Bacteria and Cyanobacteria

Total Page:16

File Type:pdf, Size:1020Kb

Bacteria and Cyanobacteria Bacteria and Cyanobacteria Bacteria represent an amazingly diverse group of organisms that are of great ecological, economic, agricultural, and medical importance. Cyanobacteria, also known as blue-green bacteria, contain thylakoid membranes with photosynthetic pigments (chlorophyll a and phycobilins) and are capable to oxygenic photosynthesis. Purple bacteria and green sulfur bacteria occupy habitats in the presence of hydrogen sulfide and oxidize and release sulfur gas rather than oxygen. Nitrogen fixing and denitrifying bacteria have an exceptionally important role in nitrogen cycling in terrestrial plant communities. Many vascular plants such as legumes and an aquatic fern have a symbiotic relationship with nitrogen fixing bacteria. Bacteria are also important carbon recyclers in the environment by assisting in the decomposition of dead organisms. Bacteria are considered Prokaryotes (before the nucleus) and represent a lineage that is ancient and possess a number of novel features. Bacteria generally lack internal compartmentalized organelles that are bound by membranes. Organelles such as Golgi bodies (dictyosomes), chloroplasts, mitochondria, and nuclei are regarded as unique to Eukaryotic (true nucleus) organisms. Recently, evolutionary biologists have determined that two major kingdoms of bacteria are present on the planet. Eubacteria represent the true bacteria and contain many of the groups that we are most familiar with such as cyanobacteria. E. coli, Streptococcus, and Rhizobium. Archaebacteria represent an ancient lineage whose members occupy rather inhospitable habitats such as deep sea thermal vents and miles deep in the Earth=s crust, but are also found in more normal environments. The objective of this lab is to examine the morphology, structure, and ecology of bacteria and cyanobacteria. Activity 1. Bacterial Forms A prepared slide of three bacterial forms is provided in the laboratory. Examine the slide by holding it up to the light to identify the three pink stained regions of the slide. Each region possesses a different form of bacteria. You will need to start with the 10X objective to identify these regions and then proceed to the 20X and 40X objectives. 6. In the space below, draw a representative of the three bacterial forms and provide dimensional measurements. You will probably need to review the use of the ocular micrometer from the lab on microscopes and cells. Cocci (sphere-shaped) Bacilli (rod-shaped) width (µm) width (µm) Length (µm) length (µm) Spirilli (spiral-shaped) width µm length µm 103 Comparison of surface area. Using data from the Microscope and Cell Lab, calculate the side surface area of an elodea leaf cell. Calculate a corresponding cell surface area for one bacillus bacterium. Elodea leaf cell Width = μm Length = μm Area = width X length = μm2 Bacillus bacterium Width = μm Length = μm Area = width X length = μm2 How many bacteria would cover the surface area of one elodea leaf cell? If an elodea leaf contained 2000 cells on one surface of the leaf, then how many bacteria could cover the entire leaf? Activity 2. Cyanobacteria (Blue-green bacteria) 104 This group of ancient bacteria may represent the first organisms to produce atmospheric oxygen on Earth. Although they are prokaryotic, cyanobacteria do possess thylakoids and perform oxygenic photosynthesis. They are found in a wide variety of habitats from hot thermal springs at Yellowstone National Park to frigid lakes of Antarctica. Some forms of cyanobacteria grow in the fur of Polar Bears and actually tint the fur green. In central New York, cyanobacteria are common in stagnant water and soil. Cyanobacteria are capable of binding calcium carbonate in unique dome-like deposits called stromatolites. These structures are common in tidal flats of Western Australia. Because they grow slowly and form distinct layers, some stromatolites have been aged to 3-3.5 billion years old. Many species of cyanobacteria are nitrogen fixers like Rhizobium and Azotobacter. Nitrogen fixation occurs in specialized cells with thick cells walls called heterocysts. Nitrogen fixation by the cyanobacterium Anabaena is economically important. You will be presented with several representatives of cyanobacteria. These may include Gleocapsa, Oscillatoria, Spirulina, and Anabaena. Make a wet mount and observe under high power on the light microscope. For each species, please draw the form of the colony; observe the presence/absence of heterocysts, the presence/absence of a protective gelatinous sheath, and the size of individual cells. Gleocapsa Oscillatoria Spirulina Anabaena 105 .
