scholarly journals ASPECTOS CULTURAIS, MORFOLÓGICOS E MORFOMÉTRICOS DE Sordaria fimicola INCIDENTE EM FOLHAS DE CAPIM-MASSAMBARÁ (Sorghum arundinaceum)

2019 ◽  
Vol 6 (2) ◽  
pp. 34-44
Author(s):  
Andressa De Souza Almeida ◽  
Marcos Antônio Garcia Caetano da Costa ◽  
Lucinete Martins Barbosa Estrela ◽  
Milton Luiz Da Paz Lima
Keyword(s):  
Sordaria Fimicola

O capim-massambará (Sorghum arundinaceum) pode servir de fonte de inóculo de agentes de biocontrole como Sordaria spp. O objetivo deste trabalho foi avaliar o crescimento in vitro, a patogenicidade, caracterizar e identificar um isolado de Sordaria sp. incidente em capim-massambará. Amostras de folhas apresentando sintomas foram submetidas a isolamento em meio de cultura. A partir deste foram aplicados os seguintes testes: a) teste fisiológico – análise do crescimento micelial em meio de cultura. b) teste biológico – discos de micélio e solução de ascósporos foram inoculados em folhas; e c) identificação – caracterização morfológica das estruturas reprodutivas. O maior crescimento micelial foi observado nos meios BDA e ST. O isolado em condições artificiais não reproduziu os sintomas iniciais. O isolado apresentou peritécio gregário, semi-imerso em meio de cultura, sub-globoso, com organização celular reticulada, de dimensões de 1946,3-(1351,0)-507,9 × 1131,4-(828,2)-415,17 µm, com ostíolo de 413,85-(257,8)-123,8 µm; asca cilíndrica à clavada, unitunicada, de 195,0-(167,8)-135,6 × 21,8-(16,8)-9,1 µm; ascósporos apresentaram 29,7-(22,6)-13,7 × 14,9-(10,9)-1,6 µm. Com base nas características morfológicas e morfométricas, o isolado foi identificado como sendo S. fimicola.

scholarly journals Genetic Diversity Analysis and In Silico Investigation of Post-Translational Modifications of Carboxypeptidase A1 (CpA1) in Sordaria fimicola

2021 ◽  
Vol 25 (02) ◽  
pp. 475-482
Author(s):  
Uzma Naureen
Keyword(s):  
Genetic Diversity ◽  
Posttranslational Modifications ◽  
Nuclear Export ◽  
Serine Phosphorylation ◽  
Phosphorylation Sites ◽  
Multiple Sequence ◽  
Post Translational Modifications ◽  
Peptide Cleavage ◽  
Sordaria Fimicola

Post-translational modifications (PTMs) regulate different complex mechanisms of cell and affect cell growth, stress, evolution of living organisms and adaptations due to environment. The purpose of the present research is to investigate the genetic diversity and PTMs of protease (Carboxypeptidase A1) n Sordaria fimicola. They perform a variety of functions ranging from housekeeping: e.g., protein maturation, signal peptide cleavage, signal transduction, intracellular protein turnover, immune response, apoptosis, and reproduction. S. fimicola is a microscopic filamentous fungus, has been preferably used in this study because of its easy growing pattern on Potato Dextrose Agar (PDA) and a short life cycle of 7 to 12 days. The genomic DNA of six of the strains S. fimicola was used to amplify the carboxypeptidases A1 gene (CpA1), the product size was 940 bp. The multiple sequence alignment of the nucleotide sequences of six strains of S. fimicola with Neurospora crassa (as a reference strain) was studied. The numbers of polymorphic sites in six strains of S. fimicola with respect to N. crassa were six. Posttranslational modifications were depicted by using bioinformatics tools i.e., YinOYang1.2, NetPhos 3.1 and NetNES 1.1 Server to calculate O-glycosylation, phosphorylation sites, and nuclear export signals respectively. The study has predicted 19 phosphorylation sites on serine residues for protease Carboxypeptidase A1 in S1 strains of S. fimicola while 15 phosphorylation sites on serine in N7 strain and 17 serine phosphorylation modifications were predicted in N. Crassa. The results of this research will be helpful for further in vitro investigations of this industrially important enzyme under study. © 2021 Friends Science Publishers

