Improved Fixation of Cellulose-Acetate Reverse-Osmosis Membrane for Scanning Electron Microscopy

Similar documents
BIOLOGICAL SAMPLE PREPARATION FOR TEM OBSERVATION. TEM Seminar Nov 16, 2017 Astari Dwiranti, Ph.D

COPYRIGHTED MATERIAL. Tissue Preparation and Microscopy. General Concepts. Chemical Fixation CHAPTER 1

A Comparison of Techniques Useful for Preparing Nematodes for Scanning Electron Microscopy 1

Methods of Culturing Microorganisms. Chapter 3. Five Basic Techniques of Culturing Bacteria. Topics

Technical Overview Cross-linking fixatives: What they are, what they do, and why we use them

Transmission Electron Microscopic Study of Antibiotic Action on Klebsiella pneumoniae Biofilm

Conditions Critical for Optimal Visualization of Bacteriophage

CHAPTER 1. Aspects of the Three-Dimensional Intracellular Organization of Mesocarp Cells as Revealed by Scanning Electron Microscopy

Scanning electron microscopy of corneal wound healing in the rabbit. Barrett G. Haik and Marilyn L. Zimny

C. acetobutyricum. Initial co-culture. Transfer 1

Foundations in Microbiology Seventh Edition

Introduction to Electron Microscopy Andres Kaech

ELECTRONIC SUPPLEMENTARY INFORMATION (ESI)

How to perform a Gram Stain. Jasleen Singh

Improved Monitoring of P. aeruginosa on Agar Plates

to take a full thickness biopsy of epidermis, dermis and hypodermis. phosphate buffer) for conventional EM and/ or in paraformaldehyde for immuno-em

Vampirococcus sucking on Chromatium

Visualization of the real microarchitecture of glycoprotein matrices with scanning electron microscopy

EXPERIMENT 4 STAINING TECHNIQUES

Immuno-Labelling Cryosections

A HIGH-YIELD TECHNIQUE FOR PREPARING CELLS FIXED

How to Get Well-Preserved Samples for Transmission Electron Microscopy

Reverse Osmosis. Lecture 17

JOURNALS REPORTS NEWSLETTERS BOOKS registration prices about help

Monday: Y42 G53 Tuesday: Y42 G53 Wednesday: Y42 J11

Methods: General Techniques OEST 740

SEM (SCANNING ELECTRON MICROSCOPE)

Supplementary Information

Use of Quantitative Scanning Electron Microscopy of S. aureus Biofilm Formation in vitro to Identify Strain and Implant Material Specificities

Supplementary Materials and Methods

Improved Method of Embedding with Epoxy Resin 'Quetol

Scanning Electron Microscope Study of Pseudomonas fragi on

Biomimetic cell-mediated three-dimensional assembly of halloysite nanotubes

Principles Governing Microbe-Mineral Interfacial Phenomena

Microbiology Chapter 2 Laboratory Equipment and Procedures 2:1 The Light Microscope MICROSCOPE: any tool with a lens to magnify and observe tiny

Microtexture measurement of copper damascene line with EBSD

QX-102 Applications Manual

SEM Immunocytochemistry for Cells & Materials

1 The role of scanning electron microscopy in cell and molecular biology: SEM basics, past accomplishments, and new frontiers

Biofilm as a new bio-material

Written By: Madison Calvert, Amanda Hernandez, Natalie Sorial, Sarina Spolidoro, Benjamin Spenciner

INVESTIGATIVE OPHTHALMOLOGY. Critical point drying of soft biological material for the scanning electron microscope

Biofilms 101 Remediation Strategies in Meat Processing

ULTRASTRUCTURAL STUDIES ON THE SURFACE MEMBRANE OF THE MOUSE EGG

Supporting Information

Specimen Preparation Technique for a Microstructure Analysis Using the Focused Ion Beam Process

