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Plant growth-promoting bacteria confer resistance in tomato plants to salt stress.

The object of the work is to evaluate whether rhizobacteria populating dry salty environments can increase resistance in tomato to salt stress. Seven strains of plant growth-promoting bacteria that have 1-aminocyclopropane-1-carboxylate (ACC) deaminase activity were isolated from soil samples taken from the Arava region of southern Israel. Following growth of these seedlings in the presence of 43 mM NaCl for 7 weeks, the bacterium that promoted growth to the greatest extent was selected for further study. DNA analysis of the 16S RNA indicated that the selected bacterium was Achromobacter piechaudii. This bacterium significantly increased the fresh and dry weights of tomato seedlings grown in the presence of up to 172 mM NaCl salt. The bacterium reduced the production of ethylene by tomato seedlings, which was otherwise stimulated when seedlings were challenged with increasing salt concentrations, but did not reduce the content of sodium. However, it slightly increased the uptake of phosphorous and potassium, which may contribute in part to activation of processes involved in the alleviation of the effect of salt. In the presence of salt the bacterium increased the water use efficiency (WUE). This may suggest that the bacterium act to alleviate the salt suppression of photosynthesis. However, the detailed mechanism was not elucidated. The work described in this report is a first step in the development of productive agricultural systems in saline environments.

Achromobacter↗

Plant small nuclear RNAs. II. U6 RNA and a 4.5SI-like RNA are present in plant nuclei.

Two small nuclear RNA species (U6 RNA and a 4.5SI-like RNA) not described so far for plants were detected in broad bean (Vicia faba L.) nuclei. U6 RNA is 98 nucleotides long, contains psi and methylated nucleotides and shows a surprisingly high degree of sequence homology (80%) with its rat counterpart, particularly in the middle part (a 57 nucleotide-long stretch) of the molecule, where it amounts to 98%. The 4.5SI-like RNA, similar in its structure to 4.5SI RNA detected so far only in rodent nuclei, is 94 nucleotides long, contains psi and an unidentified nucleotide and exhibits 52% overall sequence homology with rat 4.5SI RNA. A block of 20 consecutive nucleotides at the 5' end of the molecule is conserved between broad bean 4.5SI-like RNA and rat 4.5SI RNA. The presence of the two RNA polymerase III internal promoter consensus sequences in 4.5SI-like RNA suggests that it is an RNA polymerase III transcript.

Animals↗

The transcriptional activation domain of the plant-specific Dof1 factor functions in plant, animal, and yeast cells.

Maize Dof1, one of the plant-specific Dof transcription factors, is involved in light-regulated gene expression. To elucidate the molecular mechanism underlying the activity of Dof1, in vivo functional analyses were carried out using transient expression assays with maize mesophyll protoplasts. The results suggest that the Dof domain alone, the region conserved among Dof factors, can mediate interaction with DNA in vivo and distinct Dof1 activities in greening and etiolated protoplasts. A region rich in basic amino acids was identified as a nuclear localization signal. Deletion analysis defined the transcriptional activation domain of 48 amino acids located in the C-terminus of Dof1. This activation domain was also found to be functional in both human cells and yeast, implying that Dof1 may stimulate transcription through a mechanism evolutionarily conserved among eukaryotes. A computer homology search with known transcription factors revealed that the activation domain of Dof1 displayed only a limited similarity to Activation domain II of animal transcription factor GATA-4. Mutational analysis revealed the critical role of a tryptophan residue within the activation domain of Dof1, as had been shown in Activation domain II of GATA-4.

Amino Acid Sequence↗

Differential accumulation of plant defense gene transcripts in a compatible and an incompatible plant-pathogen interaction.

