Barley aleurone xylanase: its biosynthesis and possible role

1989 ◽  
Vol 67 (2) ◽  
pp. 297-302 ◽  
Author(s):  
E. Benjavongkulchai ◽  
M. S. Spencer
Keyword(s):  
Electron Microscopy ◽  
Cell Walls ◽  
De Novo ◽  
Xylanase Activity ◽  
Hordeum Vulgare L ◽  
Aleurone Cells ◽  
Initial Release ◽  
Barley Aleurone ◽  
Scanning Electron

The synthesis of barley (Hordeum vulgare L. cv. Himalaya) aleurone xylanase was found to be dependent on both gibberellic acid (GA3) and Ca2+, but inhibited by cycloheximide and cordycepin. Studies using density labeling of barley aleurone layers showed that xylanase was synthetized de novo in response to GA3 and Ca2+. Neither GA3 nor Ca2+ alone induced a large increase in xylanase activity. The concentration of Ca2+ required for maximum xylanase induction was 5 – 40 mM. Xylanase activity was found to develop simultaneously with that of α-amylase in the incubation medium during the first 24 h of incubation with GA3. A critical point with respect to the role of xylanase is the extent of its activity by the time of the initial release of α-amylase. The release of α-amylase into the medium was detectable at 6 h. From 2 to 6% of the cell wall was hydrolysed by xylanase after incubation for 6 h, which was probably sufficient to permit the release of α-amylase. Scanning electron microscopy showed that the purified barley aleurone xylanase hydrolysed the cell walls of barley aleurone layers in the absence of GA3. It is likely that xylanase plays an important role in the release of enzymes from aleurone cells.

The use of scanning electron microscopy in interpreting chenopodium remains from three archaeological sites in northwestern Iowa

1992 ◽  
Vol 50 (2) ◽  
pp. 1112-1113
Author(s):  
Douglas William Jones
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Archaeological Sites ◽  
Late Prehistoric ◽  
Eastern United States ◽  
Chenopodium Berlandieri ◽  
Seed Identification ◽  
Level 2 ◽  
Scanning Electron

Within the past 20 years, archaeobotanical research in the Eastern United States has documented an early agricultural complex before the dominance of the Mesoamerican domesticates (corn, beans, and squash) in late prehistoric and historic agricultural systems. This early agricultural complex consisted of domesticated plants such as Iva annua var.macrocarpa (Sumpweed or Marshelder), Hellanthus annuus (Sunflower) and Chenopodium berlandieri, (Goosefoot or Lasbsquarters), and heavily utilized plants such as Polygonum erectum (Erect Knotweed), Phalaris caroliniana (May grass), and Hordeum pusillum (Little Barley).Recent research involving the use of Scanning Electron Microscopy (SEM) specifically on Chenopodium has established diagnostic traits of wild and domesticated species seeds. This is important because carbonized or uncarbonized seeds are the most commonly recovered Chenopodium material from archaeological sites. The diagnostic seed traits assist archaeobotanists in identification of Chenopodium remains and provide a basis for evaluation of Chenopodium utilization in a culture's subsistence patterns. With the aid of SEM, an analysis of Chenopodium remains from three Late Prehistoric sites in Northwest Iowa (Blood Run [Oneota culture], Brewster [Mill Creek culture], and Chan-Ya-Ta [Mill Creek culture]) has been conducted to: 1) attempt seed identification to a species level, 2) evaluate the traits of the seeds for classification as either wild or domesticated, and 3) evaluate the role of Chenopodium utilization in both the Oneota and Mill Creek cultures.

