Studies of the NAD metabolism of Haemophilus influenzae

Haemophilus influenzae, as well as other members of the genus which require V-factor, display a unique growth requirement for intact NAD. This organism, the primary cause of bacterial meningitis, is incapable of synthesis of pyridine nucleotides from the usual precursors. An externally directed nu...

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Main Author: Kahn, David W.
Other Authors: Biochemistry and Nutrition
Format: Others
Language:en_US
Published: Virginia Polytechnic Institute and State University 2015
Subjects:
Online Access:http://hdl.handle.net/10919/52297
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spelling ndltd-VTETD-oai-vtechworks.lib.vt.edu-10919-522972021-01-09T05:32:18Z Studies of the NAD metabolism of Haemophilus influenzae Kahn, David W. Biochemistry and Nutrition LD5655.V856 1985.K336 Haemophilus influenzae Bacteria -- Physiology Haemophilus influenzae, as well as other members of the genus which require V-factor, display a unique growth requirement for intact NAD. This organism, the primary cause of bacterial meningitis, is incapable of synthesis of pyridine nucleotides from the usual precursors. An externally directed nucleotide pyrophosphatase was extracted from the organism and purified 700-fold using ammonium sulfate precipitation, ion-exchange and affinity chromatography. The enzyme was determined to be a periplasmic glycoprotein consisting of a single polypeptide of M<sub>r</sub>= 65,000. The enzyme had a pH optimum over the range .pH 8.0-9.0 and was not activated by the addition of mono or divalent cations, nor was it inhibited by EDTA. The enzyme was observed to have a broad substrate specificity and functioned in a manner indicative of negative cooperativity with all substrates except several modified in the adenine ring. The most effective inducer of negative cooperativity was NAD as indicated by its Hill coefficient of 0.26. The enzyme was inhibited by adenine nucleotides _ and 5'-AMP, at 20 μM, abolished the negative cooperativity of the enzyme. The enzyme was determined to possess excitation and emission maxima at 286 and 337 nm, respectively, indicative of the presence of tryptophan. The fluorescence of the enzyme was quenched by addition of aliquots of adenine nucleotides. The quenching occurred in a biphasic manner. The enzyme was inactivated by 2,3- butanedione and by Woodward's Reagent K. Studies of the ability of compounds to serve as V-factor revealed that nicotinamide mononucleotide (NM), NAD, as well as analogs of NAD, served as V-factor. The ability of compounds to inhibit growth was also accessed, and the growth of the organism was seen to be inhibited by adenine nucleotides as well as other compounds. The inhibition of growth of Haemophilus influenzae has important clinical implications which are discussed, as well as a model of the NAD metabolism of the organism which is presented. Ph. D. 2015-05-14T16:36:08Z 2015-05-14T16:36:08Z 1985 Dissertation Text http://hdl.handle.net/10919/52297 en_US OCLC# 12928317 In Copyright http://rightsstatements.org/vocab/InC/1.0/ viii, 186 leaves application/pdf application/pdf Virginia Polytechnic Institute and State University
collection NDLTD
language en_US
format Others
sources NDLTD
topic LD5655.V856 1985.K336
Haemophilus influenzae
Bacteria -- Physiology
spellingShingle LD5655.V856 1985.K336
Haemophilus influenzae
Bacteria -- Physiology
Kahn, David W.
Studies of the NAD metabolism of Haemophilus influenzae
description Haemophilus influenzae, as well as other members of the genus which require V-factor, display a unique growth requirement for intact NAD. This organism, the primary cause of bacterial meningitis, is incapable of synthesis of pyridine nucleotides from the usual precursors. An externally directed nucleotide pyrophosphatase was extracted from the organism and purified 700-fold using ammonium sulfate precipitation, ion-exchange and affinity chromatography. The enzyme was determined to be a periplasmic glycoprotein consisting of a single polypeptide of M<sub>r</sub>= 65,000. The enzyme had a pH optimum over the range .pH 8.0-9.0 and was not activated by the addition of mono or divalent cations, nor was it inhibited by EDTA. The enzyme was observed to have a broad substrate specificity and functioned in a manner indicative of negative cooperativity with all substrates except several modified in the adenine ring. The most effective inducer of negative cooperativity was NAD as indicated by its Hill coefficient of 0.26. The enzyme was inhibited by adenine nucleotides _ and 5'-AMP, at 20 μM, abolished the negative cooperativity of the enzyme. The enzyme was determined to possess excitation and emission maxima at 286 and 337 nm, respectively, indicative of the presence of tryptophan. The fluorescence of the enzyme was quenched by addition of aliquots of adenine nucleotides. The quenching occurred in a biphasic manner. The enzyme was inactivated by 2,3- butanedione and by Woodward's Reagent K. Studies of the ability of compounds to serve as V-factor revealed that nicotinamide mononucleotide (NM), NAD, as well as analogs of NAD, served as V-factor. The ability of compounds to inhibit growth was also accessed, and the growth of the organism was seen to be inhibited by adenine nucleotides as well as other compounds. The inhibition of growth of Haemophilus influenzae has important clinical implications which are discussed, as well as a model of the NAD metabolism of the organism which is presented. === Ph. D.
author2 Biochemistry and Nutrition
author_facet Biochemistry and Nutrition
Kahn, David W.
author Kahn, David W.
author_sort Kahn, David W.
title Studies of the NAD metabolism of Haemophilus influenzae
title_short Studies of the NAD metabolism of Haemophilus influenzae
title_full Studies of the NAD metabolism of Haemophilus influenzae
title_fullStr Studies of the NAD metabolism of Haemophilus influenzae
title_full_unstemmed Studies of the NAD metabolism of Haemophilus influenzae
title_sort studies of the nad metabolism of haemophilus influenzae
publisher Virginia Polytechnic Institute and State University
publishDate 2015
url http://hdl.handle.net/10919/52297
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