典型煤层水微生物产甲烷潜力及其群落结构研究

内蒙古自治区二连盆地、海拉尔盆地是我国重要的煤层气产区,其中生物成因煤层气是煤层气的重要来源,但复杂物质转化产甲烷相关微生物群落结构及功能尚不清楚。【目的】研究煤层水中的微生物代谢挥发性脂肪酸产甲烷的生理特征及群落特征。【方法】以内蒙古自治区二连盆地和海拉尔盆地的四口煤层气井水作为接种物,分别添加乙酸钠、丙酸钠和丁酸钠厌氧培养;定期监测挥发性脂肪酸降解过程中甲烷和底物的变化趋势,应用高通量测序技术,分析原始煤层气井水及稳定期产甲烷菌液的微生物群落结构。【结果】除海拉尔盆地H303煤层气井微生物不能代谢丙酸外,其他样品均具备代谢乙酸、丙酸和丁酸产生甲烷的能力,其生理生态参数存在显著差异,产甲烷延滞期依次是乙酸<丁酸<丙酸;最大比产甲烷速率和底物转化效率依次是丙酸<乙酸<丁酸。富集培养后,古菌群落结构与煤层气井水的来源显著相关,二连盆地优势古菌为氢营养型产甲烷古菌Methanocalculus (相对丰度13.5%–63.4%)和复合营养型产甲烷古菌Methanosarcina (7.9%–51.3%),海拉尔盆地的优势古菌为氢营养型产甲烷古菌Methanobact...     

青藏高原三个盐碱湖的产甲烷菌群和产甲烷代谢途径分析

【目的】分析青藏高原不同类型盐碱湖中的优势产甲烷菌群和优势产甲烷代谢途径。【方法】以不同盐度和植被类型的公珠错、昆仲错和无植被的兹格塘错的沉积物为研究对象,通过高通量测序和q PCR定量古菌16S r RNA多样性分析优势古菌类群;模拟原位盐浓度及p H,比较不同产甲烷底物(甲醇、三甲胺、乙酸和H_2/CO_2)富集沉积物的产甲烷速率,分析其优势产甲烷菌代谢类型。通过添加产甲烷抑制剂(2-溴乙烷磺酸盐),检测沉积物中产甲烷底物积累,确定不同盐碱湖中主要的产甲烷途径。【结果】昆仲错的优势菌群包括甲基/乙酸型的甲烷八叠球菌科(Methanosarcinaceae,11%),乙酸型的甲烷鬃菌科(Methanosaetaceae,7.9%)和氢型甲烷菌甲烷杆菌目(Methanomicrobiales,7.4%);公珠错和兹格塘错的优势菌群为甲烷鬃菌科(Methanosaetaceae)分别占15%和15.3%,及甲烷杆菌属(Methanobacterium)和甲基型的甲烷叶菌属(Methanolobus)。公珠错和昆仲错分别以乙酸和甲醇产甲烷速率最高,而兹格塘错从不同底物产甲烷速率无差异。抑制甲烷产生后,公珠错主要积累乙酸,昆仲错主要积累甲醇;兹格塘错不仅甲烷排放低,也无产甲烷物质显著积累。【结论】昆仲错沉积物中的甲烷主要来自甲醇,公珠错中的甲烷主要来自乙酸,而兹格塘错产甲烷和底物积累不活跃。因而推测高原盐碱湖主要的产甲烷途径和菌群可能与周围植被类型的相关性更高,而与盐度的直接相关性较低。     

温度对甲烷产生和氧化的影响

综述了温度对土壤产甲烷和氧化甲烷的影响及其机制．温度主要通过土壤中产甲烷菌的优势菌发生更替来改变土壤的产甲烷能力．较高温条件下产甲烷菌以乙酸和H2／CO2都能利用的甲烷八叠球菌(Methanosarcinaceae)为主,使得土壤处于较高的产甲烷状态．较低温条件下产甲烷菌以只能利用乙酸的甲烷毛菌(Methanosaetaceae)为主,土壤形成甲烷的能力相对较弱．温度提高可以显著地增加甲烷的产生,Q10为1．5-28,平均4．1,但是温度效应明显受控于底物浓度,提高底物浓度降低了产甲烷菌对底物的亲和力,相应地增加了度效应,因此在较低温条件下提高底物浓度可以促进甲烷的产生．温度对大气甲烷氧化的影响弱于产甲烷,甲烷氧化菌较少受温度变化的影响,即便在较低温条件下,土壤也具有一定的氧化大气甲烷能力,原因尚不清楚,可能与甲烷氧化菌对大气甲烷具有较高的亲和力有关,有待进一步研究．     