Recommended publications
  • Isolation and Identification of Denitrifying Bacteria and Its Growth and Metabolism Characteristics
    2017 2nd International Conference on Environmental Science and Energy Engineering (ICESEE 2017) ISBN: 978-1-60595-417-2 Isolation and Identification of Denitrifying Bacteria and Its Growth and Metabolism Characteristics Xin-ran JIANG, Dian JIAO, Lei ZHANG and Li-na ZHENG College of Marine Technology and Environmental, Dalian Ocean University, Dalian 116023, China Keywords: Denitrification, Nitrate, Isolation and identification, Activity research. Abstract. A denitrifying bacterium DN20 was isolated from the biofilm after centrifugation in the aquaculture purification system of a aquaculture base, and the denitrification characteristics of the strain were further studied. The strain was identified by 16S rDNA sequence analysis, the effects of temperature, salinity, pH, substrate concentration and C/N ratio on denitrification activity were studied. Introduction Denitrifying bacteria are a kind of bacteria that can cause denitrification. Biological denitrification is the use of denitrifying bacteria, nitrate nitrogen into gaseous products to remove, is considered to be the most economical and effective way of nitrogen removal [1]-[2]. The application of denitrifying bacteria and the removal of nitrate in water have become the research focus[3]-[5], many methods have been reported [6]-[8]. In recent years, some studies on salt tolerant and halophilic denitrifying bacteria have been reported abroad [9]-[10]. In this study, the sludge from the culture pond was taken as the main separation source, and the enrichment, separation and purification were carried out.To obtain a highly efficient nitrate removal ability of denitrifying bacteria, named strain DN20. The aim of this study is to provide effective bacteria source for practical application of nitrate-N treatment in aquaculture water.
    [Show full text]
  • 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.
    [Show full text]
  • Enrichment of Denitrifying Bacterial Community Using Nitrite As an Electron Acceptor for Nitrogen Removal from Wastewater
    water Article Enrichment of Denitrifying Bacterial Community Using Nitrite as an Electron Acceptor for Nitrogen Removal from Wastewater Renda Yao, Quan Yuan and Kaijun Wang * State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, Beijing 100084, China; [email protected] (R.Y.); [email protected] (Q.Y.) * Correspondence: [email protected]; Tel.: +86-10-6278-9411 Received: 31 October 2019; Accepted: 17 December 2019; Published: 20 December 2019 Abstract: This work aimed to enrich a denitrifying bacterial community for economical denitrification via nitrite to provide the basic objects for enhancing nitrogen removal from wastewater. A sequencing batch reactor (SBR) with continuous nitrite and acetate feeding was operated by reasonably adjusting the supply rate based on the reaction rate, and at a temperature of 20 2 C, pH of 7.5 0.2, ± ◦ ± and dissolved oxygen (DO) of 0 mg/L. The results revealed that the expected nitrite concentration can be achieved during the whole anoxic reaction period. The nitrite denitrification rate of nitrogen removal from synthetic wastewater gradually increased from approximately 10 mg/(L h) to 275.35 mg/(L h) over 12 days (the specific rate increased from 3.83 mg/(g h) to 51.80 mg/(g h)). Correspondingly, the chemical oxygen demand/nitrogen (COD/N) ratio of reaction decreased from 7.9 to 2.7. Both nitrite and nitrate can be used as electron acceptors for denitrification. The mechanism of this operational mode was determined via material balance analysis of substrates in a typical cycle. High-throughput sequencing showed that the main bacterial community was related to denitrification, which accounted for 84.26% in the cultivated sludge, and was significantly higher than the 2.16% in the seed sludge.
