivity of this reaction indicates that shortage or low availability of K⁺ controls Rb⁺ uptake from acid soils, being probably more important than soil acidity per se. Secondary effects of high soil acidity, such as leaching losses of K⁺, might also be of importance in accounting for the high uptake of Rb⁺ from such soils. It is suggested that leaf analysis of Rb⁺ may be used as a method to assess early stages of K⁺ deficiency in plants on acid soils.     

Milkweed butterfly resistance to plant toxins is linked to sequestration,not coping with a toxic diet

Insect resistance to plant toxins is widely assumed to have evolved in response to using defended plants as a dietary resource. We tested this hypothesis in the milkweed butterflies (Danaini) which have progressively evolved higher levels of resistance to cardenolide toxins based on amino acid substitutions of their cellular sodium–potassium pump (Na⁺/K⁺-ATPase). Using chemical, physiological and caterpillar growth assays on diverse milkweeds (Asclepias spp.) and isolated cardenolides, we show that resistant Na⁺/K⁺-ATPases are not necessary to cope with dietary cardenolides. By contrast, sequestration of cardenolides in the body (as a defence against predators) is associated with the three levels of Na⁺/K⁺-ATPase resistance. To estimate the potential physiological burden of cardenolide sequestration without Na⁺/K⁺-ATPase adaptations, we applied haemolymph of sequestering species on isolated Na⁺/K⁺-ATPase of sequestering and non-sequestering species. Haemolymph cardenolides dramatically impair non-adapted Na⁺/K⁺-ATPase, but had systematically reduced effects on Na⁺/K⁺-ATPase of sequestering species. Our data indicate that major adaptations to plant toxins may be evolutionarily linked to sequestration, and may not necessarily be a means to eat toxic plants. Na⁺/K⁺-ATPase adaptations thus were a potential mechanism through which predators spurred the coevolutionary arms race between plants and insects.     

Transport,signaling, and homeostasis of potassium and sodium in plants

Potassium （K＋） is an essential macronutrient in plants and a lack of K＋ significantly reduces the potential for plant growth and development. By contrast, sodium （Na＋）, while beneficial to some extent, at high concentrations it disturbs and inhibits various physiological processes and plant growth. Due to their chemical similarities, some functions of K＋ can be undertaken by Na＋ but K＋ homeostasis is severely affected by salt stress, on the other hand. Recent advances have highlighted the fascinating regulatory mechanisms of K＋ and Na＋ transport and signaling in plants. This review summarizes three major topics： （i） the transport mechanisms of K＋ and Na＋ from the soil to the shoot and to the cellular - compartments; （ii） the mechanisms through which plants sense and respond to K＋ and Na＋ availability; and （iii） the components involved in maintenance of K＋/Na＋ homeostasis in plants under salt stress.     

Amino acids regulate salinity-induced potassium efflux in barley root epidermis

The amino acid content increases substantially in salt-stressed plants. The physiological relevance of this phenomenon remains largely unknown. Using the MIFE ion flux measuring technique, we studied the effects of physiologically relevant concentrations of 26 amino acids on NaCl-induced K⁺ flux from barley root epidermis. We show that 21 (of 26) amino acids caused a significant mitigation of the NaCl-induced K⁺ efflux, while valine and ornithine substantially enhanced the detrimental effects of salinity on K⁺ homeostasis. Our results suggest that physiologically relevant concentrations of free amino acids might contribute to plant adaptive responses to salinity by regulating K⁺ transport across the plasma membrane, thus enabling maintenance of an optimal K⁺/Na⁺ ratio as opposed to being merely a symptom of plant damage by stress. Investigating the specific mechanisms of such amelioration remains a key issue for future studies.     

A laser ablation technique maps differences in elemental composition in roots of two barley cultivars subjected to salinity stress