The relative ability of fungi from Sphagnum fuscum to decompose selected carbon substrates

2002 ◽  
Vol 48 (3) ◽  
pp. 204-211 ◽  
Author(s):  
Markus N Thormann ◽  
Randolph S Currah ◽  
Suzanne E Bayley
Keyword(s):  
Tannic Acid ◽  
Wood Chips ◽  
Polyphenol Oxidases ◽  
Carbon Decomposition ◽  
Spruce Wood ◽  
Mass Losses ◽  
Sphagnum Fuscum ◽  
Carbon Substrates ◽  
Sordaria Fimicola

Nine species from a suite of 55 microfungi isolated from living and decomposing Sphagnum fuscum were selected for studies of in vitro decomposition of tannic acid, cellulose, and starch. In vitro decomposition of S. fuscum plants and spruce wood chips was also examined. Oidiodendron maius and Oidiodendron scytaloides degraded tannic acid, giving a positive reaction for polyphenol oxidases. Most taxa degraded cellulose and starch via the synthesis of cellulases and amylase, respectively. Mass losses of spruce wood chips generally exceeded those of S. fuscum. A basidiomycete, similar to Bjerkandera adusta, caused the greatest mass losses in spruce wood chips (10.2%), while O. scytaloides caused the smallest mass losses (3.4%) after 8 weeks. For S. fuscum, Sordaria fimicola caused the greatest (5.1%) and Mucor hiemalis the smallest (0.1%) mass losses after 8 weeks. Filamentous microfungi have considerable potential to decompose a variety of carbon substrates of bryophilous residues in peatlands.Key words: microfungi, Sphagnum fuscum, peatlands, carbon, decomposition.

Ultrastructural Investigations of the Contractile Filaments of Amoebae

1974 ◽  
Vol 32 ◽  
pp. 188-189
Author(s):  
P.L. Moore
Keyword(s):  
Cytoplasmic Streaming ◽  
Three Dimensional ◽  
Freeze Fracture ◽  
Amoeboid Movement ◽  
Different Types ◽  
Chemical Conditions ◽  
Complete Interpretation

Previous freeze fracture results on the intact giant, amoeba Chaos carolinensis indicated the presence of a fibrillar arrangement of filaments within the cytoplasm. A complete interpretation of the three dimensional ultrastructure of these structures, and their possible role in amoeboid movement was not possible, since comparable results could not be obtained with conventional fixation of intact amoebae. Progress in interpreting the freeze fracture images of amoebae required a more thorough understanding of the different types of filaments present in amoebae, and of the ways in which they could be organized while remaining functional.The recent development of a calcium sensitive, demembranated, amoeboid model of Chaos carolinensis has made it possible to achieve a better understanding of such functional arrangements of amoeboid filaments. In these models the motility of demembranated cytoplasm can be controlled in vitro, and the chemical conditions necessary for contractility, and cytoplasmic streaming can be investigated. It is clear from these studies that “fibrils” exist in amoeboid models, and that they are capable of contracting along their length under conditions similar to those which cause contraction in vertebrate muscles.

In Vitro Induction of Crystals of MT Protein by Vinblastine-Colcemid in Mouse Spermatids

1974 ◽  
Vol 32 ◽  
pp. 132-133
Author(s):  
John J. Wolosewick ◽  
John H. D. Bryan
Keyword(s):  
Endoplasmic Reticulum ◽  
Smooth Endoplasmic Reticulum ◽  
Nuclear Ring ◽  
Rough Er ◽  
Distal Direction ◽  
In Vitro Induction

Early in spermiogenesis the manchette is rapidly assembled in a distal direction from the nuclear-ring-densities. The association of vesicles of smooth endoplasmic reticulum (SER) and the manchette microtubules (MTS) has been reported. In the mouse, osmophilic densities at the distal ends of the manchette are the organizing centers (MTOCS), and are associated with the SER. Rapid MT assembly and the lack of rough ER suggests that there is an existing pool of MT protein. Colcemid potentiates the reaction of vinblastine with tubulin and was used in this investigation to detect this protein.

