The leaves of trees emit significant amounts of acetaldehyde tion of CAT by aminotriazole did not affect acetaldehyde and which is synthesized there by the oxidation of ethanol. In the ethanol emission, it is concluded that the oxidation of ethanol present study, we examined plant internal and environmental in the leaves is mediated by ADH rather than by CAT. factors controlling the emission of acetaldehyde by the leaves Further studies indicated that aldehyde dehydrogenase of young poplar (Populus tremula×P. alba) trees. The en-(ALDH; EC 1.2.1.5) seems to be responsible for the oxidation zymes possibly involved in the oxidation of ethanol in the of acetaldehyde. The present results demonstrate that acetaldehyde emission is clearly dependent on its production in the leaves of trees are catalase (CAT; EC 1.11.1.6) and alcohol dehydrogenase (ADH; EC 1.1.1.1), both expressed constitu-leaves as controlled by the delivery of ethanol to the leaves via tively in the leaves of poplars. Inhibition of ADH in excised the transpiration stream. Environmental factors that control stomatal conductance seem to be of less importance for leaves caused a significant decrease of acetaldehyde emission accompanied by an increased ethanol emission. Since inhibi-acetaldehyde emission by the leaves.

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Sulphate assimilation provides reduced sulphur for the synthesis of cysteine, methionine, and numerous other essential metabolites and secondary compounds. The key step in the pathway is the reduction of activated sulphate, adenosine 5′-phosphosulphate (APS), to sulphite catalysed by APS reductase (APR). In the present study, [35S]sulphur flux from external sulphate into glutathione (GSH) and proteins was analysed to check whether APR controls the flux through the sulphate assimilation pathway in poplar roots under some stress conditions and in transgenic poplars. (i) O-Acetylserine (OAS) induced APR activity and the sulphur flux into GSH. (ii) The herbicide Acetochlor induced APR activity and results in a decline of GSH. Thereby the sulphur flux into GSH or protein remained unaffected. (iii) Cd treatment increased APR activity without any changes in sulphur flux but lowered sulphate uptake. Several transgenic poplar plants that were manipulated in sulphur metabolism were also analysed. (i) Transgenic poplar plants that overexpressed the γ-glutamylcysteine synthetase (γ-ECS) gene, the enzyme catalysing the key step in GSH formation, showed an increase in sulphur flux into GSH and sulphate uptake when γ-ECS was targeted to the cytosol, while no changes in sulphur flux were observed when γ-ECS was targeted to plastids. (ii) No effect on sulphur flux was observed when the sulphite oxidase (SO) gene from Arabidopsis thaliana, which catalyses the back reaction of APR, that is the reaction from sulphite to sulphate, was overexpressed. (iii) When Lemna minor APR was overexpressed in poplar, APR activity increased as expected, but no changes in sulphur flux were observed. For all of these experiments the flux control coefficient for APR was calculated. APR as a controlling step in sulphate assimilation seems obvious under OAS treatment, in γ-ECS and SO overexpressing poplars. A possible loss of control under certain conditions, that is Cd treatment, Acetochlor treatment, and in APR overexpressing poplar, is discussed.

Phosphorus (P) constitutes one of five macronutrients essential for plant growth and development due to the central function of phosphate in energy metabolism, inheritance and metabolic control. In many ecosystems, plant available soil-P gets limited by soil aging. Hence, plants have developed adaptation strategies to cope with such limitation by an efficient plant and ecosystem internal P-cycling during annual growth. The natural floodplain habitat of fast-growing Populus × canescens is characterized by high soil-P availability. It was thus expected that the P-nutrition of P. × canescens had adapted to this conditions. Therefore, different P-fractions in different twig tissues were investigated during two annual growth cycles. The P-nutrition of P. × canescens markedly differs from that of European beech grown at low soil-P availability (Netzer F, Schmid C, Herschbach C, Rennenberg H (2017) Phosphorus-nutrition of European beech (Fagus sylvatica L.) during annual growth depends on tree age and P-availability in the soil. Environ Exp Bot 137:194-207). This was mainly due to a lack of tree internal P-cycling during annual growth indicated by the absence of P-storage and remobilization in twig bark and wood. Hence, strategies to economize P-nutrition and to prevent P-losses had not developed. This fits with the fast-growth strategy of P. × canescens at unrestricted P-availability. Hence, the P-nutrition strategy of P. × canescens can be seen as an evolutionary adaptation to its natural growth habitat.

