The relationship between guard cell water potential and the aperture of stomata in Populus

Abstract Previous work with clones of Populus trichocarpa demonstrated that the water vapour conductance of leaves from well-watered cuttings of this species does not decline with loss of turgor from the bulk leaf. In the present study, stomatal responses to water potential in Populus were examined with detached epidermal strips. Stomata in epidermal strips from well-watered plants of P. trichocarpa did not close at low water potentials which led to plasmolysis of the guard cells. In contrast, stomata of P. deltoides and a P. trichocarpa×deltoides hybrid closed when the guard cells lost turgor. A period of water stress preconditioning resulted in modified stomatal responses in P. trichocarpa such that stomata of stressed and re-watered plants nearly closed when guard cell turgor was lost.     

An alternative approach for gene transfer in trees using wild-typeAgrobacterium strains

Micropropagated shoots of three forest tree species, poplar (Populus tremula × P.alba), wild cherry (Prunus avium L.) and walnut (Juglans nigra × J. regia), were inoculated each with six different wild-typeAgrobacterium strains. Poplar and wild cherry developed tumors that grew hormone-independently, whereas on walnut, gall formation was weak. On poplar and wild cherry, tumors induced by nopaline strains developed spontaneously shoots that had a normal phenotype and did not carry oncogenic T-DNA. From these observations, we have established a co-inoculation method to transform plants, using poplar as an experimental model. The method is based on inoculation of stem internodes with anAgrobacterium suspension containing both an oncogenic strain that induces shoot differentiation and a disarmed strain that provides the suitable genes in a binary vector. We used the vector pBI121 carryingneo (kanamycin resistance) anduidA (-glucuronidase) genes to facilitate early selection and screening. Poplar plants derived from kanamycin-resistant shoots that did not carry oncogenic T-DNA, were shown to contain and to expressneo anduidA genes. These results suggest that wild-typeAgrobacterium strains that induce shoot formation directly from tumors can be used as a general tool for gene transfer, avoiding difficult regeneration procedures.This work is dedicated to the late Marie-France Michel who initiated the poplar biotechnology project at INRA.     

Records on parasitoids of smaller poplar borer,Saperda populnea [Coleoptera,Cerambycidae] along the Danube in Bulgaria

During the period 1986–1988 the parasitoids of smaller poplar borer,Saperda populnea L. (Coleoptera, Cerambycidae) along the Danube in Bulgaria were studied. A total of 898 smaller poplar borer galls were investigated—289 in 1986, 404 in 1987, and 205 in 1988. In the particular years the parasitoids of smaller poplar borer namelyBillaea irrorata Meig.(Diptera, Tachinidae), Dolichomitus populneus Ratz. (Hym.: Ichneumonidae), andIphiaulax impostor Scop. (Hym.: Braconidae) destroyed from 13.1 up to 28.0% of the pest larvae, thus decreasing their frequency together with the other limiting factors by 56.1% up to 81.2%. The tachinid flyB. irrorata decreased the smaller poplar borer larvae frequency by 9.3% up to 18.9%, while the ichneumonoidD. populneus, and the braconoidI. impostor destroyed insignificant percentages of these larvae—0.5% up to 1.7% and 0.5% up to 2.5% resp. The flight period of the pest preceded or almost coincided with the ones ofD. populneus, andI. impostor. The flyB. irrorata always appeared last and its flight period was expanded.      

Choosing tree genotypes for phytoremediation of landfill leachate using phyto-recurrent selection

Information about the response of poplar (Populus spp.) genotypes to landfill leachate irrigation is needed, along with efficient methods for choosing genotypes based on leachate composition. Poplar clones were irrigated during three cycles of phyto-recurrent selection to test whether genotypes responded differently to leachate and water, and to test whether the methodology had merit as a tool for plant selection during remediation. Fifteen below- and above-ground traits were evaluated. Twenty-five clones were tested in cycle 1, while the best l2 genotypes were evaluated in cycles 2 and 3. Eight clones were selected and subsequently tested in an in situ landfill study (cycle 4). Results from cycles 1, 2, and 3 are presented here. Overall, clones responded differently to irrigation treatments, with certain genotypes exhibiting better below- and above-ground growth with water than leachate. However, growth was greater with leachate irrigation for some clones. In addition, differences between treatments within clones decreased with days after planting (DAP). There were no treatment differences for number of leaves, height, and root length at the end of cycle 2 (45 DAP) or cycle 3 (30 DAP). These results detail the extensive variation in clonal responses to leachate irrigation, along with the need and efficacy of using phyto-recurrent selection to choose superior genotypes.     