3.2 Test for sterility

PRESENCE OF WIDESPREAD BACTERIAL ATTACKS IN PRESERVATIVE-TREATED COOLING TOWER TIMBERS

Independent Student Research Project MICROBIAL DIVERSITY 1994 MBL, WOODS HOLE ILKA FAATH UNIVERSITY OF BONN GERMANY

Prelinzirwry and Short Report

Electron Microscopy of Adhesive Interactions between GavdneveZIa naginah and Vaginal Epithelial Cells, McCoy Cells and Human Red Blood Cells

Simple method for formation of nanometer scale holes in membranes. E. O. Lawrence Berkeley National Laboratory, Berkeley, CA 94720

Dark-Field Electron Microscopy of Thin Sections of

Rapid processing of renal glomeruli for electron microscopy

by JAKOB R~LI and PER R. FLOOD, Institute of Anatomy, University of Bergen, 5000 Bergen, Norway Paper accepted 4 November 1977

Scanning Electron Microscopy

Rumen Bacterial Degradation of Forage Cell Walls Investigated by Electron Microscopy

STRUCTURE OF LANDMARK LOOP RIBONUCLEOPROTEIN MATRICES IN PLEURODELES WALTLII LAMPBRUSH CHROMOSOMES VISUALIZED BY SCANNING ELECTRON MICROSCOPY

Chapter 10: Classification of Microorganisms

Filamentous Bacteria

Scanning Electron Microscope Examination of Airxchange Enthalpy Exchange Surface

Introduction to Histology

Benefits and limitations of steam cleaner for the biocleaning of surfaces

Keywords : Bacterial cellulose, Dielectric barrier discharge (DBD) plasma, Gelatin, Acetobacter xylinum ABSTRACT

Supporting Information

Specimen Preparation Techniques for Scanning Electron Microscopy of Developing Peanut Pegs' H. E. Pattee', S. C. Mohapatra3 and E. K.

Heng-Pan Yang, Sen Qin, Ying-Na Yue, Li Liu, Huan Wang* and Jia-Xing Lu**

studies of human intestinal mucosa

Staining and Embedding the Whole Mouse Brain for Electron Microscopy

MOISTURE REQUIREMENTS OF BACTERIA

Sputter Coating. Technical Brief

PLASMONIC STRUCTURES IN PMMA RESIST

Effects of Substrate Morphology on Osteoblastic Response to Thin Film Calcium Phosphate Coatings F. Horgan 1, B.J. Meenan 1 1

Protein-Pak Hi Res HIC Column and HIC Protein Standard

Morphological Investigations - Different Microscopic Techniques (Semicrystalline Polymers)

NANOGOLD PRODUCT INFORMATION

CHAPTER 7 MICRO STRUCTURAL PROPERTIES OF CONCRETE WITH MANUFACTURED SAND

MICROBIOLOGICALLY INFLUENCED CORROSION ANALYSIS ON CARBON STEEL COUPONS

rios Water Purification system The standard for laboratory-grade water

Scanning Electron Microscopic Study of Uropathogen Adherence to a Plastic Surface

Wastewater Treatment in a Hybrid Biological Reactor (HBR) : Nitrification Characteristics 1

Supplementary material (ESI) for Journal of Materials Chemistry This journal is The Royal Society of Chemistry 2009

Samples of fluorescent and non-fluorescent specimens of Montastraea cavernosa were

Scanning Electron Microscopy of Cristispira Species in

Histological preparation of embryonic and adult zebrafish eyes

Introduction to Histology

Electronic Supplementary Information Motorized. Janus Metal Organic Framework Crystals

PREPARATION OF NEODYMIUM HYDROXIDE NANORODS AND NEODYMIUM OXIDE NANORODS BY A HYDROTHERMAL METHOD

PREPARATION OF HISTOLOGICAL SPECIMENS

Supplementary Information for. Fast Analysis of Intracellular Glucose at Single Cells using Electrochemiluminescence Imaging