Phenylalanine ammonia-lyase and chalcone synthase catalyze the first reaction of phenylpropanoid biosynthesis and the first reaction of a branch pathway specific for flavonoid-isoflavonoid biosynthesis, respectively. These enzymes are key control elements in the synthesis of kievitone, phaseollin, and related isoflavonoid-derived phytoalexins. RNA blot hybridization with 32P-labeled cDNA sequences was used to demonstrate marked accumulation of phenylalanine ammonia-lyase and chalcone synthase mRNAs in excision-wounded hypocotyls of Phaseolus vulgaris L. (dwarf French bean) and during race-cultivar-specific interactions between hypocotyls of P. vulgaris and the partially biotrophic fungus Colletotrichum lindemuthianum, the causal agent of anthracnose. In an incompatible interaction (host resistant), early concomitant accumulation of phenylalanine ammonia-lyase and chalcone synthase mRNAs, localized mainly but not entirely in tissue adjacent to the site of infection, was observed prior to the onset of phytoalexin accumulation and expression of localized, hypersensitive resistance. In contrast, in a compatible interaction (host susceptible) there was no early accumulation of these transcripts; instead, there was a delayed widespread response associated with phytoalexin accumulation during attempted lesion limitation. Two-dimensional gel electrophoresis of [35S]methionine-labeled polypeptides synthesized in vitro by translation of isolated polysomal RNA demonstrated stimulation of the synthesis of characteristic sets of phenylalanine ammonia-lyase and chalcone synthase isopolypeptides in directly infected tissue and distant, hitherto uninfected tissue in both compatible and incompatible interactions. Our data show that specific accumulation of plant defense gene transcripts is a key early component in the sequence of events leading to expression of defense responses in wounded tissue and in infected tissue during race-cultivar-specific interactions and that an elicitation signal is transmitted intercellularly in response to infection.

Base Sequence↗

Antiproliferative constituents in Umbelliferae plants II. Screening for polyacetylenes in some Umbelliferae plants, and isolation of panaxynol and falcarindiol from the root of Heracleum moellendorffii.

Methanol extracts of 36 samples of 21 Umbelliferae plants were screened for polyacetylenic compounds using the ELISA for panaxytriol, and their antiproliferative activity was checked by MTT assay using the tumor cell lines MK-1, HeLa and B16F10. The presence of antiproliferative polyacetylenes was suggested in Angelica acutiloba (fruit), Anethum graveolens (root), Bupleurum rotundifolium (fruit), Carum carvi (fruit and root), Coriandrum sativum (fruit), Cryptotaenia japonica (leaf), Glehnia littoralis (fruit), Heracleum moellendorffii (root) and Torilis japonica (fruit). Panaxynol and falcarindiol were successfully isolated from the root of Heracleum moellendorffii as antiproliferative polyacetylenes.

Acetylene↗

Plant compositional constituents affecting between-plant and animal species prediction of forage intake.

The purpose of the study was to identify plant compositional constituents that influence forage intake. Emphasis was put on the ratio in vitro digestibility of organic matter (IVDOM):NDF because preliminary work with cattle and a limited number of forages showed the ratio to account for more variation in intake than either IVDOM or NDF alone. The compositional constituents were tested in intake prediction models using local and published data (n = 302) on grass pastures, silages, hays, straws, legumes, grass-legume mixtures, and shrubs ingested by both browsing and grass-eating ruminants (goats, red deer, impala, blesbok, sheep, cattle, and blue wildebeest). In the local experiments, esophageally fistulated and fecal bag-harnessed animals were used to collect representative grazed forage samples from pastures and to determine OM excreted, respectively. Forage intake was calculated as OM excreted divided by (1-IVDOM). Intake of silages, hays, and straws was measured indoors in digestibility trials. Intakes among species were compared after scaling for size by BW raised to the power of .9. Major contributors to the variation in forage intake were ash, hemicellulose, IVDOM:NDF, ADL, and the interaction between DM content and, respectively, ash, N, and ADL. High tannin/phenol concentrations proved limiting to intake. The ratio of IVDOM:NDF accounted for 67% of the variation in forage intake if data for which the other constituents had an effect were omitted, and the equation, OMI, g.kg BW-.9.d-1 = 70-97e-.975(IVDOM:NDF), predicted intake across all forages and ruminant species with a Sy.x of 5.3 g.kg BW-.9.d-1 (CV = 15%). The ratio of IVDOM:NDF should be valuable as a relatively inexpensive and rapid method to screen forages and cultivars.

