Module 5: Disinfection and Chlorination
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Enhanced Conversion Oflactose to Glycerol by Kluyveromyces Fragilis
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Mar. 1989, p. 573-578 Vol. 55, No. 3 0099-2240/89/030573-06$02.00/0 Copyright C) 1989, American Society for Microbiology Enhanced Conversion of Lactose to Glycerol by Kluyveromyces fragilis Utilizing Whey Permeate as a Substrate WHEAMEI JENQ,1 RAY A. SPECKMAN,' RICHARD E. CRANG,2* AND MARVIN P. STEINBERG1 Department of Food Science, 1304 West Pennsylvania Avenue,' and School of Life Sciences, 505 South Goodwin Avenue,2 University ofIllinois, Urbana, Illinois 61801 Received 6 June 1988/Accepted 12 December 1988 Kluyveromycesfragilis (CBS 397) is a nonhalophilic yeast which is capable of lactose utilization from whey permeate and high glycerol production under anaerobic growth conditions. However, the optimum yields of glycerol (11.6 mg/ml of whey permeate medium) obtained in this study occurred only in the presence of 1% Na2SO3 as a steering agent. The use of other concentrations of Na2SO3, as well as 5% NaCl and 1% ascorbic acid, had no or detrimental effects on cell growth, lactose utilization, and glycerol production. Glycerol yields were greater in cultures grown from a light inoculum of K. fragilis than in cultures in which a resuspended mass of cells was introduced into the medium. The results of this study suggest that this strain of K. fragilis may be useful commercially in the utilization of cheese whey lactose and the concomitant production of glycerol. Cheese whey represents a commercial by-product gener- troleum derivatives, which is less expensive than processing ated in such massive quantities that its safe disposal is a by sugar fermentation. major problem for many municipal sewage treatment plants. -
Sodium Chlorite Neutralization
® Basic Chemicals Sodium Chlorite Neutralization Introduction that this reaction is exothermic and liberates a If sodium chlorite is spilled or becomes a waste, significant amount of heat (H). it must be disposed of in accordance with local, state, and Federal regulations by a NPDES NaClO2 + 2Na2SO3 2Na2SO4 + NaCl permitted out-fall or in a permitted hazardous 90.45g + 2(126.04g) 2(142.04g) + 58.44g waste treatment, storage, and disposal facility. H = -168 kcal/mole NaClO2 Due to the reactivity of sodium chlorite, neutralization for disposal purposes should be For example, when starting with a 5% NaClO2 avoided whenever possible. Where permitted, solution, the heat generated from this reaction the preferred method for handling sodium could theoretically raise the temperature of the chlorite spills and waste is by dilution, as solution by 81C (146F). Adequate dilution, discussed in the OxyChem Safety Data Sheet thorough mixing and a slow rate of reaction are (SDS) for sodium chlorite in Section 6, important factors in controlling the temperature (Accidental Release Measures). Sodium chlorite increase (T). neutralization procedures must be carried out only by properly trained personnel wearing Procedure appropriate protective equipment. The complete neutralization procedure involves three sequential steps: dilution, chlorite Reaction Considerations reduction, and alkali neutralization. The dilution If a specific situation requires sodium chlorite to step lowers the strength of the sodium chlorite be neutralized, the chlorite must first be reduced solution to 5% or less; the reduction step reacts by a reaction with sodium sulfite. The use of the diluted chlorite solution with sodium sulfite to sodium sulfite is recommended over other produce a sulfate solution, and the neutralization reducing agents such as sodium thiosulfate step reduces the pH of the alkaline sulfate (Na2S2O3), sodium bisulfite (NaHSO3), and solution from approximately 12 to 4-5. -