寺河矿煤地质产甲烷微生物菌群的保藏和产甲烷性能

【背景】煤地质产甲烷微生物菌群可以代谢煤基质产生甲烷,对于实现煤层气资源的再利用具有重要意义。【目的】检测产甲烷菌群在保藏过程中群落结构的动态变化以及在产气实验中甲烷气的生成情况,以验证保藏方法的可行性,同时为煤层气的微生物增产奠定基础。【方法】分别于不同温度条件下比较3种菌种保藏方法,即甘油/L-半胱氨酸法、富营养法和煤基-基础盐法。通过产气实验检测不同保藏条件下产甲烷菌群的活力。同时,采用454高通量测序技术测定16S r RNA基因序列,分析25°C条件下煤基-基础盐菌种保藏过程中微生物群落结构的变化。【结果】比较了9组菌种保藏方法,发现菌种最佳保藏条件为25°C的煤基-基础盐保藏。在该条件下保藏的产甲烷菌群活性最高,甲烷生成量最大。以无烟煤为碳源进行产气实验时甲烷生成量为12%-25%,而以褐煤为碳源时甲烷生成量可达24%-73%。在25°C的煤基-基础盐菌种保藏条件下,保藏初期细菌的主要优势菌为假单胞菌属(Pseudomonas),而古菌的主要优势菌为甲烷八叠球菌属(Methanosarcina)。随着保藏时间的增加,细菌的群落结构变化显著,发酵细菌及产氢产乙酸细菌成为优势细菌,古菌的群落结构则相对稳定。【结论】菌种保藏的最佳条件为25°C的煤基-基础盐,保藏的产甲烷菌群能长期维持在较高的活性状态,具有较好的产甲烷能力。     

滨海湿地甲烷产生途径和产甲烷菌研究进展

滨海湿地在全球碳循环中起着重要的作用,其甲烷排放量占全球海洋甲烷排放的75%.本文综述了滨海湿地主要甲烷产生途径、产甲烷菌种类及其影响因子.滨海湿地SO₄^2-含量丰富,乙酸发酵和H₂/CO₂途径产甲烷受抑制,乙酸营养型和氢营养型产甲烷菌丰度较低;而利用甲胺类等“非竞争性”底物的C1甲基化合物歧化途径不受硫酸还原菌竞争底物的限制,兼性营养型产甲烷菌成为产甲烷优势菌.盐度与SO₄^2-含量和植被类型密切相关,影响竞争性电子和产甲烷底物的种类和含量,对甲烷产生途径和产甲烷菌群落结构有重要影响.目前,滨海湿地产甲烷菌群落结构、甲烷产生途径的关键控制因素尚需明确,其对甲烷排放的影响有待进一步研究.     

厌氧降解丁酸共培养物中产氢产乙酸细菌与产甲烷细菌的分离与再组合

由处理啤酒厂废水的厌氧消化器颗粒污泥中分离和纯化了一个能厌氧降解丁酸产生甲烷的共培养物BF2。共培养物BF2可降解包括异丁酸在内的含4～18个碳原子的脂肪酸,最适生长温度37℃,最适pH7.7。以巴豆酸为底物,成功地将共培养物BF2分离为专性质子还原产乙酸细菌沃尔夫互营单胞菌嗜脂肪亚种菌株CF2和产甲烷细菌甲酸甲烷杆菌菌株MF2两个纯培养,将它们再组合后仍可降解丁酸。菌株CF2与亨氏甲烷螺菌、布氏甲烷短杆菌菌株1125、甲酸甲烷杆菌菌株1535和普通脱硫弧菌G11组合成人工共培养物,可以厌氧降解丁酸。     