In saline soils, high levels of sodium (Na⁺) and chloride (Cl^?) ions reduce root growth by inhibiting cell division and elongation, thereby impacting on crop yield. Soil salinity can lead to Na⁺ toxicity of plant cells, influencing the uptake and retention of other important ions [i.e. potassium (K⁺)] required for growth. However, measuring and quantifying soluble ions in their native, cellular environment is inherently difficult. Technologies that allow in situ profiling of plant tissues are fundamental for our understanding of abiotic stress responses and the development of tolerant crops. Here, we employ laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) to quantify Na, K and other elements [calcium (Ca), magnesium (Mg), sulphur (S), phosphorus (P), iron (Fe)] at high spatial resolution in the root growth zone of two genotypes of barley (Hordeum vulgare) that differ in salt‐tolerance, cv. Clipper (tolerant) and Sahara (sensitive). The data show that Na⁺ was excluded from the meristem and cell division zone, indicating that Na⁺ toxicity is not directly reducing cell division in the salt‐sensitive genotype, Sahara. Interestingly, in both genotypes, K⁺ was strongly correlated with Na⁺ concentration, in response to salt stress. In addition, we also show important genetic differences and salt‐specific changes in elemental composition in the root growth zone. These results show that LA‐ICP‐MS can be used for fine mapping of soluble ions (i.e. Na⁺ and K⁺) in plant tissues, providing insight into the link between Na⁺ toxicity and root growth responses to salt stress.     

The bare necessities of plant K+ channel regulation

Potassium (K⁺) channels serve a wide range of functions in plants from mineral nutrition and osmotic balance to turgor generation for cell expansion and guard cell aperture control. Plant K⁺ channels are members of the superfamily of voltage-dependent K⁺ channels, or Kv channels, that include the Shaker channels first identified in fruit flies (Drosophila melanogaster). Kv channels have been studied in depth over the past half century and are the best-known of the voltage-dependent channels in plants. Like the Kv channels of animals, the plant Kv channels are regulated over timescales of milliseconds by conformational mechanisms that are commonly referred to as gating. Many aspects of gating are now well established, but these channels still hold some secrets, especially when it comes to the control of gating. How this control is achieved is especially important, as it holds substantial prospects for solutions to plant breeding with improved growth and water use efficiencies. Resolution of the structure for the KAT1 K⁺ channel, the first channel from plants to be crystallized, shows that many previous assumptions about how the channels function need now to be revisited. Here, I strip the plant Kv channels bare to understand how they work, how they are gated by voltage and, in some cases, by K⁺ itself, and how the gating of these channels can be regulated by the binding with other protein partners. Each of these features of plant Kv channels has important implications for plant physiology.     

Root high-affinity K+ and Cs+ uptake and plant fertility in tomato plants are dependent on the activity of the high-affinity K+ transporter SlHAK5

Root K⁺ acquisition is a key process for plant growth and development, extensively studied in the model plant Arabidopsis thaliana. Because important differences may exist among species, translational research supported by specific studies is needed in crops such as tomato. Here we present a reverse genetics study to demonstrate the role of the SlHAK5 K⁺ transporter in tomato K⁺ nutrition, Cs⁺ accumulation and its fertility. slhak5 KO lines, generated by CRISPR-Cas edition, were characterized in growth experiments, Rb⁺ and Cs⁺ uptake tests and root cells K⁺-induced plasma membrane depolarizations. Pollen viability and its K⁺ accumulation capacity were estimated by using the K⁺-sensitive dye Ion Potassium Green 4. SlHAK5 is the major system for high-affinity root K⁺ uptake required for plant growth at low K⁺, even in the presence of salinity. It also constitutes a pathway for Cs⁺ entry in tomato plants with a strong impact on fruit Cs⁺ accumulation. SlHAK5 also contributes to pollen K⁺ uptake and viability and its absence produces almost seedless fruits. Knowledge gained into SlHAK5 can serve as a model for other crops with fleshy fruits and it can help to generate tools to develop low Cs⁺ or seedless fruits crops.     

Overexpression of a novel soybean gene modulating Na+ and K+ transport enhances salt tolerance in transgenic tobacco plants

Salt is an important factor affecting the growth and development of soybean in saline soil. In this study, a novel soybean gene encoding a transporter (GmHKT1) was identified and its function analyzed using transgenic plants. GmHKT1 encoded a protein of 419 amino acids, with a potential molecular mass of 47.06 kDa and a predicted pI value of 8.59. Comparison of the genomic and cDNA sequences of GmHKT1 identified no intron. The deduced amino acid sequence of GmHKT1 showed 38–49% identity with other plant HKT‐like sequences. RT‐PCR analysis showed that the expression of GmHKT1 was upregulated by salt stress (150 mM NaCl) in roots and leaves but not in stems. Overexpression of GmHKT1 significantly enhanced the tolerance of transgenic tobacco plants to salt stress, compared with non‐transgenic plants. To investigate the role of GmHKT1 in K⁺ and Na⁺ transport, we compared K⁺ and Na⁺ accumulation in roots and shoots of wild‐type and transgenic tobacco plants. The results suggested that GmHKT1 is a transporter that affected K⁺ and Na⁺ transport in roots and shoots, and regulated Na⁺/K⁺ homeostasis in these organs. Our findings suggest that GmHKT1 plays an important role in response to salt stress and would be useful in engineering crop plants for enhanced tolerance to salt stress.     