DNA Methylation Analysis: Choosing the Right Method
biology Review DNA Methylation Analysis: Choosing the Right Method Sergey Kurdyukov 1,* and Martyn Bullock 2 Received: 8 July 2015; Accepted: 22 December 2015; Published: 6 January 2016 Academic Editor: Melanie Ehrlich 1 Genomics Core facility, Kolling Institute of Medical Research, University of Sydney, Sydney 2065, Australia 2 Cancer Genetics Laboratory, Kolling Institute of Medical Research, University of Sydney, Sydney 2065, Australia; [email protected] * Correspondence: [email protected]; Tel.: +61-299-264-756 Abstract: In the burgeoning field of epigenetics, there are several methods available to determine the methylation status of DNA samples. However, choosing the method that is best suited to answering a particular biological question still proves to be a difficult task. This review aims to provide biologists, particularly those new to the field of epigenetics, with a simple algorithm to help guide them in the selection of the most appropriate assay to meet their research needs. First of all, we have separated all methods into two categories: those that are used for: (1) the discovery of unknown epigenetic changes; and (2) the assessment of DNA methylation within particular regulatory regions/genes of interest. The techniques are then scrutinized and ranked according to their robustness, high throughput capabilities and cost. This review includes the majority of methods available to date, but with a particular focus on commercially available kits or other simple and straightforward solutions that have proven to be useful. Keywords: DNA methylation; 5-methylcytosine; CpG islands; epigenetics; next generation sequencing 1. Introduction DNA methylation in vertebrates is characterized by the addition of a methyl or hydroxymethyl group to the C5 position of cytosine, which occurs mainly in the context of CG dinucleotides. -
University of Cincinnati
UNIVERSITY OF CINCINNATI DATE: July 5, 2002 I, Dinesh Kumar Palaniswamy , hereby submit this as part of the requirements for the degree of: Master of Science in: Environmental Engineering It is entitled: Electrochemical Reduction of 2,4,6-Trinitrotoluene Approved by: Dr.George Sorial Dr.Dionysios Dionysiou Dr.Makram Suidan ELECTROCHEMICAL REDUCTION OF 2,4,6 -TRINITROTOLUENE A thesis submitted to the Division of Research and Advanced Studies of the University of Cincinnati in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE in the Department of Civil and Environmental Engineering of the college of Engineering 2002 by Dinesh Kumar Palaniswamy B.E., Civil Engineering, P.S.G College of Technology, Coimbatore, 1998 Committee Chair: Dr. George Sorial ABSTRACT 2,4,6-trinitrotoluene (TNT) is a major constituent of munitions contaminated wastewater. This research aims at studying the efficiency of electrochemical processes in reducing TNT. A laboratory scale reactor was designed and developed to electrochemically reduce TNT in simulated munition wastewater. Experiments simulating batch conditions were first conducted on the laboratory scale reactor to study the effect of various parameters including applied current, type of electrolyte and the molar concentration of the electrolyte in the feed solution on the reduction kinetics of TNT. The results showed that the reduction rates of TNT increased with an increase in applied current and molar concentration of electrolyte in feed. The rates of reduction leveled off at higher currents (250 & 300 mA). Mass transfer limitations were speculated for this flattening of rate constants at higher currents. Experimental studies were conducted with two types of electrolyte in the feed- sodium sulfate (Na2SO4) and lithium sulfate (Li2SO4), and the results indicated that there was no significant difference in the reduction rates for TNT. -
