𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Pyridine nucleotide metabolism in mammalian cells in culture

✍ Scribed by David Hillyard; M. C. Rechsteiner; Baldomero M. Olivera


Publisher
John Wiley and Sons
Year
1973
Tongue
English
Weight
950 KB
Volume
82
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The biosynthesis of pyridine nucleotides has been examined in a number of mammalian cell lines in culture. In all lines examined, nicotinamide is incorporated by a biochemical pathway distinct from the Preiss‐Handler pathway for nicotinic acid.

In at least the human cell line D98/AH2, there is no detectable endogenous synthesis of the pyridine ring from tryptophan. Although most cell lines examined (hamster BHK 21/13, mouse L929 and human D98/AH2) use either nicotinic acid or nicotinamide as a precursor for DPN and TPN, two mouse cell lines, 3T3‐4E and LM CIID, are unable to utilize nicotinic acid as a source of the pyridine ring.

If nicotinic acid is present in the medium, substantial amounts of intracellular desamido DPN accumulate suggesting that the last step (desamido DPN→DPN) is limiting in the Preiss‐Handler pathway. With nicotinamide, the only compound which accumulates in substantial amounts apart from DPN and TPN is nicotinamide ribose; there is no detectable NMN. The results of pulse‐labeling experiments suggest that nicotinamide ribose may be an intermediate in the nicotinamide pathway.

Following growth of D98/AH2 cells in high concentrations of niacin, biosynthesis of DPN from nicotinamide was completely inhibited for at least six hours. The converse experiment revealed no inhibition of niacin incorporation. This observation suggests that a niacin pathway intermediate, which present evidence indicates is desamido‐DPN. can inhibit nicotinamide utilization.

Newly synthesized DPN turns over with a half‐life of two hours in azaserine‐treated D98/AH2 cells. In the absence of azaserine, the nicotinamide moiety of newly synthesized DPN is lost from D98/AH2 cells to the medium with a half‐life of eight hours. About 80% of the nicotinamide is lost to medium as nicotinamide ribose.


📜 SIMILAR VOLUMES


Autoradiographic studies of pyridine nuc
✍ Martin Rechsteiner; Keith Lund; David Hillyard; Baldomero Olivera 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 English ⚖ 892 KB

## Abstract More than 80% of the intracellular pyridine metabolite pool of human culture cells is trapped by OsO~4~ fixation. The fixed pyridine metabolites fully exchange with nicotinamide and nicotinic acid but not with nicotinamide adenine dinucleotide. Yet, chromatography of the exchanged compo

Pyridine nucleotide metabolism in mitoti
✍ George Elliott; Martin Rechsteiner 📂 Article 📅 1975 🏛 John Wiley and Sons 🌐 English ⚖ 790 KB

The biosynthesis and turnover of nicotinamide adenine dinucleotide (NAD) have been examined in mitotic cells of the human culture line, D98/AH2. N o significant difference in the incorporation of nicotinic acid or nicotinamide could be detected between mitotic and interphase cells. The distribution

Pyridine nucleotide synthesis in 3T3 cel
✍ Elaine L. Jacobson; Richard A. Lange; Myron K. Jacobson 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 English ⚖ 591 KB

## Abstract The biosynthesis of NAD has been examined in 3T3 cells. The net synthesis of pyridine nucleotides does not occur when cells are cultured in the absence of performed pyridine ring compounds; however, growth continues normally for up to four cell doublings resulting in cells with a total

Multiple steady states with distinct cel
✍ Anna F. Europa; Anshu Gambhir; Peng-Cheng Fu; Wei-Shou Hu 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 179 KB 👁 3 views

Mammalian cells have the ability to proliferate under different nutrient environments by utilizing different combinations of the nutrients, especially glucose and the amino acids. Under the conditions often used in in vitro cultivation, the cells consume glucose and amino acids in great excess of wh

Proline oxidase in cultured mammalian ce
✍ Sylvia J. Downing; Dr. James M. Phang; Edward M. Kowaloff; David Valle; Robert J 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 516 KB

## Abstract We sought a cultured cell line with Proline Oxidase activity to study the regulation and physiologic role of the enzyme in mammalian tissues. Among the cell lines tested, only LLC‐RK~1~ cells, derived from rabbit kidney, had significant Proline Oxidase activity; the K~m~ for proline of