R. Hernández Maqueda, I. Ballesteros, D. Meca, R. Linacero, F. del Moral
{"title":"洞察生态管理温室农业土壤中关键反硝化基因的丰度、表达和多样性","authors":"R. Hernández Maqueda, I. Ballesteros, D. Meca, R. Linacero, F. del Moral","doi":"10.1186/s13765-024-00901-x","DOIUrl":null,"url":null,"abstract":"<div><p>Understanding the bacteria associated with nitrification and denitrification is crucial for comprehending the processes that lead to nitrous oxide emissions in agricultural greenhouse soils. Therefore, it is important to determine their abundance and expression to gain insight into these processes.</p><p>The aim of this study was to explore the bacterial communities associated with denitrification in a greenhouse agricultural soil amended with crop residues and manure for six years. For this purpose, we proceeded to detect and quantify the genes <i>nirK</i> and <i>nirS</i> and the gene <i>nosZ</i> through clone library construction, sequencing, phylogenetic analysis, and quantitative polymerase chain reaction (qPCR). Sequence analysis based on the clone library revealed that many of the <i>nirS</i> or <i>nirK</i> genes detected were not closely related to known denitrifier bacteria, but some of the <i>nosZ</i> sequences were related to the genera such as <i>Pseudomonas</i>, <i>Halomonas</i>, and <i>Marinobacter</i>. Furthermore, the qPCR revealed a high abundance of DNA copies in <i>nirK</i>, 6.08 × 10<sup>9</sup> ± 1.16 × 10<sup>9</sup>, while <i>nirS</i> and <i>nosZ</i> showed lower values, 9.05 × 10<sup>6</sup> ± 1.65 × 10<sup>6</sup> and 8.71 × 10<sup>6</sup> ± 1.44 × 10<sup>6</sup>, respectively. However, the highest expression rate was observed for <i>nirS</i> (mRNA/DNA ratio = 3.10 × 10<sup>− 3</sup>), while <i>nirK</i> and <i>nosZ</i> showed 10-fold lower expression rates (4.4 × 10<sup>− 4</sup> and 3.5 × 10<sup>− 4</sup>, respectively). The results of this work provide a preliminary overview of the diversity, abundance and expression of key genes associated with the denitrification process in this type of soil and are a starting point for further studies to understand how this type of soil management can influence the denitrification process.</p></div>","PeriodicalId":467,"journal":{"name":"Applied Biological Chemistry","volume":"67 1","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2024-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://applbiolchem.springeropen.com/counter/pdf/10.1186/s13765-024-00901-x","citationCount":"0","resultStr":"{\"title\":\"Insights into the abundance, expression and diversity of key denitrification genes in an ecologically managed greenhouse agricultural soil\",\"authors\":\"R. Hernández Maqueda, I. Ballesteros, D. Meca, R. Linacero, F. del Moral\",\"doi\":\"10.1186/s13765-024-00901-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Understanding the bacteria associated with nitrification and denitrification is crucial for comprehending the processes that lead to nitrous oxide emissions in agricultural greenhouse soils. Therefore, it is important to determine their abundance and expression to gain insight into these processes.</p><p>The aim of this study was to explore the bacterial communities associated with denitrification in a greenhouse agricultural soil amended with crop residues and manure for six years. For this purpose, we proceeded to detect and quantify the genes <i>nirK</i> and <i>nirS</i> and the gene <i>nosZ</i> through clone library construction, sequencing, phylogenetic analysis, and quantitative polymerase chain reaction (qPCR). Sequence analysis based on the clone library revealed that many of the <i>nirS</i> or <i>nirK</i> genes detected were not closely related to known denitrifier bacteria, but some of the <i>nosZ</i> sequences were related to the genera such as <i>Pseudomonas</i>, <i>Halomonas</i>, and <i>Marinobacter</i>. Furthermore, the qPCR revealed a high abundance of DNA copies in <i>nirK</i>, 6.08 × 10<sup>9</sup> ± 1.16 × 10<sup>9</sup>, while <i>nirS</i> and <i>nosZ</i> showed lower values, 9.05 × 10<sup>6</sup> ± 1.65 × 10<sup>6</sup> and 8.71 × 10<sup>6</sup> ± 1.44 × 10<sup>6</sup>, respectively. However, the highest expression rate was observed for <i>nirS</i> (mRNA/DNA ratio = 3.10 × 10<sup>− 3</sup>), while <i>nirK</i> and <i>nosZ</i> showed 10-fold lower expression rates (4.4 × 10<sup>− 4</sup> and 3.5 × 10<sup>− 4</sup>, respectively). The results of this work provide a preliminary overview of the diversity, abundance and expression of key genes associated with the denitrification process in this type of soil and are a starting point for further studies to understand how this type of soil management can influence the denitrification process.</p></div>\",\"PeriodicalId\":467,\"journal\":{\"name\":\"Applied Biological Chemistry\",\"volume\":\"67 1\",\"pages\":\"\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-05-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://applbiolchem.springeropen.com/counter/pdf/10.1186/s13765-024-00901-x\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Biological Chemistry\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://link.springer.com/article/10.1186/s13765-024-00901-x\",\"RegionNum\":3,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"FOOD SCIENCE & TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Biological Chemistry","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1186/s13765-024-00901-x","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
Insights into the abundance, expression and diversity of key denitrification genes in an ecologically managed greenhouse agricultural soil
Understanding the bacteria associated with nitrification and denitrification is crucial for comprehending the processes that lead to nitrous oxide emissions in agricultural greenhouse soils. Therefore, it is important to determine their abundance and expression to gain insight into these processes.
The aim of this study was to explore the bacterial communities associated with denitrification in a greenhouse agricultural soil amended with crop residues and manure for six years. For this purpose, we proceeded to detect and quantify the genes nirK and nirS and the gene nosZ through clone library construction, sequencing, phylogenetic analysis, and quantitative polymerase chain reaction (qPCR). Sequence analysis based on the clone library revealed that many of the nirS or nirK genes detected were not closely related to known denitrifier bacteria, but some of the nosZ sequences were related to the genera such as Pseudomonas, Halomonas, and Marinobacter. Furthermore, the qPCR revealed a high abundance of DNA copies in nirK, 6.08 × 109 ± 1.16 × 109, while nirS and nosZ showed lower values, 9.05 × 106 ± 1.65 × 106 and 8.71 × 106 ± 1.44 × 106, respectively. However, the highest expression rate was observed for nirS (mRNA/DNA ratio = 3.10 × 10− 3), while nirK and nosZ showed 10-fold lower expression rates (4.4 × 10− 4 and 3.5 × 10− 4, respectively). The results of this work provide a preliminary overview of the diversity, abundance and expression of key genes associated with the denitrification process in this type of soil and are a starting point for further studies to understand how this type of soil management can influence the denitrification process.
期刊介绍:
Applied Biological Chemistry aims to promote the interchange and dissemination of scientific data among researchers in the field of agricultural and biological chemistry. The journal covers biochemistry and molecular biology, medical and biomaterial science, food science, and environmental science as applied to multidisciplinary agriculture.