Sulfur Dioxide and Some Sulfites, Bisulfites and Metabisulfites
SULFUR DIOXIDE AND SOME SULFITES, BISULFITES AND METABISULFITES 1. Exposure Data 1.1 Chemical and physical data 1.1.1 Synonyms and structural and molecular data Sulfr dioxi Chem. Abstr. Serv Reg. No.: 7446-09-5 Replaced CAS Nos.: 8014-94-6; 12396-99-5; 83008-56-4; 89125-89-3 Chem. Abstr. Name; Sulfur dioxide IUPAC Systematic Name: Sulfur dioxide Synonyms: Sulfurous acid anhydride; sulfurous anhydride; sulfurous oxide; sulfur oxide (S02); sulfur superoxide; sulphur dioxide 0=8=0 S02 MoL. wt: 64.07 Sodium sulfte Chem. Abstr. Serv Reg. No.: 7757-83-7 Altemate CAS No.: 10579-83-6 Replaced CAS No.: 68135-69-3 Chem. Abstr. Name: Sulfurous acid, di sodium salt IUPAC Systematic Name: Sulfurous acid, disodium salt Synonyms: Anhydrous sodium sulfite; disodium sulfite; sodium sulphite o 1/ Na · 0 - 8 - 0 · Na Na2S0J MoL. wt: 126.04 Sodium bisulfe Chem. Abstr. Serv Reg. No.: 7631-90-5 Replaced CAS Nos.: 57414-01-4; 69098-86-8; 89830-27-3; 91829-63-9 Chem. Abstr. Name: Sulfurous acid, monosodium salt IUPAC Systematic Name: Sulfurous acid, monosodium salt -131- 132 lARe MONOGRAPHS VOLUME 54 Synonyms: Hydrogen sulfite sodium; monosodium sulfite; sodium acid sulfite; sodium bisulphite; sodium hydrogen sulfite; sodium sulfite (NaHS03) o Il HO - S - a · Na NaHS03 MoL. wt: 104.06 Sodium metabisulfte Chem. Abstr. Serv Reg. No.: 7681-57-4 Altemate CAS No.: 7757-74-6 Replaced CAS No.: 15771-29-6 Chem. Abstr. Name: Disulfurous acid, disodium salt IUPAC Systematic Name: Pyrosulfurous acid, disodium salt Synonyms: Disodium disulfite; disodium metabisulfite; disodium pyrosulfite; sodium disulfite; sodium metabisulphite; sodium pyrosulfite oIl Il0 Na · 0- S - a - S - a · Na .Na2S20S MoL. -
Synthesis of New Betaine-Type Amphoteric Surfactants from Tall Oil Fatty Acid
J Wood Sci (2002) 48:419424 The Japan Wood Research Society 2002 Shi-Fa Wang Takeshi Furuno Zhi Cheng Synthesis of new betaine-type amphoteric surfactants from tall oil fatty acid Received: August 13, 2001 / Accepted: November 14, 2001 Abstract Two new betaine-type amphoteric surfactants moistening and foaming abilities. It can be widely used - betaine N,N-dihydroxyethyl-N-ethyl fatty acid ester in many fields, such as the chemical, textile, dye, pigment, and ammonium N-(fatty acid ester) ethyl-N,N-bis (2- food, pharmaceutical, machining, metallurgy, washing, and hydroxyethyl)-3-(2-hydroxypropyl) sulfonate - were syn- petroleum industries. It has been used as a detergent, moist- thesized using tall oil fatty acids as the raw materials. ening and foaming agent, corrosion inhibitor, dispersion Processing conditions suitable for synthesizing the inter- agent, germicide (bactericide), emulsifying agent, antistatic mediates and final products were probed. In addition, the and softening agent of fibers, a dye, a chelating agent, and a chemical structures of the intermediates and the final prod- cleaning agentY ucts were identified by infrared spectroscopy, hydrogen A betaine-type surfactant usually means that quaternary nuclear magnetic resonance spectroscopy, and elemental ammonium cationic groups and anionic groups such as analysis. --COO-, --SO3, --OSO3, and --PO2 coexist in the same molecule. It has excellent solubility over a wide range of pH Key words Tall oil fatty acid Amphoteric surfactant values. Its solubility does not obviously decrease even in an Betaine type isoelectric zone. In addition, unlike the external quaternary ammonium salt, the betaine-type surfactant is compatible with ionic surfactants. Among the betaine-type surfactants, Introduction the most important contain sulfonic and carboxylic groups because they have important commercial value and a wide application field. -