盐胁迫对不同品系杨树幼苗生长、细胞超微结构和离子稳态的影响

以欧美杨（Populus canadensis）南杨1号和南杨2号为实验材料,研究了NaCl胁迫对其幼苗生长、细胞超微形态结构和离子分配等的影响。结果发现,低盐（75mmol·L^–1NaCl）胁迫对南杨1号生长的抑制显著高于南杨2号;高盐（150mmol·L^–1NaCl）胁迫对2种品系生长的抑制则差异不显著。低盐胁迫下,南杨1号叶片细胞结构破坏程度明显高于南杨2号;南杨2号根中所有细胞,新生枝条表皮、皮层及木质部细胞,叶片上表皮、栅栏和海绵组织细胞均维持较低的Na＋含量,同时叶片栅栏和海绵组织细胞维持较高的Mg2＋含量,从而表现为向枝条和叶片的Na＋流量显著偏低。维持细胞内的离子稳态可能是南杨2号耐盐性高于南杨1号的重要原因。     

Evaluation of heterologous promoters in transgenic Populus tremula × P. alba plants

The pattern and expression level of β-glucuronidase (gus) reporter gene regulated by six heterologous promoters were studied in transgenic Populus tremula × P. alba plants obtained by Agrobacterium-mediated transformation. Binary vector constructs used contained the following promoter sequences: the CaMV35S from cauliflower mosaic virus; its duplicated version fused to the enhancer sequence from alfalfa mosaic virus; CsVMV from cassava vein mosaic virus; ubiquitin 3 from Arabidopsis thaliana (UBQ3); S-adenosyl-L-methionine synthetase (Sam-s) from soybean; and the rolA from Agrobacterium rhizogenes. Histochemical staining of root, stem and leaf tissues showed phloem and xylem-specific gus expression under rolA promoter, and constitutive expression with the other putative constitutive promoters. Quantitative GUS expression of 10 – 15 independently transformed in vitro grown plants, containing each promoter, was determined by fluorimetric GUS assays. The UBQ3-gus fusion induced the highest average expression level, although an extensive variation in expression levels was observed between independent transgenic lines for all the constructs tested.     

Regulation of sulfate assimilation in Arabidopsis and beyond

BACKGROUND AND AIMS: Sulfate assimilation is a pathway used by prokaryotes, fungi and photosynthetic organisms to convert inorganic sulfate to sulfide, which is further incorporated into carbon skeletons of amino acids to form cysteine or homocysteine. The pathway is highly regulated in a demand-driven manner; however, this regulation is not necessarily identical in various plant species. Therefore, our knowledge of the regulation of sulfate assimilation is reviewed here in detail with emphasis on different plant species. SCOPE: Although demand-driven control plays an essential role in regulation of sulfate assimilation in all plants, the molecular mechanisms of the regulation and the effects of various treatments on the individual enzymes and metabolites are often different. This review summarizes (1) the molecular regulation of sulfate assimilation in Arabidopsis thaliana, especially recent data derived from platform technologies and functional genomics, (2) the co-ordination of sulfate, nitrate and carbon assimilations in Lemna minor, (3) the role of sulfate assimilation and glutathione in plant-Rhizobia symbiosis, (4) the cell-specific distribution of sulfate reduction and glutathione synthesis in C(4) plants, (5) the regulation of glutathione biosynthesis in poplar, (6) the knock-out of the adenosine 5'phosphosulfate reductase gene in Physcomitrella patens and identification of 3'-phosphoadenosyl 5'-phosphosulfate reductase in plants, and (7) the sulfur sensing mechanism in green algae. CONCLUSIONS: As the molecular mechanisms of regulation of the sulfate assimilation pathway are not known, the role of Arabidopsis as a model plant will be further strengthened. However, this review demonstrates that investigations of other plant species will still be necessary to address specific questions of regulation of sulfur nutrition.