Animals↗

Investigation of molluscicidal activity of certain Sudanese plants used in folk-medicine. I. A preliminary biological screening for molluscicidal activity of certain Sudanese plants used in folk-medicine.

A preliminary biological screening for molluscicidal activity of certain Sudanese plants used in Folk-medicine was carried out. 78 samples belonging to 51 species, 45 genera and 28 families were screened. The aqueous extracts of 18 samples belonging to 8 species, 6 genera and 5 families were found to be active against Bulinus truncatus and 7 of these were also found to be active against Biomphalaria pfeifferi. Successive extraction of the 18 active samples with petroleum ether, ethanol and water showed that the petroleum ether extracts of only 4 samples were active against Bulinus truncatus; while the alcoholic extracts of 16 samples were found to be active against the same snail species. Only the alcoholic extracts of 4 samples were proved to be active against Biomphalaria pfeifferi. In the successive extraction technique, only the aqueous extract of Gardenia vogelii fruit pulp was proved to be active against the two snail species tested.

Acacia↗

[Chlorophyll-protein complexes from green algae and higher plants. Heterogeneity of chloroplast complexes from dimorphous tissue of C4 plant leaves].

It was demonstrated that the decrease of the activity of photosystem II in agranal chloroplasts of bundle sheath cells of malate C4 plants is due to a loss of the chlorophyll-protein complex of this photosystem. This is paralleled with an increase in the relative amount of the chlorophyll--protein complex of photosystem I and a partial loss of the light-harvesting pigmentprotein complex. These two events may account for the high activity of photosystem I and for the low content of chlorophyll b in the plastids. The cumulative data are indicative of a close interrelationship between the granal state of the chloroplast membranes and the presence of the chlorophyll--protein complex of photosystem II.

Chlorophyll↗

Plant sterol biosynthesis: identification and characterization of higher plant delta 7-sterol C5(6)-desaturase.

Microsomes obtained from maize seedlings catalyzed the introduction of the delta5-bond into delta7-sterols to yield the corresponding delta 5,7-sterols. Enzymatic bioassay conditions have been developed for the first time for delta 7-sterol C5(6)-desaturase in photosynthetic organisms. The properties of the microsomal system have been studied and the kinetics of the desaturation reaction has been established. The desaturation reaction requires molecular oxygen and NADH. Coenzyme efficiency studies indicate that NADH is more efficient that NADPH and that in the presence of NADH, NAD+ stimulates the desaturation process but cannot sustain the reaction by itself. The desaturation is strongly inhibited by cyanide, is sensitive to 1,10-phenanthroline and to salicylhydroxamic acid, but is insensitive to carbon monoxide, suggesting the involvement of a metal ion, presumably iron, in an enzyme-bound form in the desaturating system. From a series of incubations with delta 7-sterols and other sterol analogs, the substrate specificity for desaturation was determined. Our data indicate the substrate selectivity of the C5(6)-desaturation for 4-desmethyl-delta 7-sterols. Moreover, the results show that specificity of maize C5(6)-desaturase favored delta 7-sterols possessing a C24-methylene or ethylidene substituent compared to 24-ethyl-substituted delta 7-sterols. Finally, the results demonstrate directly that during plant sterol synthesis the delta 5-bond is introduced via the sequence delta 7-sterol-->delta 5,7-sterol-->delta 5-sterol.

Coenzymes↗

[Pesticide residues in food plants: the role of plant metabolism].

The plant metabolism of pesticides typically leads to various classes of persistent "soluble" and "insoluble" conjugates whose structures and modes of formation and storage have been characterized only in recent years. Pesticide risk assessment should include studies on animal bioavailability and toxicological properties of the conjugates.

Animals↗

Plant cyanogenesis of Phaseolus lunatus and its relevance for herbivore-plant interaction: the importance of quantitative data.