In Bisulfite/Permanganate for Organic Compounds Oxidation
Water Research 148 (2019) 198e207 Contents lists available at ScienceDirect Water Research journal homepage: www.elsevier.com/locate/watres New insight into the reactivity of Mn(III) in bisulfite/permanganate for organic compounds oxidation: The catalytic role of bisulfite and oxygen * Shifa Zhong, Huichun Zhang Department of Civil Engineering, Case Western Reserve University, 2104 Adelbert Road, Cleveland, OH, 44106-7201, USA article info abstract À À Article history: A recently discovered bisulfite(HSO3 )/permanganate(MnO4 ) system was reported to produce highly Received 24 June 2018 reactive free Mn(III) that can oxidize organic compounds in milliseconds. However, this characteristic Received in revised form reactivity was not found in all other known reaction systems that can also produce free Mn(III). Why can 18 September 2018 Mn(III) in NaHSO /KMnO be so active? Here, we found NaHSO and O acted as catalysts for the reaction Accepted 12 October 2018 3 4 3 2 between Mn(III) and organic compounds. Without O , 0% of organic compounds were oxidized in Available online 23 October 2018 2 NaHSO3/KMnO4, indicating the absence of O2 inactivated Mn(III) reactivity. When the reaction between NaHSO and KMnO was monitored in air, Mn(III) catalyzed rapid oxidation of NaHSO by O . Then, the Keywords: 3 4 3 2 Bisulfite and permanganate Mn(III) that could oxidize organic compounds was found to be the ones involved in the catalytic reaction Bisulfite/oxygen reaction between NaHSO3 and O2, thus the link between O2 and Mn(III) reactivity was established. Finally, Disproportionation NaHSO3/O2 can be viewed as catalysts for the reaction between Mn(III) and organic compounds because Mn(III) catalyst 1) when Mn(III) was involved in oxidizing organic compounds, it stopped being the catalyst for the Mn(III) oxidant reaction between NaHSO3 and O2 so that they were consumed to a much smaller extent; and 2) without Water treatment NaHSO3 and O2, Mn(III) lost its oxidation ability. -
Winemaking Basics-Bruce Hagen.Pdf
Winemaking Basics Bruce Hagen Sourcing grapes: good wine starts with good grapes Ripeness: is generally expressed as percent sugar or °Brix (°B). The normal range is 22 – 26°B (17.5 to 19 for sparkling and 21 for some ‘crisp’ and austere whites). Use a hydrometer or a refractometer to check it. If you harvest much above 26, you should consider diluting the juice (must) with water to adjust it to downward a bit, depending on the alcohol level you are comfortable with. The problem with making wines from high °Brix grapes is that the resulting alcohol level will be high. The fermentation may stop (stick) and the wine may taste hot. Therefore, you should consider diluting the must or juice, if the sugar level is much above 26 (see adjusting the °Brix below). The alcohol conversion factor for most yeasts is about .57, but ranges from .55 to as high as .64. Multiply the °B by the conversion factor to determine the probable alcohol level: ex 26°B x .57 = 14.8%. If the °B level is 27, the resulting alcohol level will be 15.4 —very hot! If you dilute to 25, the alcohol will be 14.25%. If you dilute it to 24ºB, the alcohol will be 13.7% —quite acceptable. Whites vs. reds: § White grapes are de-stemmed, crushed, and pressed before fermentation. § Skin contact is relatively short. § Red grapes are typically de-stemmed, crushed, cold-soaked (optional), and he wine pressed off the skins and seeds after fermentation. Skin contact is lengthy, so color and tannins are more intense. -