Summary of Issues Strategies Benefits & Costs Key Uncertainties Additional Resources

THE MAGNITUDE OF THE EXTRACELLULAR SPACE IN ELECTRON MICROGRAPHS OF SUPERFICIAL AND DEEP REGIONS OF THE CEREBRAL CORTEX

RNAstorm FFPE. RNA Isolation Kit for FFPE Tissue Samples. Kit Manual. 20 extractions (CD201) 50 extractions (CD501) rev. 1.3

Polymer Microscopy. Second edition LINDA C. SAWYER. and. DAVID T. GRUBB Cornell University Ithaca, NY USA. Hoechst Celanese Corporation Summit, NJ USA

Selective Sensing and Imaging of Penicillium italicum Spores and Hyphae using Carbohydrate-Lectin Interactions

Samples Conductive and Observations on the Surface Morphology of Human Erythrocytes and Ehrlich Ascites Cells*

Methodology for Immunohistochemistry. Learning Objectives:

Examination of Virus-Infected Cultured Cells

Transcription:

APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Feb. 1985, p. 446450 0099-2240/85/020446-05$02.00/0 Copyright 1985, American Society for Microbiology Vol. 49, No. 2 Improved Fixation of Cellulose-Acetate Reverse-Osmosis Membrane for Scanning Electron Microscopy S. M. KUTZ,' D. L. BENTLEY,2 AND N. A. SINCLAIR'* Department of Microbiology and Immunologyl and Electron Microscope Facility, College of Agriculture,2 University of Arizona, Tucson, Arizona 85721 Received 6 August 1984/Accepted 15 November 1984 Fixation of cellulose-acetate membranes with either glutaraldehyde-osmium tetroxide or glutaraldehyde-ruthenium tetroxide resulted in extensive electron beam damage. Beam damage was eliminated and the bacterial surface structure was preserved, however, when cellulose-acetate membranes were fixed with glutaraldehyderuthenium tetroxide and treated successively with thiocarbohydrazide and osmium tetroxide. Scanning electron microscopy (SEM) is a valuable tool for evaluating biofilm formation and biodegradation of celluloseacetate (CA) reverse-osmosis membranes used in water and advanced wastewater treatment. SEM has been used in previous studies to determine biofilm thickness and composition as well as to reveal chlorine-induced lesions in CA membranes (8, 9). In addition, SEM allows visualization of the microenvironment within reverse-osmosis units and provides information on the characteristics of bacteria present. Glycocalyx networks and bacterial stalks or appendages are indirect evidence of bacterial colonization and adherence. SEM sample preparation often involves the use of glutaraldehyde or glutaraldehyde followed by osmium tetroxide fixation (2). The material is then dehydrated in an ethanol series, critical point dried, and coated with gold or a goldpalladium alloy. CA membranes processed in this way are readily damaged by an electron beam. Destruction of the CA occurs even at low accelerating voltages (5 to 10 kv) and low magnifications (<5,000x) (8). Optimum focusing and correction for astigmatism are severely limited. Details of bacterial fine structure and the overall physical condition of the CA membrane surface cannot be discerned at high magnifications (>5,000x) because of electron beam lability. The application of additional coatings of a gold-palladium alloy to CA membranes does not alleviate beam damage. The purpose of this research was to develop a method for the fixation and preservation of CA membrane integrity for SEM analysis. Membranes fixed with glutaraldehyde and treated successively with ruthenium tetroxide, thiocarbohydrazide, osmium tetroxide, thiocarbohydrazide, and osmium tetroxide (RTOTO) were scanned at high and low magnifications at accelerating potentials of 10 to 30 kv. For comparative purposes, CA membranes were fixed with glutaraldehyde and treated with either ruthenium tetroxide or osmium tetroxide. The electron beam damage to CA membranes and attached microorganisms was assessed. Three strips (2 by 5 cm) of a low-pressure CA membrane (degree of substitution, 2.67) were used as the sole carbon source for naturally occurring well water bacteria inoculated into flasks of 0.1% Bacto-Peptone (Difco Laboratories, Detroit, Mich.). Cultures were incubated for 2 weeks at 25 C. The CA strips were then fixed overnight in 4% glutaraldehyde (Electron Microscopy Sciences, Ft. Wash- * Corresponding author. ington, Pa.) in 0.1 M Millonig buffer (5) at ph 7.2. Samples were rinsed three times for 5 minutes each time in Millonig buffer, followed by three five-minute washes in high-pressure-liquid-chromatography (HPLC)-grade water. The first CA strip was postfixed for 30 min in 2% osmium tetroxide (EMS, Ft. Washington, Pa.) and then rinsed nine times in HPLC-grade water. The second CA strip was postfixed for 30 min in 1% ruthenium tetroxide (Polysciences, St. Louis, Mo.) and rinsed nine times in HPLC-grade water. The third CA strip was treated like the second but in addition was incubated for 30 min in a saturated thiocarbohydrazide solution (Sigma Chemical Co., St. Louis, Mo.). Immediately before use, thiocarbohydrazide was suspended in water and allowed to stand for 1 h at 50 C. The liquid was decanted, and the procedure was repeated until the resulting saturated solution was a clear straw color. The solution was allowed to cool to room temperature before use (6). After being treated with thiocarbohydrazide, the CA strip was washed nine times in HPLC-grade water, incubated in 2% osmium tetroxide for 30 min, and then washed again. Treatments in the thiocarbohydrazide and osmium tetroxide solutions were repeated once (4). All three samples were dehydrated through an ethanol series (30 to 100%) and critical point dried with CO2 (1). The samples were sputter coated with 30 nm of gold-palladium alloy (target composition, 60% Au-40% Pd) with a magnetron sputtering device. Samples were observed with an International Scientific Instruments DS-130 scanning electron microscope. Caution must be used when handling osmium tetroxide and ruthenium tetroxide. Only HPLC-grade water should be used in the preparation of aqueous solutions, and glassware must be free from organic compounds to avoid rapid reduction of ruthenium tetroxide. CA membranes conventionally fixed in glutaraldehydeosmium tetroxide (Fig. 1) were labile, as evidenced by rapid electron beam damage and tearing of the membranes at 20 kv. Beam damage to samples occurred in less than 1 min at magnifications greater than 2,000x and limited the amount of detail visible. Use of a lower accelerating voltage (10 kv) improved the situation somewhat; however, moderate beam damage still occurred in less than 1 min (Fig. 2). Although postfixation with ruthenium tetroxide increased sample stability, beam damage was nevertheless encountered (Fig. 3 and 4). Photographs at magnifications near 5,000x could be attained only by rapid focusing on an adjacent area. Recoat- 446