Quantitative experimental results on the antiherbivorous effect of cyanogenesis are rare. In our analyses, we distinguished between the total amount of cyanide-containing compounds stored in a given tissue [cyanogenic potential (HCNp)] and the capacity for release of HCN per unit time (HCNc) from these cyanogenic precursors as a reaction to herbivory. We analyzed the impact of these cyanogenic features on herbivorous insects using different accessions of lima beans (Phaseolus lunatus L.) with different cyanogenic characteristics in their leaves and fourth instars of the generalist herbivore Schistocerca gregaria Forskål (Orthoptera, Acrididae). Young leaves exhibit a higher HCNp and HCNc than mature leaves. This ontogenetic variability of cyanogenesis was valid for all accessions studied. In no-choice bioassays, feeding of S. gregaria was reduced on high cyanogenic lima beans compared with low cyanogenic beans. A HCNp of about 15 micromol cyanide/g leaf (fresh weight) with a corresponding HCNc of about 1 micromol HCN released from leaf material within the first 10 min after complete tissue disintegration appears to be a threshold at which the first repellent effects on S. gregaria were observed. The repellent effect of cyanogenesis increased above these thresholds of HCNp and HCNc. No repellent action of cyanogenesis was observed on plants with lower HCNp and HCNc. These low cyanogenic accessions of P. lunatus were consumed extensively--with dramatic consequences for the herbivore. After consumption, locusts showed severe symptoms of intoxication. Choice assays confirmed the feeding preference of locusts for low over high cyanogenic leaf material of P. lunatus. The bioassays revealed total losses of HCN between 90 and 99% related to the estimated amount of ingested cyanide-containing compounds by the locusts. This general finding was independent of the cyanogenic status (high or low) of the leaf material.

Animals↗

Inventory of plants used in traditional medicine in Tanzania. I. Plants of the families Acanthaceae-Cucurbitaceae.

Sixty-two plants are listed, which are used by traditional healers in the northeastern part of Tanzania. For each species are given: the botanical name with synonyms, vernacular name, collection number, locality, habitus, approximate distribution, and medical use. Results of a literature survey are also reported, including medical use, isolated constituents and pharmacological effects.

Humans↗

Inventory of plants used in traditional medicine in Tanzania. II. Plants of the families Dilleniaceae--Opiliaceae.

Forty five plants are listed, which are used by traditional healers in the northeastern part of Tanzania. For each species are given: the botanical name with synonyms, vernacular name, collection number, locality, habitus, approximate distribution and medical use. Results of a literature survey are also reported, including medical use, isolated constituents and pharmacological effects.

Humans↗

Inventory of plants used in traditional medicine in Tanzania. Part III. Plants of the families Papilionaceae-Vitaceae.

Forty-six plants are listed, which are used by traditional healers in the northeastern part of Tanzania. For each species are given: the botanical name with synonyms; vernacular name; collection number; locality; habitus; approximate distribution and medical use. Results of a literature survey are also reported, including medical use, isolated constituents and pharmacological effects.

Phytotherapy↗

Inventory of plants used in traditional medicine in Somalia. I. Plants of the families Acanthaceae-Chenopodiaceae.

Thirty-eight plants are listed, which are used by traditional healers in the central and southern parts of Somalia. For each species are listed: the botanical name with synonyms, collection number, vernacular name, medicinal use, preparation of remedy and dosage. Results of a literature survey are also reported including medicinal use, substances isolated and pharmacological effects.

Animals↗

Inventory of plants used in traditional medicine in Somalia. II. Plants of the families Combretaceae to Labiatae.

Fifty-nine plants are listed, which are used by traditional healers in the central and southern parts of Somalia. For each species are listed: the botanical name with synonyms, collection number, vernacular name, medicinal use, preparation of remedy and dosage. Results of a literature survey are also reported including medicinal use, substances isolated and pharmacological effects.

Medicine, Traditional↗

Inventory of plants used in traditional medicine in Somalia. III. Plants of the families Lauraceae-Papilionaceae.

Thirty-five plants are listed, which are used by traditional healers in the central and southern parts of Somalia. For each species are listed: the botanical name with synonyms, collection number, vernacular name, medicinal use, preparation of remedy and dosage. Results of a literature survey are also reported including medicinal use, substances isolated and pharmacological effects.

Humans↗