ISSN 2756-3707
Research Article
International Journal of Histology and Cytology ISSN 2447-9535 Vol. 3 (9), pp. 283-286, September, 2016. © International Scholars Journals
Full Length Research Paper
GARCINIA KOLA extract reduced lipopolysaccharide activation of macrophages using U937 cells as a model
Tebekeme Okoko1* and Ibiba F. Oruambo2
1Biochemistry Division, Department of Chemical Sciences, Niger Delta University, PMB 71, Yenagoa, Bayelsa State, Nigeria.
2Department of Chemistry, River State University of Science and Technology, Port Harcourt, Rivers State, Nigeria.
*Corresponding author. E-mail: [email protected]. Tel. +2348051069342.
Accepted 03 January, 2016
Abstract
The effect of GARCINIA KOLA heckel seed extract on the promonocytic cell line U937 activated by lipopolysaccharide (LPS) was investigated. 200 µl of U937 cells maintained in culture at 5 x 105 cells per ml was delivered into wells of a culture plate according to groups. Cells were pre-treated with 20 µl of 100 ng/ml phorbol myristate acetate (PMA) for 24, 48, or 72 h in order to transform them to the macrophage form. Following the PMA treatment, some cells were incubated with 100 µg/ml LPS (group C), while others (group D) were treated with 100 µg/ml LPS and 100 µl of 100 µg/ml of the G. KOLA methanolic extract. Other cells (groups A, and B) were incubated with neither LPS nor extract. 24 h later, the supernatants were analysed for the production of TNF-α and IL6 as indices for the activation of macrophages. The results show that the G. KOLA extract reduced the tendency of LPS to activate the cells. However, highest activation of LPS was observed when the cells were incubated with PMA for 48 h prior to the addition of LPS. This suggests that stimulation of U937 cells with PMA is necessary for the production of cytokines and that G. kola possesses considerable immunomodulatory activity.
Key words: Garcinia kola, lipopolysaccharide, phorbol myristate acetate, macrophage, cytokines.
Ibiba F. Oruambo, Tebekeme Okoko*
Research Article
A study of the optimum culture conditions and factors involved in maximum production of glucoamylase
International Journal of Histology and Cytology ISSN 2447-9535 Vol. 3 (1), pp. 235-240, January, 2016. © International Scholars Journals
Full Length Research Paper
A study of the optimum culture conditions and factors involved in maximum production of glucoamylase
Lagzouli Mohamed1*, Mennane Zakaria 1, Aitounejjar Ali2, Wafae Senhaji3, Ouhssine Mohamed1, Elyachioui Mohamed1, Berny EL Hassan1 and Jadal Mohamed
1Laboratory of Microbial Biotechnology, University IBN TOFAIL, Department of Sciences, BP 133, 14000 Kenitra-Morocco.
2National Institute of Agronomic Researches, INRA, BP: 589 Settat 26000, Morocco.
3Laboratoire de Recherche et d'Analyses Médicales de la Gendarmerie Royale, avenue Ibn Sina-Agdal-Rabat, B.P 8087, 10000, Morocco.
*Corresponding author. E-mail: [email protected].
Accepted 16 March, 2007
Abstract
Candida famata was isolated from traditional Moroccan sourdough. It exhibited high glucoamylase and biomass production. Starch induces high glucoamylase production C. famata with maximum glucoamylase activity at 5 g/L. Glucose stimulates good production in biomass but strongly inhibits glucoamylase production. Among the sources of nitrogen tested, yeast extract and the (NH4)2HPO4 gave maximum glucoamylase and biomass after 72 h of incubation in liquid medium at 30°C, pH 5 and 105 rpm.
Key words: Glucoamylase, yeast, optimization, biotechnology, Candida famata.
Mennane Zakaria, Aitounejjar Ali, Elyachioui Mohamed, Wafae Senhaji, Lagzouli Mohamed*, Ouhssine Mohamed, Berny EL Hassan and Jadal Mohamed
Short Communication
Saccharification of banana agro-waste by cellulolytic enzymes
International Journal of Histology and Cytology ISSN 2447-9535 Vol. 2 (7), pp. 225-228, July, 2015. © International Scholars Journals
Short Communication
Saccharification of banana agro-waste by cellulolytic enzymes
M.M.V. Baig1*, M.L.B. Baig1, M.I.A. Baig2 and Majeda Yasmeen1
1Botany Research Laboratory & Plant Disease Clinic, Science College, Nanded 431605 India.
2Department of Agronomy, College of Agriculture, Marathwada Agricultural University, Parbhani 431402, India.
*Correspondence author. E-mail: [email protected].
