scholarly journals Reaction of Sodium Hypochlorite with Nucleic Acids and Their Constituents

1971 ◽  
Vol 19 (10) ◽  
pp. 2189-2192 ◽  
Author(s):  
HIKOYA HAYATSU ◽  
SHOEKUNG PAN ◽  
TYUNOSIN UKITA
Keyword(s):  
Nucleic Acids ◽  
Sodium Hypochlorite

scholarly journals Chlorine and its importance in the inactivation of bacteria, can it inactivate viruses?

2021 ◽  
Vol 39 (4) ◽  
Author(s):  
Laila Nayzzel Muñoz-Castellanos ◽  
Alejandra Borrego-Loya ◽  
Cindy Viviana Villalba-Bejarano ◽  
Román González-Escobedo ◽  
Nuvia Orduño-Cruz ◽  
...  
Keyword(s):  
Amino Acids ◽  
Nucleic Acids ◽  
Sodium Hypochlorite ◽  
Active Ingredient ◽  
Hypochlorous Acid ◽  
Cell Damage ◽  
Membrane Components ◽  
Fast Acting ◽  
Sulfur Containing ◽  
Inactivation Of Bacteria

Sodium hypochlorite (NaClO) and its active ingredient, hypochlorous acid (HClO), are the most widely used chlorine-based disinfectants. HClO is a fast-acting antimicrobial that interacts with many biomolecules, including amino acids, lipids, nucleic acids, and sulfur containing membrane components, causing cell damage. In this review, we present examples of the effectiveness of chlorine in general disinfection procedures to inactivate bacteria and, under some conditions, bacteria in biofilms and viruses.

scholarly journals Comparisons of Protocols for Decontamination of Environmental Ice Samples for Biological and Molecular Examinations

2004 ◽  
Vol 70 (4) ◽  
pp. 2540-2544 ◽  
Author(s):  
S. O. Rogers ◽  
V. Theraisnathan ◽  
L. J. Ma ◽  
Y. Zhao ◽  
G. Zhang ◽  
...  
Keyword(s):  
Nucleic Acids ◽  
Comparative Study ◽  
Sodium Hypochlorite ◽  
Ice Cores ◽  
Glacial Ice

ABSTRACT Drilling and laboratory manipulations of glacial ice cores introduce contemporary microbes and biomolecules onto the cores. We report herein a systematic comparative study of several decontamination protocols. Only treatment with 5% sodium hypochlorite eliminated all external contaminating microbes and nucleic acids while maintaining the integrity of those within the cores.

scholarly journals Effectiveness of different methods of preparing seedlings of cereals under sterile conditions for investigations of nucleic acids using radioactive precursors

2015 ◽  
Vol 44 (3) ◽  
pp. 361-368
Author(s):  
W. Filek
Keyword(s):  
Nucleic Acids ◽  
Sodium Hypochlorite ◽  
Cetyltrimethylammonium Bromide ◽  
Sodium Lauryl Sulphate ◽  
Fresh Weight ◽  
Wheat Seedlings ◽  
Solid Substratum ◽  
Number Of Bacteria

On seedlings grown from grain not sterilized in advance bacteria numbered more than 10<sup>8</sup> microorganisms per one gram of fresh weight. Washing of seedlings with cetyltrimethylammonium bromide or sodium lauryl sulphate solutions reduced the number of bacteria several times. Sterilization of grains prior to planting with sodium hypochlorite and germination on solid substratum (perlit) reduced the number of bacteria to below 10<sup>4</sup> microorganisms to one gram of fresh weight. If germination was, however, in water, bacteria on the seedlings were approximately as numerous as on seedlings from mon-sterilized grains. Of the three antibiotics tested (streptomycin, chloramphenicol, penicillin) the most effective against the bacteria of wheat seedlings was chloramphenicol coupled with streptomycin; of antibiotics used singly chloramphenicol was best.

Comparison of Acrylamide and Agar Gels by Freeze-Etching

1977 ◽  
Vol 35 ◽  
pp. 606-607
Author(s):  
Russell L. Steere ◽  
Eric F. Erbe
Keyword(s):  
Electron Microscope ◽  
Sodium Hydroxide ◽  
Sodium Hypochlorite ◽  
Chromic Acid ◽  
Distilled Water ◽  
Thin Sheets ◽  
Acid Cleaning ◽  
Agar Gels ◽  
Freeze Etching ◽  
Water Cut

Thin sheets of acrylamide and agar gels of different concentrations were prepared and washed in distilled water, cut into pieces of appropriate size to fit into complementary freeze-etch specimen holders (1) and rapidly frozen. Freeze-etching was accomplished in a modified Denton DFE-2 freeze-etch unit on a DV-503 vacuum evaporator.* All samples were etched for 10 min. at -98°C then re-cooled to -150°C for deposition of Pt-C shadow- and C replica-films. Acrylamide gels were dissolved in Chlorox (5.251 sodium hypochlorite) containing 101 sodium hydroxide, whereas agar gels dissolved rapidly in the commonly used chromic acid cleaning solutions. Replicas were picked up on grids with thin Foimvar support films and stereo electron micrographs were obtained with a JEM-100 B electron microscope equipped with a 60° goniometer stage.Characteristic differences between gels of different concentrations (Figs. 1 and 2) were sufficiently pronounced to convince us that the structures observed are real and not the result of freezing artifacts.

