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Use of Phospholipid Fatty Acids To Detect Previous Self-Heating Events in Stored Peat

机译:使用磷脂脂肪酸检测存储的泥炭中以前的自热事件

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摘要

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 18:1ω7. T2 and T3 were identified as ω-cyclohexyltridecanoic acid and ω-cyclohexylundecanoic acid, respectively, indicating that the bacteria belonged to the genus Alicyclobacillus. T1 was tentatively identified as ω-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 18:1ω7-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 18:1ω7-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.
机译:在自然自热的泥炭中和在温度受控条件下孵育的泥炭中,研究了使用磷脂脂肪酸(PLFA)微生物组成检测先前的自热事件。与未加热的泥炭相比,发现自加热泥炭中总PLFA含量增加。仅在自加热的泥炭中检测到两个PLFA,分别表示为T1和T2。泥炭样品在25至55°C下孵育4天表明T1和T2是由具有不同最佳温度的微生物产生的。通过在55°C分离细菌可证实这一点,该细菌可产生T2而不产生T1。这些细菌产生另一种PLFA(称为T3),与18:1ω7共洗脱。 T2和T3分别被鉴定为ω-环己基十三烷酸和ω-环己基十一烷酸,表明该细菌属于脂环芽孢杆菌属。暂时将T1鉴定为ω-环庚基十一烷酸。将泥炭培养温度升至55°C 8小时后检测到T2,在培养5天之内发现了最高水平。 PLFA 18:1ω7-T3与T2成比例增加。在55°C下96小时后检测到T1,并且在整个孵育过程中T1的水平均升高,因此在80天后它最终成为占主导地位的PLFA之一。在55°C,然后在25°C孵育的泥炭样品中,T1和T2缓慢消失。 3个月后,仍发现可检测的水平。在55°C下加热3天后,在25°C下孵育比在5°C下孵育更快地降低了T2和18:1ω7-T3的含量。因此,对于加热指示之前的自加热的PLFA,不仅加热事件期间的持续时间和温度而且加热之后的储存温度也很重要。

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