    [Show full text]
  • Influence of Denitrification in Aquatic Sediments on the Nitrogen Content of Natural Waters J
    6 / c__ Influence of denitrification in aquatic sediments on the nitrogen content of natural waters J. F. van Kessel Influence of denitrification in aquatic sedimentso n the nitrogen content of naturalwater s Proefschrift ter verkrijging van degraa d van doctor in de landbouwwetenschappen, op gezagva n derecto r magnificus, dr. ir. J. P.H .va n derWant , hoogleraar in devirologie , in het openbaar te verdedigen opvrijda g 8oktobe r 1976 desnamiddag s te vier uur in de aula van de Landbouwhogeschool te Wageningen Centrefor Agriculture Publishingand Documentation Wageningen —1976 Abstract Kessel, J. F. van (1976) Influence of denitrification in aquatic sediments on the nitrogen content of natural waters. Agric. Res. Rep. (Versl. landbouwk. Onderz.) 858. Pudoc, Wageningen. ISBN 90 220062 04 . (vi)+ 5 2 p.: 12figs ; 14 tables;Eng .an d Dutch summaries. Forms part of a doctoral thesis, Wageningen ((vii) + 104 p., 43 figs, 28 tables). Other parts are published in Water Research,bu t are summarized in the Agric.Res .Rep . A study was made of microbiological processes, particularly denitrification, leading to the elimi­ nation of nitrogen from natural waters. As denitrification is an anaerobic process and natural waters mostly contain dissolved oxygen, this process was suggested to proceed in the anaerobic sediment at the bottom of natural waters. Two widely differing types of aquatic sediments were tested in the laboratory for effects of temperature, oxygen and nitrate in the overlying water, and thickness of the sediment layer on the rate of denitrification. During disappearance of nitrate from the overlying water, by far most of thenitrat e was converted to molecular nitrogen by denitrification and only a small part of the nitrate was utilized for cell synthesis (immobilization).
    [Show full text]
  • Microbial Function on Climate Change Addis Ababa, Ethiopia – a Review Received: 14 March, 2018 Accepted: 28 April, 2018 Published: 30 April, 2018
    vv ISSN: 2690-0777 DOI: https://dx.doi.org/10.17352/ojeb LIFE SCIENCES GROUP Endeshaw Abatenh*, Birhanu Gizaw, Zerihun Tsegaye and Genene Tefera Review Article Endeshaw Abatenh, Ethiopia Biodiversity Institute, Department of Microbiology, Comoros Street, 0000, Microbial Function on Climate Change Addis Ababa, Ethiopia – A Review Received: 14 March, 2018 Accepted: 28 April, 2018 Published: 30 April, 2018 *Corresponding author: Endeshaw Abatenh, Ethiopia Abstract Biodiversity Institute, Department of Microbiology, Comoros Street, 0000, Addis Ababa, Ethiopia, Greenhouse gases concentration is increased through time within different human and natural E-mail: [email protected] factors. Such as combustion of coal, oil and other fossil fuels, decay of plant matter and biomass burning. Now a day’s climate change and global warming is the major problem in the world. It is damage Keywords: Green House Gases (GHGs); Climate (destroy) a number of biotic componets. It have also effect on microbial comunity stracture, function change; Microbial comunity; Biogeochemical cycle; and their metablolic activity. In order to fi ght (compromize) climate change using a number of methods Methanotropic. are listed here. For example, microorganisms and other biological componets have many potential role https://www.peertechz.com for mitigation by contribute forward response. Microorganisms have a wide function especialy used in greenhouse gas treatment and reduction through nutrient recycling processes. It act as either generators or users of these gases in a good manner. It provide to reduce environment hazards which is caused by nature and antropogenic activity. In overall biogeochemical cycles and climate changes are never see separately. Introduction of a certain region, including temperature, rainfall, and wind.