Website Exposure May Cause Bronchitis to Develop with Coughing, ( Or in Your Facility’S RTK Phlegm, And/Or Shortness of Breath
Right to Know Hazardous Substance Fact Sheet Common Name: SODIUM BISULFITE Synonym: Sodium Hydrogen Sulfite CAS Number: 7631-90-5 Chemical Name: Sulfurous Acid, Monosodium Salt RTK Substance Number: 1685 Date: August 1998 Revision: April 2008 DOT Number: UN 2693 (Solution) Description and Use EMERGENCY RESPONDERS >>>> SEE BACK PAGE Sodium Bisulfite is a white, crystalline solid with a slight odor Hazard Summary of rotten eggs. It is often in a liquid solution. It is used in Hazard Rating NJDOH NFPA making paper and leather, as a food preservative and in dye HEALTH 2 - and chemical production. FLAMMABILITY 0 - REACTIVITY 0 - CORROSIVE POISONOUS GASES ARE PRODUCED IN FIRE Reasons for Citation f Sodium Bisulfite is on the Right to Know Hazardous Substance List because it is cited by ACGIH, DOT, NIOSH, Hazard Rating Key: 0=minimal; 1=slight; 2=moderate; 3=serious; 4=severe IARC and EPA. f This chemical is on the Special Health Hazard Substance List. f Sodium Bisulfite can affect you when inhaled. f Contact can severely irritate and burn the skin and eyes. f Inhaling Sodium Bisulfite can irritate the nose, throat and lungs. f Sodium Bisulfite may cause a skin allergy and an asthma- like allergy. SEE GLOSSARY ON PAGE 5. f Sodium Bisulfite is CORROSIVE when in a liquid solution with water. FIRST AID Eye Contact f Quickly brush off excess chemical from the face. Immediately flush with large amounts of water for at least 60 Workplace Exposure Limits minutes, lifting upper and lower lids. Remove contact NIOSH: The recommended airborne exposure limit (REL) is lenses, if worn, while flushing. -
Safety Data Sheet SODIUM BISULFITE
Safety Data Sheet SODIUM BISULFITE Section 1 - Product and Company Identification Product Name: Sodium Bisulfite Chemical Formula: NaHSO3 CAS Number: 007631-90-5 Other Designations: Sodium Bisulfite Solution, Sodium Hydrogen Sulfite Solution. General Use: Food and pharmaceutical preservative, waste water dechlorination agent, laboratory reagent, reducing agent, dietary supplement, and color preservative. Manufacturer: INEOS Calabrian Corporation 5500 Hwy. 366 Port Neches, Texas77651 Telephone: 409-727-1471 Fax: 409-727-5803 Emergency Contact: CHEMTREC 800-424-9300 Section 2 - Hazards Identification Emergency Overview Target Organs: Respiratory system, eyes, skin GHS Classification: Acute Toxicity, Oral (Category 4) Acute Toxicity, Dermal (Category 5) Serious Eye Irritant (Category 2A) GHS Label Elements: Signal Word – Warning Pictogram Corrosive Irritant Hazard Statements: H302 – Harmful if swallowed H313 – May be harmful to skin H319 – Causes serious eye irritation Precautionary P280 – Wear protective equipment for hands, eyes, face and respiratory tract Statements: P305, P351 and P338 – IF IN EYES: Rinse with water for several minutes. Remove contact lenses if present and continue rinsing. Other Hazards: Contact with acids liberates toxic sulfur dioxide gas. HMIS Classification: Health Hazard 2 Flammability 0 Physical 0 1 Safety Data Sheet SODIUM BISULFITE NFPA Rating: Health Hazard 2 Fire 0 Reactivity 0 Potential Health Inhalation: Irritant to respiratory tract Effects: Eye: Irritant Skin: Irritant Ingestion: Harmful if swallowed Aggravated Medical Condition: Capable of provoking bronchospasm in sulfite sensitive individuals with asthma. Section 3 - Composition / Information on Ingredients Composition CAS Number % Wt Water - 50 – 70 Sodium bisulfite 007631-90-5 30 – 50 Sodium Sulfite 007757-83-7 < 1.0 Sodium Sulfate 007757-82-6 < 3.5 Section 4 - First Aid Measures Exposure Route Symptom Treatment Inhalation: Sore throat, shortness of Remove from exposure to fresh air. -
