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本文引用的文献

1
Ammonium and Nitrite Inhibition of Methane Oxidation by Methylobacter albus BG8 and Methylosinus trichosporium OB3b at Low Methane Concentrations.在低甲烷浓度下,铵根离子和亚硝酸盐对白色甲基杆菌 BG8 和三孢布拉氏霉菌 OB3b 甲烷氧化的抑制作用。
Appl Environ Microbiol. 1994 Oct;60(10):3508-13. doi: 10.1128/aem.60.10.3508-3513.1994.
2
Methane consumption in temperate and subarctic forest soils: rates, vertical zonation, and responses to water and nitrogen.温带和亚北极森林土壤中的甲烷消耗:速率、垂直分带以及对水和氮的响应。
Appl Environ Microbiol. 1993 Feb;59(2):485-90. doi: 10.1128/aem.59.2.485-490.1993.
3
Effects of Temperature on Methane Consumption in a Forest Soil and in Pure Cultures of the Methanotroph Methylomonas rubra.温度对森林土壤和纯培养甲烷氧化菌甲基单胞菌甲烷消耗的影响。
Appl Environ Microbiol. 1992 Sep;58(9):2758-63. doi: 10.1128/aem.58.9.2758-2763.1992.
4
Rapid methane oxidation in a landfill cover soil.垃圾填埋覆盖土壤中的甲烷快速氧化。
Appl Environ Microbiol. 1990 Nov;56(11):3405-11. doi: 10.1128/aem.56.11.3405-3411.1990.
5
Heterotrophic nitrification in an Acid forest soil and by an Acid-tolerant fungus.酸性森林土壤和耐酸真菌中的异养硝化作用。
Appl Environ Microbiol. 1986 Nov;52(5):1107-11. doi: 10.1128/aem.52.5.1107-1111.1986.
6
Identification of heterotrophic nitrification in a sierran forest soil.在塞拉利昂森林土壤中鉴定异养硝化作用。
Appl Environ Microbiol. 1984 Oct;48(4):802-6. doi: 10.1128/aem.48.4.802-806.1984.
7
Methane Oxidation by Nitrosococcus oceanus and Nitrosomonas europaea.海洋亚硝化球菌和欧洲亚硝化单胞菌的甲烷氧化。
Appl Environ Microbiol. 1983 Feb;45(2):401-10. doi: 10.1128/aem.45.2.401-410.1983.
8
Specific inhibition of nitrite oxidation by chlorate and its use in assessing nitrification in soils and sediments.氯酸盐对亚硝酸盐氧化的特异性抑制及其在评估土壤和沉积物中硝化作用中的应用。
Appl Environ Microbiol. 1980 Mar;39(3):505-10. doi: 10.1128/aem.39.3.505-510.1980.
9
Methane oxidation by Nitrosomonas europaea.欧洲亚硝化单胞菌对甲烷的氧化作用。
Biochem J. 1983 Apr 15;212(1):31-7. doi: 10.1042/bj2120031.
10
Enrichment, isolation and some properties of methane-utilizing bacteria.甲烷利用菌的富集、分离及某些特性
J Gen Microbiol. 1970 May;61(2):205-18. doi: 10.1099/00221287-61-2-205.

机制分析铵对森林土壤中大气甲烷消耗的抑制作用。

Mechanistic analysis of ammonium inhibition of atmospheric methane consumption in forest soils.

机构信息

Darling Marine Center, University of Maine, Walpole, Maine 04573.

出版信息

Appl Environ Microbiol. 1994 Oct;60(10):3514-21. doi: 10.1128/aem.60.10.3514-3521.1994.

DOI:10.1128/aem.60.10.3514-3521.1994
PMID:16349403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC201848/
Abstract

Methane consumption by forest soil was studied in situ and in vitro with respect to responses to nitrogen additions at atmospheric and elevated methane concentrations. Methane concentrations in intact soil decreased continuously from atmospheric levels at the surface to 0.5 ppm at a depth of 14 cm. The consumption rate of atmospheric methane in soils, however, was highest in the 4- to 8-cm depth interval (2.9 nmol per g of dry soil per day), with much lower activities below and above this zone. In contrast, extractable ammonium and nitrate concentrations were highest in the surface layer (0 to 2 cm; 22 and 1.6 mumol per g of dry soil, respectively), as was potential ammonium-oxidizing activity (19 nmol per g of dry soil per day). The difference in zonation between ammonium oxidation and methane consumption suggested that ammonia-oxidizing bacteria did not contribute significantly to atmospheric methane consumption. Exogenous ammonium inhibited methane consumption in situ and in vitro, but the pattern of inhibition did not conform to expectations based on simple competition between ammonia and methane for methane monooxygenase. The extent of ammonium inhibition increased with increasing methane concentration. Inhibition by a single ammonium addition remained constant over a period of 39 days. In addition, nitrite, the end product of methanotrophic ammonia oxidation, was a more effective inhibitor of methane consumption than ammonium. Factors that stimulated ammonium oxidation in soil, e.g., elevated methane concentrations and the availability of cosubstrates such as formate, methanol, or beta-hydroxybutyrate, enhanced ammonium inhibition of methane oxidation, probably as a result of enhanced nitrite production.

摘要

本文研究了大气和升高的甲烷浓度下氮添加对森林土壤甲烷消耗的原位和体外响应。原状土壤中甲烷浓度从表面的大气水平连续下降到 14 厘米深处的 0.5ppm。然而,土壤中大气甲烷的消耗速率在 4 至 8 厘米深度间隔内最高(每天每克干土 2.9 纳摩尔),低于和高于该区域的活性要低得多。相比之下,可提取的铵和硝酸盐浓度在表层(0 至 2 厘米;分别为 22 和 1.6 微摩尔每克干土)最高,潜在的铵氧化活性(每天每克干土 19 纳摩尔)也最高。铵氧化和甲烷消耗的分区差异表明,氨氧化细菌对大气甲烷消耗的贡献不大。外源性铵抑制了原位和体外的甲烷消耗,但抑制模式与基于氨和甲烷对甲烷单加氧酶的简单竞争的预期不符。随着甲烷浓度的增加,铵抑制的程度增加。在 39 天的时间内,单一铵添加的抑制作用保持不变。此外,亚硝酸盐是甲烷氧化氨氧化的终产物,比铵对甲烷消耗的抑制作用更强。土壤中刺激铵氧化的因素,例如,升高的甲烷浓度和作为共底物的甲酸、甲醇或β-羟基丁酸的可用性,增强了铵对甲烷氧化的抑制作用,可能是由于亚硝酸盐产量的增加。