Aerobic and Anaerobic Bacterial and Fungal Degradation of Pyrene: Mechanism Pathway Including Biochemical Reaction and Catabolic Genes
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The Harmful Effects of Food Preservatives on Human Health Shazia Khanum Mirza1, U.K
Journal of Medicinal Chemistry and Drug Discovery ISSN: 2347-9027 International peer reviewed Journal Special Issue Analytical Chemistry Teacher and Researchers Association National Convention/Seminar Issue 02, Vol. 02, pp. 610-616, 8 January 2017 Available online at www.jmcdd.org To Study The Harmful Effects Of Food Preservatives On Human Health Shazia Khanum Mirza1, U.K. Asema2 And Sayyad Sultan Kasim3. 1 -Research student , Dept of chemistry, Maulana Azad PG & Research centre, Aurangabad. 2-3 -Assist prof. Dept of chemistry,Maulana Azad college Arts sci & com.Aurangabad. ABSTRACT Food chemistry is the study of chemical processes and interactions of all biological and non- biological components. Food additives are chemicals added to foods to keep them fresh or to enhance their color, flavor or texture. They may include food colorings, flavor enhancers or a range of preservatives .The chemical added to a particular food for a particular reason during processing or storage which could affect the characteristics of the food, or become part of the food Preservatives are additives that inhibit the growth of bacteria, yeasts, and molds in foods. Additives and preservatives are used to maintain product consistency and quality, improve or maintain nutritional value, maintain palatability and wholesomeness, provide leavening(yeast), control pH, enhance flavour, or provide colour Some additives have been used for centuries; for example, preserving food by pickling (with vinegar), salting, as with bacon, preserving sweets or using sulfur dioxide as in some wines. Some preservatives are known to be harmful to the human body. Some are classified as carcinogens or cancer causing agents. Keywords : Food , Food additives, colour, flavour , texture, preservatives. -
The Effect Off Ethylenediamine Tetraacetic Acid 4 the Antimicrobial Properties of Benzoic
University of Nigeria Virtual Library Serial No ISSN: 1118-1028 Author 1 MBAH, Chika J. Author 2 Author 3 Title The Effect of Ethylenediamine Tetraacetic Acid on the Antimicrobial Properties of Benzoic Acid and Cetrimide Keywords Description Pharmaceutical Chemistry Category Pharmaceutical Sciences Publisher Publication Date 1999 Signature * - ' 8 - . 1 I r/ Journal of I PHARMACEUTICAL 1 RESEARCH AND i .DEVELOPMENT Journal of Pharmaceutical Research and Development 4: 1 (1 999) 1 -8 - 1 : The Effect offEthylenediamine Tetraacetic Acid 4 the Antimicrobial Properties of Benzoic ) Acid and Cetrimide C. 0. Esirnonel* M. U. ~dikwu';D.B. Uzuegbu' and 0. P. Udeo 4 'Division of Pharmaceutical Microbiology Department of Pharmz Faculty of Phyackutical Sciences University of Nigeria, Ws I 'Department of ~harmacolo~~and Toxicology, Faculty of Pharmaceut ' . University of Nigeria,fisukka. i I I : I. The effect of ethylenediamine tetraacetic acid (EDTA) on the in-vp antimicrobial activities of cetrimide and benzoic acid was evaluated by the checkerboardland killing curve method. The effect sf EDTA aid benzoic acid was evaluated against an isolate of Pseirdonionas aeruginosa (Ps. 021) which is highly resistant to either of the drugs alone. The effect of EDTA and cetrimide was evaluated against isolates of Aspergillus niger and Candidn albicarls resistant to either of the agents. The results show that in the'presence of EDTA, the bacteriostatic and bactericidal effects of benzoic acid and cetrimide against the test microorgan,isms were greatly enhanced. Checkerboard analy& revealed striking synergy (FIC indices > 1 and negative values of activity indices) between almost all the ratios of EDTA and the antimicrobial agents against the various test microorganisms. -