Accepted 22 March, 2014
Abstract
Banana is major cash crop of this region generating vast agricultural waste after harvest. The agro-waste including dried leaves and psuedostem after harvest was used as substrate for the release of sugars. Saccharification of banana agro waste by cellulases of Trichoderma lignorum was investigated. The steam treated agro-waste yielded 1.34 mg/ml of reducing sugars after 24 hr. The size of substrate affected saccharification where the smaller size (<120 µ) yield more sugars. Maximum sugars were released at pH 6.0 whereas 40°C was the optimum temperature. Thus, under these conditions the agro waste left behind for natural degradation can be utilized affectively to yield fermentable sugars which can be converted into other substances like alcohol.
Key words: Banana agrowaste, Trichoderma lignorum, cellulases, saccharification
M.I.A. Baig and Majeda Yasmeen, M.L.B. Baig, M.M.V. Baig*
Review
Thin Cell Layer technology and their application in ornamental plant micropropagation
International Journal of Histology and Cytology ISSN 2447-9535 Vol. 2 (6), pp. 180-189, June, 2015. © International Scholars Journals
Review
Thin Cell Layer technology and their application in ornamental plant micropropagation
Esaki Toshiki
Department of Agronomy, Faculty of Agriculture, University, Kinjo University. E-mail: esaki.toshili@ kinjo.ac.jp
Accepted 02 August, 2014
Abstract
Thin cell layer (TCL) technology originated almost 30 years ago with the controlled development of flowers, roots, shoots and somatic embryos on tobacco pedicel longitudinal TCLs. Since then TCLs have been successfully used in the micropropagation of many ornamental plant species whose previous in vitro regeneration was not successful using conventional methods. This review examines the fundamentals behind TCLs, and their application in ornamental plant micropropagation and transformation.
Key words: Chrysanthemum, lily, somatic embryogenesis, thin cell layer, tobacco, transformation.
Esaki Toshiki
Review
International Journal of Histology and Cytology ISSN 2447-9535 Vol. 2 (6), pp. 208-212, June, 2015. © International Scholars Journals
Review
Identification of premeiotic and meiotic mutants in Arabidopsis thaliana through innovative approaches
F. Consiglio1, C. Conicella1 , L. Monti1 and D. Carputo2*
1CNR-IGV, Institute of Plant Genetics, Research Division Portici, Via Università 133, 80055 Portici, Italy
2DISSPA, Dept. of Soil, Plant and Environmental Sciences, University of Naples "Federico II", Via Università 100, 80055 Portici, Italy
*Corresponding author. Tel: ++39-081-2539225. Fax: ++39-081-7753579. E-mail: [email protected].
Accepted 09 January, 2015
Abstract
Meiosis is a fascinating and complex phenomenon and, despite its central role in sexual plant reproduction, little is known on the molecular mechanisms involved in this process. We review the progress made in recent years using Arabidopsis thaliana mutants for isolating meiotic genes. In particular, emphasis is given on the description of mutants affecting either the regular commitment to meiosis, or the mechanisms of synapsis, recombination, and cytokinesis. We believe that the isolation of genes affecting some crucial meiotic events may represent the first step towards the practical use of meiotic genes in plant breeding. The introduction of deviations in the meiotic pathway into sexual crops will have important implications for the exploitation of apomixis and sexual polyploidization.
Key words: Arabidopsis, meiosis, mutants, fertility.
F. Consiglio, L. Monti and D. Carputo*, C. Conicella
Research Article
A study of the introduction of β-glucosidase genes into Saccharomyces cerevisiae
International Journal of Histology and Cytology ISSN 2447-9535 Vol. 2 (6), pp. 213-216, June, 2015. © International Scholars Journals
Full Length Research Paper
A study of the introduction of β-glucosidase genes into Saccharomyces cerevisiae
S. Parvez*, Z. Mukhtar, F. Rashid, M.I. Rajoka
National Institute for Biotechnology & Genetic Engineering, P.O. Box 577, Jhang Road, Faisalabad, Pakistan.
*Corresponding author. E-mail: [email protected].
Accepted 06 February, 2015
Abstract
A β-glucosidase genomic DNA from Cellulomonas biazotea NIAB 442 was isolated and coated onto tungsten microprojectiles for direct transformation of the gene into Saccharomyces cerevisiae. Transformation of β-glucosidase into S. cerevisae conferred the ability to hydrolyse esculin and cellobiose, indicating that the gene is expressed in the bombarded yeast.
Key words: Biolistic transformation, β-glucosidase, Cellulomonas biazotea, Saccharomyces cerevisiae.
F. Rashid, M.I. Rajoka, Z. Mukhtar, S. Parvez*