    [Show full text]
  • Neoproterozoic Iron Formation: an Evaluation of Its Temporal, Environmental and Tectonic Significance
    ÔØ ÅÒÙ×Ö ÔØ Neoproterozoic Iron Formation: An evaluation of its temporal, environmental and tectonic significance Grant M. Cox, Galen P. Halverson, William G. Minarik, Daniel P. Le Heron, Francis A. Macdonald, Eric J. Bellefroid, Justin V. Strauss PII: S0009-2541(13)00349-5 DOI: doi: 10.1016/j.chemgeo.2013.08.002 Reference: CHEMGE 16961 To appear in: Chemical Geology Received date: 2 November 2012 Revised date: 29 July 2013 Accepted date: 5 August 2013 Please cite this article as: Cox, Grant M., Halverson, Galen P., Minarik, William G., Le Heron, Daniel P., Macdonald, Francis A., Bellefroid, Eric J., Strauss, Justin V., Neo- proterozoic Iron Formation: An evaluation of its temporal, environmental and tectonic significance, Chemical Geology (2013), doi: 10.1016/j.chemgeo.2013.08.002 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. ACCEPTED MANUSCRIPT Neoproterozoic Iron Formation: An evaluation of its temporal, environmental and tectonic significance Grant M. Cox 1* , Galen P. Halverson 1, William G. Minarik 1, Daniel P. Le Heron 2, Francis A. Macdonald 3, Eric J. Bellefroid 1, Justin V. Strauss 3 *Corresponding author 1-McGill University, Montreal, Quebec, Canada 2-Royal Holloway, University of London, United Kingdom 3-Harvard University, Massachusetts, U.S.A.
    [Show full text]
  • The Interplay of Microbially Mediated and Abiotic Reactions in the Biogeochemical Fe Cycle
    REVIEWS The interplay of microbially mediated and abiotic reactions in the biogeochemical Fe cycle Emily D. Melton, Elizabeth D. Swanner, Sebastian Behrens, Caroline Schmidt and Andreas Kappler Abstract | Many iron (Fe) redox processes that were previously assumed to be purely abiotic, such as photochemical Fe reactions, are now known to also be microbially mediated. Owing to this overlap, discerning whether biotic or abiotic processes control Fe redox chemistry is a major challenge for geomicrobiologists and biogeochemists alike. Therefore, to understand the network of reactions within the biogeochemical Fe cycle, it is necessary to determine which abiotic or microbially mediated reactions are dominant under various environmental conditions. In this Review, we discuss the major microbially mediated and abiotic reactions in the biogeochemical Fe cycle and provide an integrated overview of biotic and chemically mediated redox transformations. Fe speciation The environmental abundance of iron (Fe) and its pos‑ and temporal distribution of Fe redox species in some Refers to the redox state of session of electrons in d orbitals with π‑character, which environments, such as heterogeneous sediments, plant iron (Fe) and the identity of its can form complexes with carbon (C), oxygen (O), nitro‑ rhizospheres and microbial mats6, and abiotic Fe trans‑ ligands. The two most common gen (N) and sulphur (S) species, make it an essential ele‑ formations with biologically produced intermediates environmental Fe redox ment for nearly all living organisms. Fe occurs in two must be taken into account7,8. species are Fe(II) and Fe(III). main redox states in the environment: oxidized ferric Fe Despite our growing knowledge of the wide‑ (Fe(iii)), which is poorly soluble at circumneutral pH; spread environmental occurrence and the importance and reduced ferrous Fe (Fe(ii)), which is easily soluble of microbial Fe redox cycling for the degradation and and therefore more bioavailable.
    [Show full text]
  • Microbial Cooking, Cleaning, and Control Under Stress
    life Review Housekeeping in the Hydrosphere: Microbial Cooking, Cleaning, and Control under Stress Bopaiah Biddanda 1,* , Deborah Dila 2 , Anthony Weinke 1 , Jasmine Mancuso 1 , Manuel Villar-Argaiz 3 , Juan Manuel Medina-Sánchez 3 , Juan Manuel González-Olalla 4 and Presentación Carrillo 4 1 Annis Water Resources Institute, Grand Valley State University, Muskegon, MI 49441, USA; [email protected] (A.W.); [email protected] (J.M.) 2 School of Freshwater Sciences, University of Wisconsin-Milwaukee, Milwaukee, WI 53204, USA; [email protected] 3 Departamento de Ecología, Facultad de Ciencias, Universidad de Granada, 18071 Granada, Spain; [email protected] (M.V.-A.); [email protected] (J.M.M.-S.) 4 Instituto Universitario de Investigación del Agua, Universidad de Granada, 18071 Granada, Spain; [email protected] (J.M.G.-O.); [email protected] (P.C.) * Correspondence: [email protected]; Tel.: +1-616-331-3978 Abstract: Who’s cooking, who’s cleaning, and who’s got the remote control within the waters blan- keting Earth? Anatomically tiny, numerically dominant microbes are the crucial “homemakers” of the watery household. Phytoplankton’s culinary abilities enable them to create food by absorbing sunlight to fix carbon and release oxygen, making microbial autotrophs top-chefs in the aquatic kitchen. However, they are not the only bioengineers that balance this complex household. Ubiqui- tous heterotrophic microbes including prokaryotic bacteria and archaea (both “bacteria” henceforth), Citation: Biddanda, B.; Dila, D.; eukaryotic protists, and viruses, recycle organic matter and make inorganic nutrients available to Weinke, A.; Mancuso, J.; Villar-Argaiz, primary producers. Grazing protists compete with viruses for bacterial biomass, whereas mixotrophic M.; Medina-Sánchez, J.M.; protists produce new organic matter as well as consume microbial biomass.