Benzoic Acid
SAFETY DATA SHEET Creation Date 01-May-2012 Revision Date 23-Jan-2015 Revision Number 2 1. Identification Product Name Benzoic acid Cat No. : A63-500; A65-500; A68-30 Synonyms Benzenecarboxylic acid; Benzenemethanoic acid; Phenylcarboxylic acid; Phenylformic acid; Benzeneformic acid; Carboxybenzene Recommended Use Laboratory chemicals. Uses advised against No Information available Details of the supplier of the safety data sheet Company Emergency Telephone Number Fisher Scientific CHEMTRECÒ, Inside the USA: 800-424-9300 One Reagent Lane CHEMTRECÒ, Outside the USA: 001-703-527-3887 Fair Lawn, NJ 07410 Tel: (201) 796-7100 2. Hazard(s) identification Classification This chemical is considered hazardous by the 2012 OSHA Hazard Communication Standard (29 CFR 1910.1200) Skin Corrosion/irritation Category 2 Serious Eye Damage/Eye Irritation Category 1 Specific target organ toxicity - (repeated exposure) Category 1 Target Organs - Lungs. Label Elements Signal Word Danger Hazard Statements Causes skin irritation Causes serious eye damage Causes damage to organs through prolonged or repeated exposure ______________________________________________________________________________________________ Page 1 / 7 Benzoic acid Revision Date 23-Jan-2015 ______________________________________________________________________________________________ Precautionary Statements Prevention Wash face, hands and any exposed skin thoroughly after handling Wear protective gloves/protective clothing/eye protection/face protection Do not breathe dust/fume/gas/mist/vapors/spray Do not eat, drink or smoke when using this product Response Get medical attention/advice if you feel unwell Skin IF ON SKIN: Wash with plenty of soap and water If skin irritation occurs: Get medical advice/attention Take off contaminated clothing and wash before reuse Eyes IF IN EYES: Rinse cautiously with water for several minutes. -
Pseudomonas Chloritidismutans Sp. Nov., a Non- Denitrifying, Chlorate-Reducing Bacterium
International Journal of Systematic and Evolutionary Microbiology (2002), 52, 2183–2190 DOI: 10.1099/ijs.0.02102-0 Pseudomonas chloritidismutans sp. nov., a non- denitrifying, chlorate-reducing bacterium Laboratory of Microbiology, A. F. W. M. Wolterink, A. B. Jonker, S. W. M. Kengen and A. J. M. Stams Wageningen University, H. van Suchtelenweg 4, 6703 CT Wageningen, Author for correspondence: The Netherlands A. F. W. M. Wolterink. Tel: j31 317 484099. Fax: j31 317 483829. e-mail: Arthur.Wolterink!algemeen.micr.wag-ur.nl A Gram-negative, facultatively anaerobic, rod-shaped, dissimilatory chlorate- reducing bacterium, strain AW-1T, was isolated from biomass of an anaerobic chlorate-reducing bioreactor. Phylogenetic analysis of the 16S rDNA sequence showed 100% sequence similarity to Pseudomonas stutzeri DSM 50227 and 986% sequence similarity to the type strain of P. stutzeri (DSM 5190T). The species P. stutzeri possesses a high degree of genotypic and phenotypic heterogeneity. Therefore, eight genomic groups, termed genomovars, have been proposed based upon ∆Tm values, which were used to evaluate the quality of the pairing within heteroduplexes formed by DNA–DNA hybridization. In this study, DNA–DNA hybridization between strain AW-1T and P. stutzeri strains DSM 50227 and DSM 5190T revealed respectively 805 and 565% similarity. DNA–DNA hybridization between P. stutzeri strains DSM 50227 and DSM 5190T revealed 484% similarity. DNA–DNA hybridization indicated that strain AW-1T is not related at the species level to the type strain of P. stutzeri. However, strain AW-1T and P. stutzeri DSM 50227 are related at the species level. The physiological and biochemical properties of strain AW-1T and the two P. -
