Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1954 Sep 20;38(1):41-52.
doi: 10.1085/jgp.38.1.41.

The position of the cell nucleus in pathways of hydrogen transfer: cytochrome C, flavoproteins, glutathione, and ascorbic acid

The position of the cell nucleus in pathways of hydrogen transfer: cytochrome C, flavoproteins, glutathione, and ascorbic acid

H STERN et al. J Gen Physiol. .

Abstract

A study has been made of calf thymus and liver tissue to ascertain the position of the nucleus with respect to mechanisms capable of hydrogen transfer. Although previous work had shown that reduced pyridine nucleotide coenzymes are produced in the course of nuclear metabolism, it has now been established that the flavoprotein system of cytochrome c reductase, cytochrome c, and most, if not all, of other flavoproteins are absent from nuclei. Metabolites capable of cytochrome c reduction, notably ascorbic acid and glutathione, have been demonstrated in the nuclei. Glutathione reductase has been found present in nuclei only to a minor extent, suggesting that nuclear glutathione might function largely in a capacity other than that of hydrogen carrier in the nucleus. Although no enzymatic relation could be established between ascorbic acid and hydrogen transfer in nuclei) it was possible to demonstrate a close association between ascorbic acid concentration and the mitotic process in lily anthers. The significance of the anaerobic character of nuclear metabolism to chromosome function is discussed.

PubMed Disclaimer

References

    1. J Biol Chem. 1952 May;196(1):111-20 - PubMed
    1. Arch Biochem. 1951 Feb;30(2):217-25 - PubMed
    1. Biochem J. 1954 Jan;56(1):44-6 - PubMed
    1. Cancer Res. 1953 Sep;13(9):617-32 - PubMed
    1. J Natl Cancer Inst. 1950 Feb;10(4):983-7 - PubMed