VOL. 49, 1985 NOTES 447 FIG. 1. Scanning electron micrograph of a CA membrane fixed with 4% glutaraldehyde and postfixed with 2% osmium tetroxide. Accelerating voltage, 20 kv. FIG. 2. Scanning electron micrograph of a CA membrane fixed with 4% glutaraldehyde and postfixed with 2% osmium tetroxide. Accelerating voltage, 10 kv.

448 NOTES APPL. ENVIRON. MICROBIOL. FIG. 3. Scanning electron micrograph of a CA membrane fixed with 4% glutaraldehyde and postfixed with 1% ruthenium tetroxide. Accelerating voltage, 20 kv. FIG. 4. Scanning electron micrograph of a CA membrane fixed with 4% glutaraldehyde and postfixed with 1% ruthenium tetroxide. Accelerating voltage, 10 kv.

VOL. 49, 1985 NOTES 449 FIG. 5. Scanning electron micrograph of a CA membrane fixed with 4% glutaraldehyde and postfixed by the RTOTO method (see text for details). Accelerating voltage, 10 kv. FIG. 6. Scanning electron micrograph of a CA membrane showing attached microorganisms. The sample was fixed with 4% glutaraldehyde and postfixed by the RTOTO method (see text for details). Accelerating voltage, 20 kv.