Study of Phosphocalcic Glasses from SiO2-CaO-P2O5 System with and Without Silver II. The bioactivity analysis by FTIR, SEM methods and microbiological study of silver-doped glasses

2017 ◽  
Vol 68 (6) ◽  
pp. 1188-1192
Author(s):  
Daniela Avram ◽  
Nicolae Angelescu ◽  
Dan Nicolae Ungureanu ◽  
Ionica Ionita ◽  
Iulian Bancuta ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Body Fluid ◽  
Pathogenic Bacteria ◽  
De Novo ◽  
Microbiological Examination ◽  
Doped Glasses ◽  
P2o5 System ◽  
Scanning Electron

The study in vitro of the glass powders bioactivity was performed by soaking them in simulated body fluid for 3 to 21 days at a temperature of 37�C and pH = 7.20. The synthesis de novo of hydroxyapatite, post soaking was confirmed by Fourier Transform Infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The study of the antimicrobial activity was performed by microbiological examination on two strains of pathogenic bacteria involved in postoperative nosocomial infections.

Actinomycetes in discolored wood of living silver maple

1981 ◽  
Vol 59 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Robert A. Blanchette ◽  
John B. Sutherland ◽  
Don L. Crawford
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Carbon Source ◽  
Cell Walls ◽  
Hydroxybenzoic Acid ◽  
Liquid Media ◽  
Streptomyces Strain ◽  
Culture Techniques ◽  
Silver Maple ◽  
Scanning Electron

The greenish-brown margin of discolored wood in three living silver maple trees, Acer saccharinum L., was examined by scanning electron microscopy and microbiological culture techniques. Micrographs of xylem vessels revealed filamentous structures; some of them appeared to be actinomycetous hyphae. Actinomycetes identified as Streptomyces parvullus Waksman & Gregory, S. sparsogenes Owen, Dietz & Camiener, and a third Streptomyces strain were isolated repeatedly from discolored wood of each tree. These isolates grew in liquid media in the presence of 0.1% (w/v) concentrations of several phenols. Although other phenols included in the test were not substantially degraded, p-hydroxybenzoic acid was utilized as a carbon source by S. parvullus. All three actinomycetes inhibited growth of selected wood-inhabiting fungi when paired on malt agar. When inoculated on sterilized sapwood and discolored wood from silver maple, the actinomycetes colonized vessel walls and occlusions, but were not observed to decay cell walls.

Review — The Orientation of Cellulose Microfibrils in the cell walls of Tracheids in Conifers

IAWA Journal ◽  
2005 ◽  
Vol 26 (2) ◽  
pp. 161-174 ◽  
Author(s):  
Hisashi Abe ◽  
Ryo Funada
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Outer Layer ◽  
Cell Walls ◽  
Secondary Wall ◽  
Middle Layer ◽  
Cellulose Microfibrils ◽  
Conifer Species ◽  
Predominant Orientation ◽  
Scanning Electron

We examined the orientation of cellulose microfibrils (Mfs) in the cell walls of tracheids in some conifer species by field emission-scanning electron microscopy (FE-SEM) and developed a model on the basis of our observations. Mfs depositing on the primary walls in differentiating tracheids were not well-ordered. The predominant orientation of the Mfs changed from longitudinal to transverse, as the differentiation of tracheids proceeded. The first Mfs to be deposited in the outer layer of the secondary wall (S1 layer) were arranged as an S-helix. Then the orientation of Mfs changed gradually, with rotation in the clockwise direction as viewed from the lumen side of tracheids, from the outermost to the innermost S1 layer. Mfs in the middle layer of the secondary wall (S2 layer) were oriented in a steep Z-helix with a deviation of less than 15° within the layer. The orientation of Mfs in the inner layer of the secondary wall (S3 layer) changed, with rotation in a counterclockwise direction as viewed from the lumen side, from the outermost to the innermost S3 layer. The angle of orientation of Mfs that were deposited on the innermost S3 layer varied among tracheids from 40° in a Z-helix to 20° in an S-helix.