Section 4. Guidance Document on Horizontal Gene Transfer Between Bacteria
306 - PART 2. DOCUMENTS ON MICRO-ORGANISMS Section 4. Guidance document on horizontal gene transfer between bacteria 1. Introduction Horizontal gene transfer (HGT) 1 refers to the stable transfer of genetic material from one organism to another without reproduction. The significance of horizontal gene transfer was first recognised when evidence was found for ‘infectious heredity’ of multiple antibiotic resistance to pathogens (Watanabe, 1963). The assumed importance of HGT has changed several times (Doolittle et al., 2003) but there is general agreement now that HGT is a major, if not the dominant, force in bacterial evolution. Massive gene exchanges in completely sequenced genomes were discovered by deviant composition, anomalous phylogenetic distribution, great similarity of genes from distantly related species, and incongruent phylogenetic trees (Ochman et al., 2000; Koonin et al., 2001; Jain et al., 2002; Doolittle et al., 2003; Kurland et al., 2003; Philippe and Douady, 2003). There is also much evidence now for HGT by mobile genetic elements (MGEs) being an ongoing process that plays a primary role in the ecological adaptation of prokaryotes. Well documented is the example of the dissemination of antibiotic resistance genes by HGT that allowed bacterial populations to rapidly adapt to a strong selective pressure by agronomically and medically used antibiotics (Tschäpe, 1994; Witte, 1998; Mazel and Davies, 1999). MGEs shape bacterial genomes, promote intra-species variability and distribute genes between distantly related bacterial genera. Horizontal gene transfer (HGT) between bacteria is driven by three major processes: transformation (the uptake of free DNA), transduction (gene transfer mediated by bacteriophages) and conjugation (gene transfer by means of plasmids or conjugative and integrated elements). -
Microflex Gloves Chemical Compatibility Chart
1 1 1 2 2 3 1 CAUTION (LATEX): This product contains natural rubber 2 CAUTION (NITRILE: MEDICAL GRADE): Components used 3 CAUTION (NITRILE: NON-MEDICAL GRADE)): These latex (latex) which may cause allergic reactions. Safe use in making these gloves may cause allergic reactions in gloves are for non-medical use only. They may NOT be of this glove by or on latex sensitized individuals has not some users. Follow your institution’s policies for use. worn for barrier protection in medical or healthcare been established. applications. Please select other gloves for these applications. Components used in making these gloves may cause allergic reactions in some users. Follow your institution’s policies for use. For single use only. NeoPro® Chemicals NeoPro®EC Ethanol ■NBT Ethanolamine (99%) ■NBT Ether ■2 Ethidium bromide (1%) ■NBT Ethyl acetate ■1 Formaldehyde (37%) ■NBT Formamide ■NBT Gluteraldehyde (50%) ■NBT Test Method Description: The test method uses analytical Guanidine hydrochloride ■NBT equipment to determine the concentration of and the time at which (50% ■0 the challenge chemical permeates through the glove film. The Hydrochloric acid ) liquid challenge chemical is collected in a liquid miscible chemical Isopropanol ■NBT (collection media). Data is collected in three separate cells; each cell Methanol ■NBT is compared to a blank cell which uses the same collection media as both the challenge and Methyl ethyl ketone ■0 collection chemical. Methyl methacrylate (33%) ■0 Cautionary Information: These glove recommendations are offered as a guide and for reference Nitric acid (50%) ■NBT purposes only. The barrier properties of each glove type may be affected by differences in material Periodic acid (50%) ■NBT thickness, chemical concentration, temperature, and length of exposure to chemicals. -
