scholarly journals Cultivo in vitro de Epidendrum nocturnum (Orchidaceae) ocorrente no Cerrado da região Centro-Oeste

Rodriguésia ◽  
2016 ◽  
Vol 67 (4) ◽  
pp. 1083-1091 ◽  
Author(s):  
Carlos de Sousa Silva ◽  
Leila Garcês de Araújo ◽  
Kellen Cristhina Inácio Sousa ◽  
Jacqueline Campos Borba de Carvalho ◽  
Letícia de Almeida Gonçalves ◽  
...  
Keyword(s):  
Waitea Circinata

Resumo As orquídeas podem ser propagadas in vitro em meios de cultivo assépticos ou em simbiose com fungos micorrízicos. Epidendrum nocturnum ocorre em áreas de Cerrado e neste estudo objetivou-se a visualização de fungos micorrízicos em suas raízes bem como o cultivo assimbiótico de suas plântulas em diferentes meios e a micorrização in vitro. No desenvolvimento assimbiótico testou-se três meios de cultura em um ensaio e, em outro ensaio, foram testadas formulações alternativas do meio Knudson C modificado, com a adição de polpa de frutas. Fungos micorrízicos de orquídeas foram usados na micorrização in vitro. Pelotons foram visualizados nas raízes de E. nocturnum. O meio Knudson C modificado diferiu estatisticamente dos demais, nas duas intensidades luminosas, no primeiro ensaio. No segundo ensaio, após sete meses, os meios com formulação alternativa não diferiram estatisticamente entre si. Na micorrização in vitro as plântulas com o isolado fúngico En07 (Waitea circinata) apresentaram maior vigor visual em relação aos demais tratamentos, mas não houve diferença estatística com o controle. Os meios com formulação alternativa e o Knudson C modificado podem ser utilizados no desenvolvimento in vitro de E. nocturnum e o isolado En07 pode ser usado na micorrização visando estratégias de conservação desta orquídea.

scholarly journals Efficiency of a new Waitea circinata extract against rice pathogens

2021 ◽  
Vol 51 ◽  
Author(s):  
Jacqueline Campos Borba de Carvalho ◽  
Amanda Abdallah Chaibub ◽  
Kellen Cristhina Inácio Sousa ◽  
Denise Candini de Brito ◽  
Marta Cristina Corsi de Filippi ◽  
...  
Keyword(s):  
Rice Blast ◽  
Mycorrhizal Fungus ◽  
Conidial Germination ◽  
Appressorium Formation ◽  
Vitro Assay ◽  
Rice Pathogens ◽  
Waitea Circinata ◽  
Mycelial Mass

ABSTRACT Waitea circinata (Warcup & Talbot) is an orchid antagonist mycorrhizal fungus with biocontrol potential against rice pathogens. This study aimed to optimize the extraction method, obtain a new extract and evaluate its efficiency against rice pathogens in vitro and in vivo, as well as to compare it with other extraction methods and W. circinata. The extracts were obtained and screened for in vitro growth inhibition against the pathogens Cochliobolus miyabeanus, Monographella albescens and Sarocladium oryzae, using the following extracts: mycelial, crude, lyophilized and mycelial mass. An additional in vitro assay was performed with the principal rice pathogen (Magnaporthe oryzae), in order to evaluate the conidial germination and appressorium formation. Based on this evaluation, the lyophilized and mycelial mass extracts were tested in vivo against rice blast (M. oryzae) and compared to the W. circinata mycelial suspension, in different application forms (simultaneous and previous). The mycelial mass extract inhibited all the pathogens, and the crude and lyophilized extracts inhibited C. miyabeanus and M. albescens, respectively. The mycelial mass extract inhibited the M. oryzae conidial germination and appressorium formation by 80 %, and the simultaneous and previous applications suppressed the rice blast by 94 %. These results indicate that the new extract can be used to control rice pathogens.

scholarly journals In Vitro Fungicide Sensitivity of Rhizoctonia and Waitea Isolates Collected from Turfgrasses

2014 ◽  
Vol 32 (3) ◽  
pp. 126-132 ◽  
Author(s):  
Bimal S. Amaradasa ◽  
Dilip Lakshman ◽  
David S. McCall ◽  
Brandon J. Horvath
Keyword(s):  
Radial Growth ◽  
Geographic Origin ◽  
Fungicide Sensitivity ◽  
Disease Symptoms ◽  
Anastomosis Groups ◽  
Inhibition Of Growth ◽  
Variable Sensitivity ◽  
Moderate Sensitivity ◽  
Waitea Circinata

Different Rhizoctonia species and anastomosis groups (AGs) have been reported to show variable sensitivity to commercial fungicides. Thirty-six isolates of Rhizoctonia collected from turfgrasses were tested in vitro for sensitivity to commercial formulations of iprodione, triticonazole, and pyraclostrobin. Tested isolates represented R. solani AG 1-IB and AG 2-2IIIB; W. circinata varieties zeae (Wcz) and circinata (Wcc); and binucleate Rhizoctonia-like fungi (BNR) from different locations in Virginia and Maryland. Each fungicide was added to PDA medium to obtain concentrations at 0, 0.1, 1, 10 and 100 mg a.i.·L−1 (0.00001, 0.0001, 0.001 and 0.01 oz a.i.·gal−1). A mycelium plug from each isolate was grown on these plates. The fungicide concentration needed for 50% inhibition of radial growth (EC50) was determined for each isolate by fungicide combination. Waitea circinata isolates were moderately sensitive (EC50 = 1 to 10 mg a.i.·L−1) (0.0001 to 0.001 oz a.i.·gal−1) to iprodione while isolates of R. solani and BNR were extremely sensitive (EC50 < 1 mg a.i.·L−1). Isolates of AG 2-2IIIB exhibited less sensitivity to triticonazole (mean EC50 = 1.26 mg a.i.·L−1) than AG 1-IB and W. circinata (mean EC50 = 0.2, and 0.06 mg a.i.·L−1, respectively). BNR isolates varied in inhibition of growth by triticonazole, exhibiting extreme to moderate sensitivity. Isolates of W. circinata were moderately sensitive to pyraclostrobin while most cultures of R. solani and BNR were extremely sensitive. Geographic origin of isolates had no influence on the level of fungicide sensitivity. This study demonstrates the importance of accurately identifying the Rhizoctonia pathogen causing disease symptoms on a turfgrass for choosing an effective fungicide.

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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