Effect of Zn on the intermetallics formation and reliability of Sn-3.5Ag solder on a Cu pad

2007 ◽  
Vol 22 (7) ◽  
pp. 1879-1887 ◽  
Author(s):  
Y.K. Jee ◽  
Y.H. Ko ◽  
Jin Yu
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Isothermal Aging ◽  
X Ray Diffraction ◽  
X Ray ◽  
Drop Tests ◽  
Joint Microstructures ◽  
Role Of Zn ◽  
Scanning Electron

Varying amounts of Zn (1, 3, and 7 wt%) were added to Sn–3.5Ag solder on a Cu pad, and the resultant solder joint microstructures after a reflow and isothermal aging (150 °C, up to 500 h) were investigated using scanning electron microscopy, energy dispersive x-ray, and x-ray diffraction, which were subsequently correlated to the results of microhardness and drop tests. Zinc was effective in improving the drop resistance of Sn–3.5Ag solder on the Cu pad, and an addition of 3 wt% Zn nearly doubled the number of drops-to-failure (Nf). The beneficial role of Zn was ascribed to suppression of Cu6Sn5 and precipitation of Zn-containing intermetallic compounds (IMCs). However, the Zn effect was reduced as Cu6Sn5 and Ag3Sn precipitated in a joint IMC layer after prolonged aging. The interface between Ag5Zn8 and Cu5Zn8 was resistant to drop impact, but two other layered IMC structures of Cu6Sn5/Cu3Sn and Cu5Zn8/Cu6Sn5 were not.

Effect of Seedings on the Microstructure of Hydrated Alumina

2012 ◽  
Vol 554-556 ◽  
pp. 709-713
Author(s):  
Yan Hong Liu ◽  
Hong Wen Ma ◽  
Mei Tang Liu
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Decisive Role ◽  
Mechanism Study ◽  
Hydrated Alumina ◽  
Crystal Nucleus ◽  
X Ray ◽  
Intrinsic Mechanism ◽  
Scanning Electron

The morphology and particle size of boehmite play a decisive role on the application of alumina that derived from it. In this paper, we employed pseudoboehmite that produced from Al2 (SO4)3•18H2O and NH3•H2O at 70 °C, pH 7.5 as precursor to synthesize boehmite, and utilized different seeding when preparing pseudoboehmite and boehmite. To identify the influence of seeding on the microstructure of pseudoboehmite and boehmite, the products were characterized by X-ray powder diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and BET. The results indicate that the pseudoboehmite seeding has a significant influence on the morphology and particle size of pseudoboehmite to which we should pay high attention. However, the boehmite seeding does not play the role of crystal nucleus as expected. The further intrinsic mechanism study is ongoing.

scholarly journals Anatomía de la semilla de Tigridia pavonia (Iridaceae)

2017 ◽  
pp. 66
Author(s):  
Aída Carrillo-Ocampo ◽  
E.M. Engleman
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Light Microscopy ◽  
Thin Layer ◽  
Cell Walls ◽  
Histochemical Staining ◽  
Stage Of Development ◽  
Scanning Electron

With methods of light microscopy, histochemical staining and scanning electron microscopy, it was found that the ovule in the seed of Tigridia pavonia (Iridaceae) is anatropous, bitegmic, and crassinucellate. During development, the exotegmen is crushed and the endotegmen persists with tannins in the lumens and in the walls, which also react positively for lignin. The exotesta contains tannins and its outer walls are convex, thickened, and cuticularized. The mesotesta has multiple layers, accumulates abundant lipids, and forms a bulge in the chalaza. The cell walls of the endotesta collapse and accumulate tannins. In the chalaza, a hypostasal cushion contains tannins in the lumens and in the walls, which also react positively for lignin. At the micropylar end of the seed there is an operculum which consists of: a) a slightly crushed exotegmen, b) an endotegmen with cuticular thickenings that are concentric with respect to the micropyle, c) hemispherical deposists of cutin on the anticlinal walls of the endotegmen, and c) a thin layer of endosperm that covers the radicle. During its cellular stage of development, the endosperm has conspicuous transfer walls at the chalazal end next to the nucella. The embryo is small and has a conical cotyledon.

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