PubMed Health⌕ Search
Home/Archive/PubMed

PubMed · 12701433

Barley leaf stripe disease.

J Zad·M Aghakhani·R Etebarian·M Okhovat
View original source ↗Export metadata ↓

Abstract

Leaf stripe is one of the most important diseases of barley in Iran especially in Gorgan, Mazandran and near Tehran (Varamin). Most obvious symptoms of the disease are described. Long pale or yellow stripes become darker as the fungus sporulates on the leaf surface. Infected plants usually are stunted and produce sterile spikes, rarely a few seeds are produced. Infected spikes and late-forming tillers may produce fertile spikes. The fungus is seed brone and survives in the outer layers of infected seed. To study the seed-borne disease, we have used the different methods (ISTA). Coleoptiles of seedlings are infected by the fungus under cool, moist conditions, a soil temperature below 15 degrees C is necessary for seed infection. The fungus penetrates through coleoptiles and grows systemically within the plant, produces toxin and kills cells and discolors leaf tissue between veins, thus causing striped lesions. When conditions are wet or humid, spores are produced on the surface of leaves at above the time spikes of healthy plant. Morphological characteristics of the vegetative and reproductive structures of the fungus show that it is Drechslera graminea (Rabenh) Shoemaker.

Explore related subjects

CotyledonFertilityHordeumIranMitosporic FungiPlant DiseasesPlant LeavesSpores, FungalJournal Article

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J Zad, M Aghakhani, R Etebarian, M Okhovat. 2002. Barley leaf stripe disease.. https://pubmed.ncbi.nlm.nih.gov/12701433/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

PubMed2025

A PIF-regulated switch in cell axis growth drives cotyledon expansion through tissue-specific cell expansion and division.

Despite its crucial role during seedling deetiolation, cotyledon expansion has been largely overlooked, with hypocotyl elongation favored as the primary phenotypic readout in light signaling research. Here, we investigate how cotyledon expansion is regulated during seedling establishment and reveal that light-induced cotyledon expansion involves a rapid switch in growth direction - from longitudinal in darkness to transversal upon initial light exposure. Using PIFq- and phyA/phyB-deficient Arabidopsis mutants, we demonstrate that this switch is repressed by PIFs in the dark and promoted by phytochromes under red light. Notably, expansion is antagonistically regulated in the light by GUN1-mediated plastid retrograde signaling. Cotyledon expansion involves rapid epidermis cell expansion, transitioning from rectangular in darkness to characteristic lobed cells in light. Importantly, our findings show that mesophyll extension is driven not only by cell enlargement but also by palisade cell division, consistent with an enrichment of cell cycle-related genes that are antagonistically regulated by the PIF/phy system and retrograde signaling in the cotyledon. Finally, using mutant lines expressing PIF1 and phyB specifically in the epidermis, we establish that epidermal expansion can drive palisade cell growth, while mesophyll cell division is predominantly regulated by light at the tissue-specific level. This study provides a novel framework for investigating cotyledon expansion during seedling deetiolation, incorporating tissue-level regulation. We propose that cotyledons serve as an excellent model for studying morphogenesis and organ geometry, which in plants is governed by directional cell growth.

Cotyledon↗
PubMed2007

Protein storage vacuole acidification as a control of storage protein mobilization in soybeans.

Soybean protease C1 (EC 3.4.21.25), the subtilisin-like serine protease that initiates the proteolysis of seed storage proteins in germinating soybean [Glycine max (L.) Merrill], was localized to the protein storage vacuoles of parenchyma cells in the cotyledons by immunoelectron microscopy. This was demonstrated not only in germination and early seedling growth as expected, but also in two stages of protein storage vacuole development during seed maturation. Thus, the plant places the proteolytic enzyme in the same compartment as the storage proteins, but is still able to accumulate those protein reserves. Since soybean protease C1 activity requires acidic conditions for activity, the hypothesis that the pH condition in the protein storage vacuole would support protease C1 activity in germination, but not in seed maturation, was tested. As hypothesized, acridine orange accumulation in the protein storage vacuole of storage parenchyma cells was detected by fluorescence confocal microscopy in seedlings before the onset of mobilization of reserve proteins as noted by SDS-PAGE. Accumulation of the dye was reversed by inclusion of the weak base methylamine to dissipate the pH gradient across the vacuolar membrane. Also as hypothesized, acridine orange did not accumulate in the protein storage vacuole of those parenchyma cells during seed maturation. These results were obtained using cells separated by pectolyase treatment and also using cotyledon slices.

Cotyledon↗
PubMed2006

Patterns and kinetics of water uptake by soybean seeds.

Soybean [Glycine max (L.) Merr.] plants produce some seeds (called stone or impermeable seeds) that do not take up water for long periods of time. The present investigation confirmed that the stone seed trait is a feature of the seed coat: isolated embryos from both stone and permeable seeds took up water equally quickly. A whole, permeable seed typically imbibed water initially through its dorsal side, forming wrinkles in the seed coat and delivering water to the underlying cotyledons. Later, some lateral movement of water through the coat occurred, presumably through the air spaces of the osteosclereid layer. Imbibition by seeds was a two-phase process, the first dominated by hydration of the seed coat and the second by hydration of the cotyledons, which was rate-limited by the coat. When hydrated, coats of stone seeds were permeable to water but their hydraulic conductivity, as measured with a pressure probe, was smaller than that of coats from permeable seeds by a factor of five. Hydrated coats of both permeable and stone seeds showed weak osmometer properties.

Cotyledon↗