Effect of Toluene on Pseudomonas Stutzeri ST-9 Morphology: Plasmolysis, Cell Size and 1
Canadian Journal of Microbiology Effect of toluene on Pseudomonas stutzeri ST -9 morphology: Plasmolysis, cell size and formation of outer membrane vesicles Journal: Canadian Journal of Microbiology Manuscript ID cjm-2016-0099.R1 Manuscript Type: Article Date Submitted by the Author: 18-Mar-2016 Complete List of Authors: Michael, Esti; Ariel University, Chemical Engineering Nitzan, YeshayahuDraft ; Bar-Ilan University Langzam, Yakov; Bar-Ilan University, The Mina & Everard Goodman Faculty of Life Sciences Luboshits, Galia ; Ariel University, Cahan, Rivka; Ariel University, Chemical Engineering Keyword: Pseudomonas, plasmolysis, toluene, outer membrane vesicles, morphology https://mc06.manuscriptcentral.com/cjm-pubs Page 1 of 27 Canadian Journal of Microbiology Effect of toluene on Pseudomonas stutzeri ST-9 morphology: Plasmolysis, cell size and 1 formation of outer membrane vesicles 2 3 Esti Michael 1,2 , Yeshayahu Nitzan 2, Yakov Langzam 2, Galia Luboshits 1 and Rivka Cahan 1* 4 1Department of Chemical Engineering, Ariel University, Ariel 40700, Israel 5 2The Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, 6 Ramat-Gan 52900, Israel 7 *Corresponding author 8 9 10 11 Draft 12 13 14 15 16 17 18 19 20 21 22 23 24 25 1 https://mc06.manuscriptcentral.com/cjm-pubs Canadian Journal of Microbiology Page 2 of 27 Abstract 1 Isolated toluene-degrading Pseudomonas stutzeri ST-9 bacteria were grown in a minimal 2 medium containing toluene (100 mg L -1) (MMT) or glucose (MMG) as the sole carbon source, 3 with specific growth rates of 0.019 h -1 and 0.042 h -1, respectively. Scanning (SEM) as well as 4 transmission (TEM) electron microscope analyses showed that the bacterial cells grown to mid 5 log in the presence of toluene possess a plasmolysis space. -
Aerobic and Nitrate Respiration Routes of Carbohydrate Catabolism in Pseudomonas S Tut Zeri
AN ABSTRACT OF THE THESIS OF WILLIAM JAN SPANGLER for the Ph. D. in MICROBIOLOGY (Name) (Degree) (Major) thesis is presented Date 7 / `> /q6! Title AEROBIC AND NITRATE RESPIRATION ROUTES OF CAR- BOHYDRATE CATABOLISM IN PSEUDOMONAS STUTZERI Abstract approved ( Major professor) Pseudomonas stutzeri and other denitrifying bacteria are able to grow under anaerobic conditions, using nitrate -oxygen as the terminal hydrogen acceptor, in a manner analagous to classical aerobic respiration with free -molecular oxygen. This rather unique phenomenon is known as nitrate respiration. Nitrate respiration has been studied with respect to the nitrate reducing enzymes and carrier systems involved in the reduction sequence, but very little emphasis has been placed on the metabolic pathways which are associated with nitrate respiration. This study was carried out in an attempt to establish the metabolic pathways operative, both under aerobic con- ditions and during nitrate respiration, in order to determine whether there was any shift of pathways under conditions of nitrate respira- tion. Primary pathways were determined by the radiorespirometric method using specifically labelled glucose and gluconate. The results, based primarily on the rate of decarboxylation of the C -1 and C -4 positions of glucose, indicated the operation of the Entner- Doudoroff and pentose phosphate pathways under both aerobic condi- tions and conditions of nitrate respiration. Evolution of 14CO2 from the other labels of glucose, as well as incorporation of these labels into the cell, indicated that terminal pathways such as the tricar- boxylic acid cycle or glyoxalate cycle might also be operative under both conditions of oxygen relationship. The secondary pathways were studied using specifically labelled acetate. -
