2002
DOI: 10.1099/00207713-52-1-263
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Pseudoalteromonas maricaloris sp. nov., isolated from an Australian sponge, and reclassification of [Pseudoalteromonas aurantia] NCIMB 2033 as Pseudoalteromonas flavipulchra sp. nov.

Abstract: A marine, gram-negative, aerobic bacterium that produced cytotoxic, lemon-yellow, chromopeptide pigments that inhibited the development of sea urchin eggs has been isolated from the Australian sponge Fascaplysinopsis reticulata Hentschel. The cells of the organism were rod-shaped with a single polar flagellum and they required NaCl for growth (0.5-10%) with optimum growth at 1-3% NaCl. The temperature for growth was 10-37 degrees C, with optimum growth at 25-30 degrees C. Growth occurred at pH values from 6.0 … Show more

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Cited by 60 publications
(43 citation statements)
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“…The most promising ACC deaminase-producing isolate (# 15) was identified as Pseudoalteromonas maricaloris Ivanova et al (2002). Evaluation of plant growth-promoting activities of WT and NPM strains of P. maricaloris…”
Section: Identification Of Bacteriamentioning
confidence: 99%
“…The most promising ACC deaminase-producing isolate (# 15) was identified as Pseudoalteromonas maricaloris Ivanova et al (2002). Evaluation of plant growth-promoting activities of WT and NPM strains of P. maricaloris…”
Section: Identification Of Bacteriamentioning
confidence: 99%
“…have been isolated from diverse marine habitats globally (13,18,36,49) and are frequently found in association with the surfaces of eukaryotic hosts. Species have been isolated from various animals, such as mussels (23,25), puffer fish (47), tunicates (20), and sponges (26), as well as from a range of marine plants (13,24,56).…”
mentioning
confidence: 99%
“…Antibacterial tests were carried out in duplicate in Petri dishes containing 15 ml of Marine Agar 2216, inoculated with 0.2 ml of a bacterial suspension of H. marina with an OD 520 nm of 0.3 (»2 ÂŁ 10 9 cells/ml). The bacterial suspension was homogeneously swabbed on the agar surface and Wve wells of 6 mm diameter were made on the agar using a sterile Pasteur Pipette [15]. The solutions of extracts were prepared at a concentration of 5% in dimethyl sulfoxide (DMSO, w/v; Sigma).…”
Section: Determination Of Antibacterial Activitymentioning
confidence: 99%