Properties of Shaker-type Potassium Channels in Higher Plants

Potassium (K⁺), the most abundant cation in biological organisms, plays a crucial role in the survival and development of plant cells, modulation of basic mechanisms such as enzyme activity, electrical membrane potentials, plant turgor and cellular homeostasis. Due to the absence of a Na⁺/K⁺ exchanger, which widely exists in animal cells, K⁺ channels and some type of K⁺ transporters function as K⁺ uptake systems in plants. Plant voltage-dependent K⁺ channels, which display striking topological and functional similarities with the voltage-dependent six-transmembrane segment animal Shaker-type K⁺ channels, have been found to play an important role in the plasma membrane of a variety of tissues and organs in higher plants. Outward-rectifying, inward-rectifying and weakly-rectifying K⁺ channels have been identified and play a crucial role in K⁺ homeostasis in plant cells. To adapt to the environmental conditions, plants must take advantage of the large variety of Shaker-type K⁺ channels naturally present in the plant kingdom. This review summarizes the extensive data on the structure, function, membrane topogenesis, heteromerization, expression, localization, physiological roles and modulation of Shaker-type K⁺ channels from various plant species. The accumulated results also help in understanding the similarities and differences in the properties of Shaker-type K⁺ channels in plants in comparison to those of Shaker channels in animals and bacteria.     

Long-term effects of plant hormones on K+ levels and transport in young wheat plants of different K+ status

Long-term effects of 1-naphtaleneacetic acid (NAA), benzyladenine (BA), gibberellic acid (GA₃), abscisic acid (ABA) and ethylene on K⁺ levels, K⁺ uptake and translocation to the shoot were studied in young wheat plants (Triticum aesticum L. cv. Martonvásári-8) grown at different K⁺ supplies. Na⁺ levels and K⁺/Na⁺ selectivity were also investigated. Both in shoots and roots, NAA, BA and ABA decreased K⁺ and Na⁺ levels more effectively in high-K⁺ plants than in low-K⁺ plants. GA, and ethylene did not influence K⁺ and Na⁺ levels. K⁺/Na⁺ selectivity in roots of low-K⁺ plants was increased in favour of K⁺ by BA, NAA and to a lesser extent by ABA. In high-K⁺ plants only BA increased the K⁺/Na⁺ ratio, whereas the effects of the other hormones were the opposite (NAA) or less pronounced (ABA). K⁺(⁸⁶Rb) uptake was inhibited by NAA and BA in low-K⁺ plants but not in high-K⁺ plants. K⁺(⁸⁶Rb) uptake was inhibited throughout by 10 μM ABA. K⁺(⁸⁶Rb) translocation to the shoot was influenced by the hormones similarly to the uptake patterns, with the exception of ABA, which inhibited translocation in low-K⁺ plants but not in high-K⁺ plants. The results show that hormonal effects may quantitatively and qualitatively be modified by K⁺ levels in the plant and that internal K⁺ concentration may play a role in the mechanisms regulating the effects of NAA, BA and ABA but probably not in those of GA₃ or ethylene.     

Ability of symbiotic and non-symbiotic rhizospheric microflora of maize (Zea mays) to weather micas and to promote plant growth and plant nutrition

Summary Maize was grown under axenic conditions in laboratory devices, in a K⁺-deficient medium, where biotite was the K⁺ source. In different treatments plants were inoculated by symbiotic (Glomus mosseae) and/or non symbiotic microflora. In those treatments inoculated byGlomus mosseae, the percentage of roots infection after 7 weeks plant growth was 65%. Rhizospheric bacterial population was approximately 10⁸/g (dry weight). Endomycorrhizae stimulated growth and K uptake. Non-symbiotic microflora increased also plant growth but promoted much more biotite weathering and K uptake. Endomycorrhizae and more particularly non-symbiotic microflora increased also Ca and Mg absorption by plants. Possible mechanisms involved and implications in plant growth and pedogenesis are discussed.