Dissolved Organic Matter-Mediated Photodegradation of Anthracene and Pyrene in Water Siyu Zhao, Shuang Xue*, Jinming Zhang, Zhaohong Zhang & Jijun Sun
www.nature.com/scientificreports OPEN Dissolved organic matter-mediated photodegradation of anthracene and pyrene in water Siyu Zhao, Shuang Xue*, Jinming Zhang, Zhaohong Zhang & Jijun Sun Toxicity and transformation process of polycyclic aromatic hydrocarbons (PAHs) is strongly depended on the interaction between PAHs and dissolved organic matters (DOM). In this study, a 125W high- pressure mercury lamp was used to simulate the sunlight experiment to explore the inhibition mechanism of four dissolved organic matters (SRFA, LHA, ESHA, UMRN) on the degradation of anthracene and pyrene in water environment. Results indicated that the photodegradation was the main degradation approach of PAHs, which accorded with the frst-order reaction kinetics equation. The extent of degradation of anthracene and pyrene was 36% and 24%, respectively. DOM infuence mechanism on PAHs varies depending upon its source. SRFA, LHA and ESHA inhibit the photolysis of anthracene, however, except for SRFA, the other three DOM inhibit the photolysis of pyrene. Fluorescence quenching mechanism is the main inhibiting mechanism, and the binding ability of DOM and PAHs is dominantly correlated with its inhibiting efect. FTIR spectroscopies and UV–Visible were used to analyze the main structural changes of DOM binding PAHs. Generally, the stretching vibration of N–H and C–O of polysaccharide carboxylic acid was the key to afect its binding with anthracene and C–O–C in aliphatic ring participated in the complexation of DOM and pyrene. Polycyclic aromatic hydrocarbons (PAHs) are typical persistent organic pollutants with two or more fused ben- zene rings that are widely distributed in multi-media, such as atmosphere, water, sediment, snow, and biota1–4. -
Study of Ethylenediaminetetraacetic Acid (EDTA)
Indian E-Journal of Pharmaceutical Sciences 01[01] 2015 www.asdpub.com/index.php/iejps ISSN: 2454-5244 (Online) Original Article Zero order and area under curve spectrophotometric methods for determination of Aspirin in pharmaceutical formulation Mali Audumbar Digambar*, Hake Gorakhnath, Bathe Ritesh Department of Pharmaceutics, Sahyadri College of Pharmacy, Methwade, Sangola-413307, Solapur, Maharashtra, India *Corresponding Author Abstract Mali Audumbar Digambar Objective: A simple, accurate, precise and specific zero order and area under curve Department of Pharmaceutics, spectrophotometric methods has been developed for determination of Aspirin in its tablet Sahyadri College of Pharmacy, Methwade, dosage form by using methanol as a solvent. Sangola-413307, Solapur, Maharashtra, India Methods: (1) Derivative Spectrophotometric Methods: The amplitudes in the zero order E -mail: [email protected] derivative of the resultant spectra at 224 nm was selected to find out Aspirin in its tablet dosage form by using methanol as a solvent. (2) Area under curve (Area calculation): The proposed area under curve method involves Keywords: measurement of area at selected wavelength ranges. Two wavelength ranges were selected Aspirin, 218-227 nm for estimation of Aspirin. UV visible Result & Discussion: The linearity was found to be 5-25 μg/ml for Aspirin. The mean % Spectrophotometry, recoveries were found to be 99.47% and 100.43% of zero order derivative and area under AUC, curve method of Aspirin. For Repeatability, Intraday precision, Interday precision, % RSD were Method Validation, found to be 0.6416, 0.0046 and 0.9819, 0.8112 for zero order and 0.7257, 0.8731 and 0.7528, Analgesic, Accuracy. 1.7943 for area under curve method respectively. -
Protection of Α-Tocopherol and Selenium Against Acute Effects of Malathion on Liver and Kidney of Rats