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Glutathione (GSH) and ascorbate (ASC) are important antioxidants that are involved in stress defence and cell proliferation of meristematic root cells. In principle, synthesis of ASC and GSH in the roots as well as ASC and GSH transport from the shoot to the roots by phloem mass flow is possible. However, it is not yet known whether the ASC and/or the GSH level in roots depends on the supply from the shoot. This was analysed by feeding mature leaves with [14C]ASC or [35S]GSH and subsequent detection of the radiolabel in different root fractions. Quantitative dependency of root ASC and GSH on shoot-derived ASC and GSH was investigated with poplar (Populus tremula×P. alba) trees interrupted in phloem transport. [35S]GSH is transported from mature leaves to the root tips, but is withdrawn from the phloem along the entire transport path. When phloem transport was interrupted, the GSH content in root tips halved within 3 d. [14C]ASC is also transported from mature leaves to the root tips but, in contrast to GSH, ASC is not removed from the phloem along the transport path. Accordingly, ASC accumulates in root tips. Interruption of phloem transport disturbed the level and the ASC redox state within the entire root system. Diminished total ASC levels were attributed mainly to a decline of dehydroascorbate (DHA). As the redox state of ASC is of particular significance for root growth and development, it is concluded that phloem transport of ASC may constitute a shoot to root signal to coordinate growth and development at the whole plant level.

This paper provides new insights into source-sink relationships and transpiration processes which will eventually help to interpret δ (18) O as a genotype selection and ecophysiological tool for maize adaptation to drought. Oxygen isotope composition (δ(18)O) has been proposed as a phenotyping tool to integrate leaf transpiration in C4 crops, such as maize. Within this context we hypothesize that δ(18)O in leaves may reflect primarily environmental and genetic variability in evaporative processes, but that this signal may become dampened in transit from source to sink tissues. The aim of this study was to assess the relative importance of transpirative or translocation-related factors affecting δ(18)O in plant tissues of maize. We performed two water regime experiments, one with two varieties under semi-controlled conditions, and another in the field with 100 genotypes during two consecutive years. The δ(18)O in organic matter at the leaf base was strongly correlated with the δ(18)O in stem water, indicating that it could be a good proxy for source water in extensive samplings. Compared to leaves, we observed an (18)O depletion in silks and grains, but not in stem-soluble organic matter. We interpret this as evidence of exchange with unenriched water from source to sink, but mainly occurring within sink tissues. Although grain yield (GY) and physiological variables did not show clear intra-trial patterns against δ(18)O, the only tissues that correlated with GY in the linear regression approach were that of silks, giving an insight of evapotranspirative demand during female flowering and thus of potential maize lines that are better adapted to drought. This finding will eventually help to interpret δ(18)O as a genotype selection and ecophysiological tool for the adaption of maize and other crops to drought, offering insight into source-sink relationships and transpiration processes.

The importance of the ectomycorrhiza symbiosis for plant acquisition of phosphorus and nitrogen is well established whereas its contribution to sulfur nutrition is only marginally understood. In a first step to investigate the role of ectomycorrhiza in plant sulfur nutrition, we characterized sulfate and glutathione uptake in Laccaria bicolor. By studying the regulation of sulfate uptake in this ectomycorrhizal fungus, we found that in contrast to bacteria, yeast, and plants, sulfate uptake in L. bicolor was not feedback-inhibited by glutathione. On the other hand, sulfate uptake was increased by sulfur starvation as in other organisms. The activity of 3'-phosphoadenosine 5'-phosphosulfate reductase, the key enzyme of the assimilatory sulfate reduction pathway in fungi, was increased by sulfur starvation and decreased after treatment with glutathione revealing an uncoupling of sulfate uptake and reduction in the presence of reduced sulfur compounds. These results support the hypothesis that L. bicolor increases sulfate supply to the plant by extended sulfate uptake and the plant provides the ectomycorrhizal fungus with reduced sulfur.