» Articles » PMID: 14044953

HEMIN BIOSYNTHESIS IN HAEMOPHILUS

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1963 Apr 1
PMID 14044953
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

White, David C. (The Rockefeller Institute, New York, N.Y.) and S. Granick. Hemin biosynthesis in Haemophilus. J. Bacteriol. 85:842-850. 1963.-Hemin-independent Haemophilus species have been shown to form hemin by the classical hemin biosynthetic pathway. Three distinct species of Haemophilus [H. influenzae, H. aegyptius, and H. canis (H. haemoglobinophilus)] all lost the enzymatic capacities to convert delta-aminolevulinic acid to protoporphyrin, which accounts for their dependence on hemin for growth. The strain of H. aegyptus tested cannot form hemin from protoporphyrin, can be transformed with deoxyribonucleic acid (DNA) from H. influenzae, and the resultant progeny have the enzymatic activity to convert protoporphyrin to hemin. Attempts to transform these species to hemin independence with DNA from hemin-independent H. parainfluenzae are unsuccessful under conditions where streptomycin resistance is readily transformed.

Citing Articles

Sedimentary Cobalt Protoporphyrin as a Potential Precursor of Prosthetic Heme Group for Bacteria Inhabiting Fossil Organic Matter-Rich Shale Rock.

Stasiuk R, Matlakowska R Biomolecules. 2021; 11(12).

PMID: 34944556 PMC: 8699415. DOI: 10.3390/biom11121913.


Biosynthesis of Tetrapyrrole Cofactors by Bacterial Community Inhabiting Porphyrine-Containing Shale Rock (Fore-Sudetic Monocline).

Stasiuk R, Krucon T, Matlakowska R Molecules. 2021; 26(21).

PMID: 34771152 PMC: 8587615. DOI: 10.3390/molecules26216746.


In Vitro Anti-NTHi Activity of Haemophilin-Producing Strains of .

Atto B, Latham R, Kunde D, Gell D, Tristram S Pathogens. 2020; 9(4).

PMID: 32218184 PMC: 7238096. DOI: 10.3390/pathogens9040243.


Novel antimicrobial activities of a peptide derived from a Japanese soybean fermented food, Natto, against Streptococcus pneumoniae and Bacillus subtilis group strains.

Kitagawa M, Shiraishi T, Yamamoto S, Kutomi R, Ohkoshi Y, Sato T AMB Express. 2017; 7(1):127.

PMID: 28641406 PMC: 5479777. DOI: 10.1186/s13568-017-0430-1.


The Detection of Hemin-Binding Proteins in Riemerella anatipestifer CH-1.

Liao H, Liu M, Cheng X, Zhu D, Wang M, Jia R Curr Microbiol. 2015; 72(2):152-158.

PMID: 26542531 DOI: 10.1007/s00284-015-0932-5.


References
1.
Bogorad L . The enzymatic synthesis of porphyrins from porphobilinogen. II. Uroporphyrin III. J Biol Chem. 1958; 233(2):510-5. View

2.
White D, Smith L . Hematin enzymes of Hemophilus parainfluenzae. J Biol Chem. 1962; 237:1332-6. View

3.
Leidy G, JAFFEE I, Alexander H . Emergence of competence (for transformation) of three Hemophilus species in a chemically defined environment. Proc Soc Exp Biol Med. 1962; 111:725-31. DOI: 10.3181/00379727-111-27904. View

4.
LASCELLES J . The synthesis of enzymes concerned in bacteriochlorophyll formation in growing cultures of Rhodopseudomonas spheroides. J Gen Microbiol. 1960; 23:487-98. DOI: 10.1099/00221287-23-3-487. View

5.
Elliott W . Aminoacetone formation by Staphylococcus aureus. Biochem J. 1960; 74:478-85. PMC: 1204245. DOI: 10.1042/bj0740478. View