2021
DOI: 10.1016/j.marpolbul.2021.112082
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Fungi in PAH-contaminated marine sediments: Cultivable diversity and tolerance capacity towards PAH

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Cited by 28 publications
(21 citation statements)
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“…Potential carbon sources for fungi in marine sediments that are accessed via exoenzyme secretion include refractory polysaccharides [ 101 ] and refractory carbohydrates (e.g., beta-glucans) [ 102 ]. Fungi take part in degradation of hydrocarbons in soils and sediments, including aromatic compounds [ 103 – 105 ]. Physiologically versatile fungi persist in the deep subsurface biosphere, and have been cultivated from coal-bearing deep subsurface sediments at 2 km depth [ 106 , 107 ].…”
Section: Discussionmentioning
confidence: 99%
“…Potential carbon sources for fungi in marine sediments that are accessed via exoenzyme secretion include refractory polysaccharides [ 101 ] and refractory carbohydrates (e.g., beta-glucans) [ 102 ]. Fungi take part in degradation of hydrocarbons in soils and sediments, including aromatic compounds [ 103 – 105 ]. Physiologically versatile fungi persist in the deep subsurface biosphere, and have been cultivated from coal-bearing deep subsurface sediments at 2 km depth [ 106 , 107 ].…”
Section: Discussionmentioning
confidence: 99%
“…PAHs released into the environment change their state mainly depending on photoconversion or biodegradation [ 31 , 32 ]. Photodegradation is the main pathway for abiotic conversion of most PAHs in the environment [ 33 ].…”
Section: Methodsmentioning
confidence: 99%
“…Initial pH of the medium was adjusted to 7.0-7.2 with sterile 10 M NaOH. Filter sterilized trace element and V7 solutions were added to the sterile MSM as described in previous studies (Kovach et al, 1995;Alvarez-Barragan et al, 2021). The composition of the lysogeny broth (LB) is as follows (g/L): tryptone, 10; yeast extract, 5; NaCl, 10 (Sambrook, 2001).…”
Section: Bacterial Strains and Culture Mediamentioning
confidence: 99%
“…For the microorganisms from the marine samples, MSM (Dias et al, 2008;Alvarez-Barragan et al, 2021) containing 4 g/l sodium acetate as carbon source with 1% agarose was used to fill the wells of the device. The microbial suspension was adjusted to OD 0.1 at 560 nm and diluted 10,000 times before inoculation.…”
Section: Inoculation and Cultivation Of Bacteriamentioning
confidence: 99%