1952
DOI: 10.1126/science.116.3018.483
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Putrescine as a Growth Requirement for Neisseria

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Cited by 49 publications
(13 citation statements)
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“…Putrescine is known to be an essential growth factor for some organisms (18)(19)(20)(21), and may be essential for growth of some organisms in vaginal flora. As shown in Table III, putrescine was produced in vitro by anaerobe(s) in the vaginal flora of patients with NSV.…”
Section: Discussionmentioning
confidence: 99%
“…Putrescine is known to be an essential growth factor for some organisms (18)(19)(20)(21), and may be essential for growth of some organisms in vaginal flora. As shown in Table III, putrescine was produced in vitro by anaerobe(s) in the vaginal flora of patients with NSV.…”
Section: Discussionmentioning
confidence: 99%
“…3,3 '-Diaminodipropylamine, spermidine, spermine, putrescine, agmatine and diaminopropane were found to be active, while the closely related compounds ornithine, diaminoethane, cadaverine and arcain did not promote growth (Herbst, Glinos & Amundsen, 1955). Similarly, putrescine, spermidine, agmatine and cadaverine have been found to stimulate the growth of the bacterium Neisseria (Martin, Pelczar & Hansen, 1952), and putrescine and cadaverine stimulated the growth of bacteria in the genus V e i l k l l a (Rogosa & Bishop, 1964). Spermidine and spermine were growth factors for lactic acid bacteria, but in this case neither putrescine nor diaminopropane were found to be effective (Kihara & Snell, 1957;Guirard & Snell, 1964).…”
Section: )mentioning
confidence: 99%
“…Polyamines stabilize nucleic acids (90) and appear to be involved in some aspects of protein biosynthesis (87,91,92). Some organisms have an absolute requirement for polyamines (83)(84)(85) while polyamine-deficient mutant strains of E. coli can grow indefinitely, but at a lower rate, in their absence (86). Since decarboxylation of S-adenosylmethionine may be the rate-limiting step of mammalian polyamine biosynthesis (75,80,88) and increased activity of the decarboxylase is often associated with cell proliferation (59), the enzyme is considered a potential target for cancer chemotherapy (89).…”
Section: Metabolic Rolementioning
confidence: 99%
“…It is composed of 307 residues, has a Mr of 33,731 calculated from the sequence and is predicted to contain 35% a-helix, 22% P sheet, and 26% reverse turn structures. The proenzyme cleavage site (the amide bond between Ser-81 and Ser-82) is located within a sequence of twenty uncharged residues (positions [69][70][71][72][73][74][75][76][77][78][79][80][81][82][83][84][85][86][87][88] and is predicted to be part of a p-sheet structure that extends from position 71 to position 98. Five of the seven amino acids surrounding the cleavage site from position 78 to ppsition 84 are either serine or threonine residues.…”
Section: Primary Structurementioning
confidence: 99%