Induction and Differentiation of Dental Epithelium in Vivo and in Vitro

1982 ◽  
Vol 40 ◽  
pp. 142-145
Author(s):  
E. J. Kollar
Keyword(s):  
Connective Tissue ◽  
Oral Mucosa ◽  
Basal Lamina ◽  
Functional Derivatives ◽  
Specific Source ◽  
Dental Epithelium ◽  
Connective Tissue Stroma

The differentiation and maintenance of many specialized epithelial structures are dependent on the underlying connective tissue stroma and on an intact basal lamina. These requirements are especially stringent in the development and maintenance of the skin and oral mucosa. The keratinization patterns of thin or thick cornified layers as well as the appearance of specialized functional derivatives such as hair and teeth can be correlated with the specific source of stroma which supports these differentiated expressions.

Immunoenzymatic demonstration of the simultaneous presence of transferrin, hemopexin and albumin in a same hepatocyte and their ultrastructural localization

1978 ◽  
Vol 36 (2) ◽  
pp. 88-89
Author(s):  
M. Kraemer ◽  
J. Foucrier ◽  
J. Vassy ◽  
M.T. Chalumeau
Keyword(s):  
Plasma Proteins ◽  
Rat Hepatocytes ◽  
Ultrastructural Localization ◽  
Carrier Proteins ◽  
Normal Cells ◽  
Adult Rat ◽  
Adult Rat Hepatocytes ◽  
Monospecific Antisera ◽  
Different Levels

Some authors using immunofluorescent techniques had already suggested that some hepatocytes are able to synthetize several plasma proteins. In vitro studies on normal cells or on cells issued of murine hepatomas raise the same conclusion. These works could be indications of an hepatocyte functionnal non-specialization, meanwhile the authors never give direct topographic proofs suitable with this hypothesis.The use of immunoenzymatic techniques after obtention of monospecific antisera had seemed to us useful to bring forward a better knowledge of this problem. We have studied three carrier proteins (transferrin = Tf, hemopexin = Hx, albumin = Alb) operating at different levels in iron metabolism by demonstrating and localizing the adult rat hepatocytes involved in their synthesis.Immunological, histological and ultrastructural methods have been described in a previous work.

Sem Studies of Co-Cr-Mo Surgical Implant Alloy Corrosion Behavior

1982 ◽  
Vol 40 ◽  
pp. 520-521
Author(s):  
Ann Chidester Van Orden ◽  
John L. Chidester ◽  
Anna C. Fraker ◽  
Pei Sung
Keyword(s):  
Electron Microscopy ◽  
Corrosion Behavior ◽  
Anodic Polarization ◽  
Saline Solution ◽  
Saturated Calomel Electrode ◽  
Physiological Saline ◽  
X Ray ◽  
Physiological Saline Solution ◽  
Scanning Electron

The influence of small variations in the composition on the corrosion behavior of Co-Cr-Mo alloys has been studied using scanning electron microscopy (SEM), energy dispersive x-ray analysis (EDX), and electrochemical measurements. SEM and EDX data were correlated with data from in vitro corrosion measurements involving repassivation and also potentiostatic anodic polarization measurements. Specimens studied included the four alloys shown in Table 1. Corrosion tests were conducted in Hanks' physiological saline solution which has a pH of 7.4 and was held at a temperature of 37°C. Specimens were mechanically polished to a surface finish with 0.05 µm A1203, then exposed to the solution and anodically polarized at a rate of 0.006 v/min. All voltages were measured vs. the saturated calomel electrode (s.c.e.).. Specimens had breakdown potentials near 0.47V vs. s.c.e.