    [Show full text]
  • And Phytoplankton Community Compositions Related in Lakes Differing in Their Cyanobacteria Contribution and Physico-Chemical Properties?
    G C A T T A C G G C A T genes Article Are Bacterio- and Phytoplankton Community Compositions Related in Lakes Differing in Their Cyanobacteria Contribution and Physico-Chemical Properties? Mikołaj Kokoci ´nski 1,*, Dariusz Dziga 2 , Adam Antosiak 2 and Janne Soininen 3 1 Department of Hydrobiology, Faculty of Biology, Adam Mickiewicz University, Uniwersytetu Pozna´nskiego 6, 61-614 Pozna´n,Poland 2 Laboratory of Metabolomics, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Krakow, Poland; [email protected] (D.D.); [email protected] (A.A.) 3 Department of Geosciences and Geography, University of Helsinki, P.O. Box 64, FIN-00014 Helsinki, Finland; janne.soininen@helsinki.fi * Correspondence: [email protected] Abstract: Bacterioplankton community composition has become the center of research attention in recent years. Bacteria associated with toxic cyanobacteria blooms have attracted considerable interest. However, little is known about the environmental factors driving the bacteria community, including the impact of invasive cyanobacteria. Therefore, our aim has been to determine the relationships be- tween heterotrophic bacteria and phytoplankton community composition across 24 Polish lakes with different contributions of cyanobacteria including the invasive species Raphidiopsis raciborskii. This Citation: Kokoci´nski,M.; Dziga, D.; analysis revealed that cyanobacteria were present in 16 lakes, while R. raciborskii occurred in 14 lakes. Antosiak, A.; Soininen, J. Are Bacterio- Our results show that bacteria communities differed between lakes dominated by cyanobacteria and and Phytoplankton Community lakes with minor contributions of cyanobacteria but did not differ between lakes with R. raciborskii Compositions Related in Lakes and other lakes.
    [Show full text]
  • Anammox – a Novel Microbial Process for Ammonium Removal
    RESEARCH NEWS Anammox – A novel microbial process for ammonium removal N. Shivaraman and Geetha Shivaraman Anammox1,2, a process of anaerobic Recently7 it was discovered that anam- moxasome is believed to be surrounded ammonium oxidation, is an innovative mox makes a significant (up to 70%) by a bilayer membrane that consists of technological advancement in the removal contribution to nitrogen cycling in the unique ‘ladderane’ lipids5. of ammonia nitrogen in waste water. world’s oceans. Figure 1 shows the The structure and function of anam- This new process combines ammonia and involvement of anammox process in the mox lipids has been published recently10. nitrite directly into dinitrogen gas3. The biological nitrogen cycle including meta- Lipid membranes are essential to the anammox reaction can be represented as bolic pathway for anaerobic ammonium functioning of cells facilitating the exis- + - NH 4 + NO 2 = N2 + 2H2O. This reaction oxidation. tence of concentration gradients of ions is carried out by anammox bacteria be- Initially anammox research5 was fo- and metabolites. Microbial membrane longing to the planctomycete group. Bac- cused on the basic properties of the proc- lipids are known to contain three-, five-, teria capable of anaerobically oxidizing ess and on providing evidence for its six-, and even seven-membered aliphatic ammonia were not identified earlier and microbial nature and the principles of the rings, but four-membered aliphatic cyclo- were known as ‘lithotrophs missing from nitrogen and carbon metabolism. It butane rings have been reported for the 4. Subsequently, this missing lith- appears that the anammox process is first time, in the dominant membrane otroph was discovered1 and identified as based on energy conservation from an- lipids of two anammox bacteria.