African Journal of Pharmacy and Pharmacology Vol. 5(8). pp. 1054-1062, August, 2011 Available online http://www.academicjournals.org/ajpp DOI: 10.5897/AJPP11.226 ISSN 1996-0816 ©2011 Academic Journals Full Length Research Paper Protection of -tocopherol and selenium against acute effects of malathion on liver and kidney of rats Abdulaziz M. Al-Othman1, Khaled S. Al-Numair1, Gaber E. El-Desoky2,3, Kareem Yusuf2, Zeid A. Al Othman2, Mourad A. M. Aboul-Soud3,4* and John P. Giesy5,6,7,8 1Department of Community Health Sciences, College of College of Applied Medical Science, King Saud University, Kingdom of Saudi Arabia. 2Department of Chemistry, College of Science, King Saud University, Kingdom of Saudi Arabia. 3Biochemistry Department, Faculty of Agriculture, Cairo University, 12613 Giza, Egypt. 4College of Science, King Saud University, P. O. BOX 2245, Riyadh 11451, Kingdom of Saudi Arabia. 5Department of Veterinary Biomedical Sciences and Toxicology Centre, University of Saskatchewan, Saskatoon, Saskatchewan, Canada. 6Department of Zoology, and Center for Integrative Toxicology, Michigan State University, East Lansing, MI, USA. 7School of Biological Sciences, University of Hong Kong, Hong Kong, SAR, China. 8Zoology Department, College of Science, King Saud University, P. O. Box 2455, Riyadh 11451, Saudi Arabia. Accepted 22 July, 2011 Protection from effects of the organophosphate insecticide, malathion on the liver and kidney of male Wistar albino rats by -tocopherol and selenium was investigated. Significantly greater (P<0.01) mean concentrations of malondialdehyde (MDA) and lesser concentrations (P<0.01) of reduced glutathione (GSH) and tissues total proteins were observed in liver and kidney of rats exposed to malathion. -
Isolation and Characterization of a Novel Denitrifying Bacterium with High Nitrate Removal: Pseudomonas Stutzeri
Iran. J. Environ. Health. Sci. Eng., 2010, Vol. 7, No. 4, pp. 313-318 ISOLATION AND CHARACTERIZATION OF A NOVEL DENITRIFYING BACTERIUM WITH HIGH NITRATE REMOVAL: PSEUDOMONAS STUTZERI *1A. Rezaee, 2H. Godini, 1S. Dehestani, 1S. Kaviani 1 Department of Environmental Health, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran 2 Department of Environmental Health, School of Public Health, Lorestan University of Medical Sciences, Khoramabbad, Iran Received 16 August 2009; revised 13 Jully 2010; accepted 20 August 2010 ABSTRACT The aim of this study was to isolate and characterize a high efficiency denitrifier bacterium for reducing nitrate in wastewater. Six denitrifier bacteria with nitrate removal activities were isolated from a petrochemical industry effluent with high salinity and high nitrogen concentrations without treatment. The isolated bacteria were tested for nitrate reomoval activity. One of the bacterium displayed the highest reduction of nitrate. The strain was preliminarily identified using biochemical tests and further identified based on similarity of PCR-16S rRNA using universal primers. Biochemical and molecular experiments showed that the best bacterium with high nitrate removal potential was Pseudomonas stutzeri, a member of the α subclass of the class Proteobacteria. The extent of nitrate removal efficiency was 99% at 200 mg/L NO3 and the nitrite content of the effluent was in the prescribed limit. The experiments showed the ability of Pseudomonas stutzeri to rapidly remove nitrate under anoxic conditions. The strain showed to be potentially good candidate for biodenitrification of high nitrate solutions. Key words: Pseudomonas stutzeri; Denitrification; Polymerase Chain Reaction, Isolation; Characterization INTRODUCTION Biological denitrification is a process carried to respire anaerobically using nitrogen oxides as out by numerous genera of bacteria.