Ultrastructural Correlations between Clonal Human Tumor Colonies and in Vivo Neoplasms

1982 ◽  
Vol 40 ◽  
pp. 210-211
Author(s):  
M.J. Murphy ◽  
R.R. Price ◽  
J.C. Sloman
Keyword(s):  
Cultured Cells ◽  
Human Tumor ◽  
Cell Type ◽  
Tumor Mass ◽  
Initial Cell ◽  
Cloning Assay ◽  
Human Tumor Cloning ◽  
The Relationship

The in vitro human tumor cloning assay originally described by Salmon and Hamburger has been applied recently to the investigation of differential anti-tumor drug sensitivities over a broad range of human neoplasms. A major problem in the acceptance of this technique has been the question of the relationship between the cultured cells and the original patient tumor, i.e., whether the colonies that develop derive from the neoplasm or from some other cell type within the initial cell population. A study of the ultrastructural morphology of the cultured cells vs. patient tumor has therefore been undertaken to resolve this question. Direct correlation was assured by division of a common tumor mass at surgical resection, one biopsy being fixed for TEM studies, the second being rapidly transported to the laboratory for culture.

Maytansine-Induced Mitotic Arrest in Human Lymphoblasts

1977 ◽  
Vol 35 ◽  
pp. 460-461
Author(s):  
Tai-Te Chao ◽  
John Sullivan ◽  
Awtar Krishan
Keyword(s):  
Electron Microscopy ◽  
Cell Cycle ◽  
Transmission Electron Microscopy ◽  
Tubulin Polymerization ◽  
Vinca Alkaloids ◽  
Antimitotic Activity ◽  
Transmission Electron ◽  
Flow Microfluorometry ◽  
Brain Tubulin

Maytansine, a novel ansa macrolide (1), has potent anti-tumor and antimitotic activity (2, 3). It blocks cell cycle traverse in mitosis with resultant accumulation of metaphase cells (4). Inhibition of brain tubulin polymerization in vitro by maytansine has also been reported (3). The C-mitotic effect of this drug is similar to that of the well known Vinca- alkaloids, vinblastine and vincristine. This study was carried out to examine the effects of maytansine on the cell cycle traverse and the fine struc- I ture of human lymphoblasts.Log-phase cultures of CCRF-CEM human lymphoblasts were exposed to maytansine concentrations from 10-6 M to 10-10 M for 18 hrs. Aliquots of cells were removed for cell cycle analysis by flow microfluorometry (FMF) (5) and also processed for transmission electron microscopy (TEM). FMF analysis of cells treated with 10-8 M maytansine showed a reduction in the number of G1 cells and a corresponding build-up of cells with G2/M DNA content.

Cytochemical Evidence for Presynatic β-Adrenergic Regulation of Secretion in the Developing Rat Submandibular Gland

1977 ◽  
Vol 35 ◽  
pp. 430-431
Author(s):  
L.S. Cutler
Keyword(s):  
Cyclic Amp ◽  
Adenylate Cyclase ◽  
Submandibular Gland ◽  
Neonatal Rat ◽  
Cyclase Activity ◽  
Adenylate Cyclase Activity ◽  
Parotid Glands ◽  
Adrenergic Agonist ◽  
Rat Submandibular Gland

Many studies previously have shown that the B-adrenergic agonist isoproterenol and the a-adrenergic agonist norepinephrine will stimulate secretion by the adult rat submandibular (SMG) and parotid glands. Recent data from several laboratories indicates that adrenergic agonists bind to specific receptors on the secretory cell surface and stimulate membrane associated adenylate cyclase activity which generates cyclic AMP. The production of cyclic AMP apparently initiates a cascade of events which culminates in exocytosis. During recent studies in our laboratory it was observed that the adenylate cyclase activity in plasma membrane fractions derived from the prenatal and early neonatal rat submandibular gland was retractile to stimulation by isoproterenol but was stimulated by norepinephrine. In addition, in vitro secretion studies indicated that these prenatal and neonatal glands would not secrete peroxidase in response to isoproterenol but would secrete in response to norepinephrine. In contrast to these in vitro observations, it has been shown that the injection of isoproterenol into the living newborn rat results in secretion of peroxidase by the SMG (1).

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