Use of phospholipid fatty acids to detect previous self-heating events in stored peat

The use of the phospholipid fatty acid (PLFA) composition of microorganisms to detect previous self-heating events was studied in naturally self-heated peat and in peat incubated under temperature-controlled conditions. An increased content of total PLFAs was found in self-heated peat compared to th...

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Veröffentlicht in:Applied and Environmental Microbiology 2003-06, Vol.69 (6), p.3532-3539
Hauptverfasser: Ranneklev, S.B, Baath, E
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description The use of the phospholipid fatty acid (PLFA) composition of microorganisms to detect previous self-heating events was studied in naturally self-heated peat and in peat incubated under temperature-controlled conditions. An increased content of total PLFAs was found in self-heated peat compared to that in unheated peat. Two PLFAs, denoted T1 and T2, were detected only in the self-heated peat. Incubation of peat samples at 25 to 55°C for 4 days indicated that T1 and T2 were produced from microorganisms with different optimum temperatures. This was confirmed by isolation of bacteria at 55°C, which produced T2 but not T1. These bacteria produced another PLFA (denoted T3) which coeluted with 18:1omega7. T2 and T3 were identified as omega-cyclohexyltridecanoic acid and omega-cyclohexylundecanoic acid, respectively, indicating that the bacteria belonged to the genus Alicyclobacillus. T1 was tentatively identified as omega-cycloheptylundecanoic acid. T2 was detected 8 h after the peat incubation temperature was increased to 55°C, and maximum levels were found within 5 days of incubation. The PLFA 18:1omega7-T3 increased in proportion to T2. T1 was detected after 96 h at 55°C, and its level increased throughout the incubation period, so that it eventually became one of the dominant PLFAs after 80 days. In peat samples incubated at 55°C and then at 25°C, T1 and T2 disappeared slowly. After 3 months, detectable levels were still found. Incubation at 25°C after heating for 3 days at 55°C decreased the amounts of T2 and 18:1omega7-T3 faster than did incubation at 5°C. Thus, not only the duration and temperature during the heating event but also the storage temperature following heating are important for the detection of PLFAs indicating previous self-heating.
doi_str_mv 10.1128/AEM.69.6.3532-3539.2003
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An increased content of total PLFAs was found in self-heated peat compared to that in unheated peat. Two PLFAs, denoted T1 and T2, were detected only in the self-heated peat. Incubation of peat samples at 25 to 55°C for 4 days indicated that T1 and T2 were produced from microorganisms with different optimum temperatures. This was confirmed by isolation of bacteria at 55°C, which produced T2 but not T1. These bacteria produced another PLFA (denoted T3) which coeluted with 18:1omega7. T2 and T3 were identified as omega-cyclohexyltridecanoic acid and omega-cyclohexylundecanoic acid, respectively, indicating that the bacteria belonged to the genus Alicyclobacillus. T1 was tentatively identified as omega-cycloheptylundecanoic acid. T2 was detected 8 h after the peat incubation temperature was increased to 55°C, and maximum levels were found within 5 days of incubation. The PLFA 18:1omega7-T3 increased in proportion to T2. T1 was detected after 96 h at 55°C, and its level increased throughout the incubation period, so that it eventually became one of the dominant PLFAs after 80 days. In peat samples incubated at 55°C and then at 25°C, T1 and T2 disappeared slowly. After 3 months, detectable levels were still found. Incubation at 25°C after heating for 3 days at 55°C decreased the amounts of T2 and 18:1omega7-T3 faster than did incubation at 5°C. 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Psychology</topic><topic>heat production</topic><topic>Hot Temperature</topic><topic>long chain fatty acids</topic><topic>mesophilic temperature</topic><topic>Microbial Ecology</topic><topic>Microbiology</topic><topic>Mosses</topic><topic>Natural Sciences</topic><topic>Naturvetenskap</topic><topic>peat</topic><topic>peat self heating</topic><topic>phospholipids</topic><topic>Phospholipids - chemistry</topic><topic>Principal Component Analysis</topic><topic>Soil - analysis</topic><topic>Soil Microbiology</topic><topic>species diversity</topic><topic>storage</topic><topic>Temperature</topic><topic>thermophilic bacteria</topic><topic>thermophilic temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ranneklev, S.B</creatorcontrib><creatorcontrib>Baath, E</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SWEPUB Lunds universitet full text</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Lunds universitet</collection><collection>SwePub Articles full text</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ranneklev, S.B</au><au>Baath, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Use of phospholipid fatty acids to detect previous self-heating events in stored peat</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2003-06-01</date><risdate>2003</risdate><volume>69</volume><issue>6</issue><spage>3532</spage><epage>3539</epage><pages>3532-3539</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><coden>AEMIDF</coden><abstract>The use of the phospholipid fatty acid (PLFA) composition of microorganisms to detect previous self-heating events was studied in naturally self-heated peat and in peat incubated under temperature-controlled conditions. An increased content of total PLFAs was found in self-heated peat compared to that in unheated peat. Two PLFAs, denoted T1 and T2, were detected only in the self-heated peat. Incubation of peat samples at 25 to 55°C for 4 days indicated that T1 and T2 were produced from microorganisms with different optimum temperatures. This was confirmed by isolation of bacteria at 55°C, which produced T2 but not T1. These bacteria produced another PLFA (denoted T3) which coeluted with 18:1omega7. T2 and T3 were identified as omega-cyclohexyltridecanoic acid and omega-cyclohexylundecanoic acid, respectively, indicating that the bacteria belonged to the genus Alicyclobacillus. T1 was tentatively identified as omega-cycloheptylundecanoic acid. T2 was detected 8 h after the peat incubation temperature was increased to 55°C, and maximum levels were found within 5 days of incubation. The PLFA 18:1omega7-T3 increased in proportion to T2. T1 was detected after 96 h at 55°C, and its level increased throughout the incubation period, so that it eventually became one of the dominant PLFAs after 80 days. In peat samples incubated at 55°C and then at 25°C, T1 and T2 disappeared slowly. After 3 months, detectable levels were still found. Incubation at 25°C after heating for 3 days at 55°C decreased the amounts of T2 and 18:1omega7-T3 faster than did incubation at 5°C. Thus, not only the duration and temperature during the heating event but also the storage temperature following heating are important for the detection of PLFAs indicating previous self-heating.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>12788760</pmid><doi>10.1128/AEM.69.6.3532-3539.2003</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Alicyclobacillus
Bacteria
Bacteria - chemistry
Bacteria - classification
Biologi
Biological and medical sciences
Biological Sciences
community structure
Culture Media
Ecosystem
fatty acid composition
Fatty acids
Fatty Acids - analysis
Fundamental and applied biological sciences. Psychology
heat production
Hot Temperature
long chain fatty acids
mesophilic temperature
Microbial Ecology
Microbiology
Mosses
Natural Sciences
Naturvetenskap
peat
peat self heating
phospholipids
Phospholipids - chemistry
Principal Component Analysis
Soil - analysis
Soil Microbiology
species diversity
storage
Temperature
thermophilic bacteria
thermophilic temperature
title Use of phospholipid fatty acids to detect previous self-heating events in stored peat
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