450 NOTES ing the samples with gold-palladium did not improve the stability. In contrast, CA membranes treated with RTOTO tolerated accelerating potentials from 10 kv (Fig. 5) to 30 kv at magnifications exceeding 30,OOOx for periods of 5 min and longer with no detectable signs of beam damage (Fig. 6). As shown, microbial fine structure was preserved. As no discernable electron beam damage was produced, RTOTO samples could be examined for future reference if desired. Once damaged, areas on conventionally prepared membrane samples cannot be reevaluated. The RTOTO method markedly enhanced the stability of CA membranes. The use of osmium tetroxide for postfixation of electron microscopic samples is well documented; however, osmium tetroxide does not react chemically with most saturated and nonsaturated polymers and polysaccharides, including CA (3). Ruthenium tetroxide, on the other hand, reacts strongly with these compounds, as well as with polar lipids, glycogen, and monosaccharides (3). Rapid darkening of CA membranes as the ruthenium tetroxide is reduced during postfixation is evidence of the binding of the heavy metal ruthenium to the sample (6). However, like osmium tetroxide, ruthenium tetroxide alone cannot effectively reduce electron beam damage of CA membranes. For this reason, thiocarbohydrazide was used as a mordant or ligand for successive postfixation with a combination of ruthenium tetroxide and osmium tetroxide treatments. Its use with osmium tetroxide to produce conductive coatings is well documented (2, 4, 6, 7). However, its use with ruthenium tetroxide to stabilize otherwise electron-beam-labile material is not evident from the literature. Our results show that RTOTO postfixation markedly improved CA membrane stability and preserved microbial fine structure. LITERATURE CITED APPL. ENVIRON. MICROBIOL. 1. Anderson, T. F. 1951. Techniques for preservation of three-dimensional structure in preparing specimens for the electron microscope. Trans. N.Y. Acad. Sci. 13:130-134. 2. Hayat, M. A. 1978. Introduction to biological scanning electron microscopy, p. 242-243. University Park Press, Baltimore. 3. Hayat, M. A. 1981. Fixation for electron microscopy. Academic Press, Inc., New York. 4. Kelley, R. O., A. F. Dekker, and J. G. Bluemink. 1975. Thiocarbohydrazide mediated osmium binding: a technique for protecting soft biological specimens in the scanning electron microscope, p. 34-44. In M. A. Hayat (ed.), Principles and techniques of scanning electron microscopy, vol. 4. Van Nostrand Reinhold Co., New York. 5. Millonig, G. 1976. Laboratory manual of biological electron microscopy. Mario Saviolo, Vercelli, Italy. 6. Murphy, J. A. 1978. Non-coating techniques to render biological specimens conductive, p. 175-193. In R. P. Becker and 0. Johari (ed.), Scanning electron microscopy 1978: international review of advances in techniques and applications of the scanning electron microscope, 1978, part II. Scanning Electron Microscopy, Inc., Chicago, Ill. 7. Murphy, J. A. 1980. Non-coating techniques to render biological specimens conductive/1980 update, p. 209-220. In 0. Johari (ed.), Scanning electron microscopy 1980, part I. Scanning Electron Microscopy, Inc., Chicago, Ill. 8. Ridgway, H. F., C. A. Justice, C. Whittaker, D. G. Argo, and B. H. Olson. 1984. Biofilm fouling of RO membranes-its nature and effect on treatment of water for reuse. Am. Water Works Assoc. J. 76:94-102. 9. Ridgway, H. F., A. Kelly, C. Justice, and B. H. Olson. 1983. Microbial fouling of reverse-osmosis membranes used in advanced wastewater treatment technology: chemical, bacteriological, and ultrastructural analyses. Appl. Environ. Microbiol. 45:1066-1084.