    [Show full text]
  • Ecology of N2O Reducing Bacteria in Arable Soils Luiz A
    Ecology of N2O reducing bacteria in arable soils Luiz A. Domeignoz Horta To cite this version: Luiz A. Domeignoz Horta. Ecology of N2O reducing bacteria in arable soils. Bacteriology. Université de Bourgogne, 2016. English. NNT : 2016DIJOS031. tel-01494970 HAL Id: tel-01494970 https://tel.archives-ouvertes.fr/tel-01494970 Submitted on 24 Mar 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Thèse de Doctorat Ecole Doctorale Environnement-Santé Écologie des bactéries N2O réductrices dans les sols agricoles LUIZ A. DOMEIGNOZ HORTA Écologie des bactéries N2O réductrices dans les sols agricoles Thèse de Doctorat Soutenue le 16 Décembre 2016 à Dijon LUIZ A. DOMEIGNOZ HORTA Mme Lydie CHAPUIS-LARDY, IRD, Montpellier, France Rapporteur M. Xavier LE ROUX, INRA, Lyon, France Rapporteur M. Denis ANGERS, AAC/AAFC, Québec, Canada Examinateur M. David WENDEHENNE, INRA, Dijon, France Examinateur M. Laurent PHILIPPOT, INRA, Dijon, France Directeur de thèse M. Aymé SPOR, INRA, Dijon, France Co-encadrant de thèse Université de Bourgogne Ecole Doctorale Environnement Santé Dijon, France INRA UMR 1347 Agroécologie Dijon, France Abstract Nitrous oxide (N2O) is an important greenhouse gas (GHG) and the main ozone depleting substance.
    [Show full text]
  • Nitrogen Removal Using Arkea®
    1 ® OWEA 2013 Technical Conference and Exposition June 18 – 21, 2013 Michael H. Gerardi ArchaeaSolutions, Inc. www.archaeasolutions.com [email protected] 2 Nitrogenous Wastes in Domestic Wastewater • Urine ▫ Urea as major component of urine ▫ Chemical formula: NH2COH2N ▫ Urea contains two (2) amine groups (-NH2) ▫ Urea is hydrolyzed in the sewer system ▫ Hydrolysis results in the release of reduced + nitrogen (NH4 /NH3) 3 Dominant Form of Reduced Nitrogen as Determined by pH 100 0 % % + NH3 NH4 50 50 0 100 pH 7 pH 9 pH 11 4 Nitrogenous Wastes in Domestic Wastewater Feces Proteins (organic-nitrogen) as a major component Proteins made of amino acids Amino acids contain amine groups (-NH2) Deamination of proteins and degradation of amino acids in sewer system and aeration tank results in the release of amine groups and the release of + 3 reduced nitrogen (NH4 /NH ) Therefore, organic-nitrogen represents bonded nitrogen (amine groups) that may/must be released in aeration tank 5 Amino acid, cysteine HSCH2CHNH2COOH Amine group + - - NH3/NH4 /NO2 /NO3 Thiol group - 2- H2S/H2S/HS /SO4 H2S (1 to 3 mg/L) toxic to nitrifying microbes 6 Free and Organic-Nitrogen • Free reduced nitrogen + ▫ NH4 /NH3 in solution ▫ Determined by ammonia testing • Organic-nitrogen ▫ Bonded nitrogen that may/must be released ▫ Determined by total Kjeldahl nitrogen (TKN) and ammonia testing: TKN – NH3 7 Archaeal and Bacterial Roles in Nitrification and Denitrification • Remove soluble cBOD • Provide maximum time for nitrification • Provide acceptable nitrification
    [Show full text]