Azobenzene-P-Phenylhydrazine Sulfonic Acid and Its Reactions
AZOBENZENE-p -PHENYLHYDRAZINE SULFONIC ACID AND ITS REACTIONS BY WALTER FRED STRAUB THESIS FOR THE DEGREE OF BACHELOR OF SCIENCE IN CHEMISTRY COLLEGE OF LIBERAL ARTS AND SCIENCES UNIVERSITY OF ILLINOIS 1918 UNIVERSITY OF ILLINOIS *3 June 1 8 THIS IS TO CERTIFY THAT THE THESIS PREPARED UNDER MY SUPERVISION BY Walter.. .Zred...S.traub..... ENTITLED....Aj5Sfo.8tt3.e^^ actions IS APPROVED BY ME AS FULFILLING THIS P ART OF THE REQUIREMENTS FOR THE „.S ie , C h i t ry, DEGREE OF £a or .. of c n c e ... in em s Instructor in Charge HEAD OF DEPARTMENT OF TABLE OF COUNTS Page PART I. I Introduction 1 II Historical Part 3 III Theoretical Part 7 (A) The Reaction of the Formation of Azobenzene- p-phenylhydrazine Sulfonic Acid 8 (B) Condensations of the Red Acid 1. With aromatic aldehydes and ketones. 9 2. With aliphatic aldehydes and ketones. 10 3. With sugars to form osazones, 11 4. With acetoacetic ester. 12 5. With dihydroxytartarie acid. 13 IV Experimental Part 14 (A) Preparation of Azobenzene-p-phenylhydrazine Sulfonic Acid 14 (B) Identification of the Acid. 15 (G) Preparation and Analysis of: G H 01 18 18 22W H 1I 18 °30 30 8 4 -' G H 1J ^ ma:1 tose condensation) 19 36 40 8°9 ( lac1;ose condensation) 20 G 36H40%°9 21 C 1SH20H4°2 21 C18HS0°2H4HC1 (D) Condensation with Dihydroxytartarie Acid 22 1. Preparation of dihydroxytartarie acid 22 2. Condensation in glacial acetic acid solution 23 Y Summary 24 PART II. Some Rosin Compounds 26 Rosin derivatives prepared "by: 1. -
Kinetic and Structural Studies Reveal a Unique Binding Mode of Sulfite to The
Kinetic and structural studies reveal a unique binding mode of sulfite to the nickel center in urease Luca Mazzei1, Michele Cianci2, Stefano Benini3, Leonardo Bertini1, Francesco Musiani1, Stefano Ciurli1* 1 Laboratory of Bioinorganic Chemistry, Department of Pharmacy and Biotechnology, University of Bologna, Via Giuseppe Fanin 40, I-40138, Bologna (Italy) 2 European Molecular Biology Laboratory c/o DESY, Notkestraße 85, 22607 Hamburg, Germany 3 Bio-Organic Chemistry and Bio-Crystallography Laboratory, Faculty of Science and Technology, Free University of Bolzano, Piazza Università 5, 39100 Bolzano, Italy * Corresponding author: [email protected]; phone: (+39)-051-209-6204; fax: (+39)-051-209-6203 1 ABSTRACT Urease is the most efficient enzyme known to date, and catalyzes the hydrolysis of urea using two Ni(II) ions in the active site. Urease is a virulence factor in several human pathogens, while causing severe environmental and agronomic problems. Sporosarcina pasteurii urease has been used extensively in the structural characterization of the enzyme. Sodium sulfite has been widely used as a preservative in urease solutions to prevent oxygen-induced oxidation, but its role as an inhibitor has also been suggested. In the present study, isothermal titration microcalorimetry was used to establish sulfite as a competitive inhibitor for S. pasteurii urease, with an inhibition constant of 0.19 mM at pH 7. The structure of the urease-sulfite complex, determined at 1.65 Å resolution, shows the inhibitor bound to the dinuclear Ni(II) center of urease in a tridentate mode involving bonds between the two Ni(II) ions in the active site and all three oxygen atoms of the inhibitor, supporting the observed competitive inhibition kinetics.