Electron Microscopy of Nucleic Acids

1974 ◽  
Vol 32 ◽  
pp. 302-303
Author(s):  
Norman Davidson
Keyword(s):  
Electron Microscopy ◽  
Nucleic Acids ◽  
Basic Protein ◽  
Molecular Biologist ◽  
Topological Properties ◽  
Protein Film ◽  
Polynucleotide Chain

The basic protein film technique for mounting nucleic acids for electron microscopy has proven to be a general and powerful tool for the working molecular biologist in characterizing different nucleic acids. It i s possible to measure molecular lengths of duplex and single-stranded DNAs and RNAs. In particular, it is thus possible to as certain whether or not the nucleic acids extracted from a particular source are or are not homogeneous in length. The topological properties of the polynucleotide chain (linear or circular, relaxed or supercoiled circles, interlocked circles, etc. ) can also be as certained.

Freeze-Etch Crystal-Like Structures in Membranous Glomerulosclerosis

1969 ◽  
Vol 27 ◽  
pp. 394-395
Author(s):  
Burton B. Silver
Keyword(s):  
Electron Microscopy ◽  
Light Microscopy ◽  
Sodium Hypochlorite ◽  
Kidney Tissue ◽  
Extraction Process ◽  
Donor Kidney ◽  
Unknown Substance ◽  
Etched Surface ◽  
Standard Fixation ◽  
Diseased Kidney

Tissue from a non-functional kidney affected with chronic membranous glomerulosclerosis was removed at time of trnasplantation. Recipient kidney tissue and donor kidney tissue were simultaneously fixed for electron microscopy. Primary fixation was in phosphate buffered gluteraldehyde followed by infiltration in 20 and then 40% glycerol. The tissues were frozen in liquid Freon and finally in liquid nitrogen. Fracturing and replication of the etched surface was carried out in a Denton freeze-etch device. The etched surface was coated with platinum followed by carbon. These replicas were cleaned in a 50% solution of sodium hypochlorite and mounted on 400 mesh copper grids. They were examined in an Siemens Elmiskop IA. The pictures suggested that the diseased kidney had heavy deposits of an unknown substance which might account for its inoperative state at the time of surgery. Such deposits were not as apparent in light microscopy or in the standard fixation methods used for EM. This might have been due to some extraction process which removed such granular material in the dehydration steps.

Isolation of Asbestos from Lung Tissue and Sputum

1982 ◽  
Vol 40 ◽  
pp. 330-331
Author(s):  
M. G. Williams ◽  
C. Corn ◽  
R. F. Dodson ◽  
G. A. Hurst
Keyword(s):  
Sodium Hypochlorite ◽  
Lung Tissue ◽  
Body Fluids ◽  
Unknown Etiology ◽  
The Past

During this century, interest in the particulate content of the organs and body fluids of those individuals affected by pneumoconiosis, cancer, or other diseases of unknown etiology developed and concern was further prompted with the increasing realization that various foreign particles were associated with or caused disease. Concurrently particularly in the past two decades, a number of methods were devised for isolating particulates from tissue. These methods were recently reviewed by Vallyathan et al. who concluded sodium hypochlorite digestion was both simple and superior to other digestion procedures.

mRNA localization by Electron microscopic in situ hybridization

1991 ◽  
Vol 49 ◽  
pp. 430-431
Author(s):  
J. A. Pollock ◽  
M. Martone ◽  
T. Deerinck ◽  
M. H. Ellisman
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Nucleic Acids ◽  
Recombinant Dna ◽  
Light And Electron Microscopy ◽  
Electron Microscopic ◽  
High Voltage Electron Microscopy ◽  
Functional Sites ◽  
Voltage Electron

Localization of specific proteins in cells by both light and electron microscopy has been facilitate by the availability of antibodies that recognize unique features of these proteins. High resolution localization studies conducted over the last 25 years have allowed biologists to study the synthesis, translocation and ultimate functional sites for many important classes of proteins. Recently, recombinant DNA techniques in molecular biology have allowed the production of specific probes for localization of nucleic acids by “in situ” hybridization. The availability of these probes potentially opens a new set of questions to experimental investigation regarding the subcellular distribution of specific DNA's and RNA's. Nucleic acids have a much lower “copy number” per cell than a typical protein, ranging from one copy to perhaps several thousand. Therefore, sensitive, high resolution techniques are required. There are several reasons why Intermediate Voltage Electron Microscopy (IVEM) and High Voltage Electron Microscopy (HVEM) are most useful for localization of nucleic acids in situ.

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