厌氧降解丁酸共培养物中产氢产乙酸细菌与产甲烷细菌的分离与再组合

由处理啤酒厂废水的厌氧消化器颗粒污泥中分离和纯化了一个能厌氧降解丁酸产生甲烷的共培养物BF2。共培养物BF2可降解包括异丁酸在内的含4～18个碳原子的脂肪酸,最适生长温度37℃,最适pH7.7。以巴豆酸为底物,成功地将共培养物BF2分离为专性质子还原产乙酸细菌沃尔夫互营单胞菌嗜脂肪亚种菌株CF2和产甲烷细菌甲酸甲烷杆菌菌株MF2两个纯培养,将它们再组合后仍可降解丁酸。菌株CF2与亨氏甲烷螺菌、布氏甲烷短杆菌菌株1125、甲酸甲烷杆菌菌株1535和普通脱硫弧菌G11组合成人工共培养物,可以厌氧降解丁酸。     

一种产甲烷优势菌群的筛选方法

目的:用简便易行的产甲烷优势菌群的筛选方法,筛选出能够人工培养的且高效产甲烷的复合微生物.方法:用乙酸钠除氧培养基驯化富含产甲烷菌的厌氧活性污泥,逐渐增加驯化体系中培养基和菌液的比率,使驯化体系中微生物菌群适应人工培养条件.结果:筛选出4个产甲烷优势菌群.筛选出的1号、2号、3号、5号菌群在培养7d后均产甲烷量分别达到46mL、38mL、51mL、38mL,在短时间内4个菌群产甲烷量能持续稳定上升.结论:验证表明建立的方法筛选高效产甲烷菌群简便易行,为沼气工作者提供了一定的参考.     

高效降解纤维素产甲烷菌群的富集及其性质研究

以获得1组高效降解纤维素的产甲烷菌群为目的,以蔬菜厌氧消化液、糖蜜厌氧消化液和池塘沉积物底泥为菌株来源,55℃条件下,以滤纸为碳源进行继代培养,检测其甲烷含量,最终获得1组有效分解纤维素的产甲烷菌群。该菌群能够有效分解滤纸,相对分解率可达67.3%,培养7 d甲烷累积产量可达46.5%(体积分数),培养第3天羧甲基纤维素酶(CMC)活性最高值为26.3 U/mL。有机酸中乙酸产量最高,7 d累积量为2.7 g/L。基于16S rRNA基因扩增子高通量测序分析结果表明,细菌的多样性高于古菌。细菌菌群主要由Lutispora、好氧芽胞杆菌属(Aeribacillus)、解硫胺素杆菌属(Aneurinibacillus)、共生小杆菌属(Symbiobacterium)、梭菌属(Clostridium)等组成,其中Lutispora为优势菌群,占细菌总丰度的11.04%。古菌菌群主要包括甲烷嗜热杆菌属(Methanothermobacter)、甲烷丝状菌属(Methanothrix)、甲烷杆菌属(Methanobacterium)、甲烷螺菌(Methanospirillum)等,其中甲烷嗜热杆菌属为优势古菌菌群,占古菌总丰度的99.82%。这组高效降解纤维素的产甲烷菌群可通过多种微生物协同作用实现纤维素的降解和甲烷的产生。     

不同抑制剂对乙酸降解产甲烷及产甲烷菌群结构的影响

摘要:【目的】研究不同温度条件下的石油烃降解产甲烷菌系中是否存在乙酸互营氧化产甲烷代谢途径。【方法】以3个不同温度条件的正十六烷烃降解产甲烷菌系Y15(15℃)、M82(35℃)和SK(55℃)作为接种物,通过乙酸喂养实验、并添加乙酸营养型产甲烷古菌的选择性抑制剂NH4Cl和CH3F,结合末端限制性片段长度多态性(terminal restriction fragment length polymorphism,T-RFLP)和克隆文库技术,分析乙酸产甲烷潜力及产甲烷古菌群落的演替趋势,推测产甲烷代谢途径的变化趋势。【结果】无论是否添加NH4Cl和CH3 F,这3个菌系都可以利用乙酸生长并产生甲烷,但是添加NH4Cl和CH3 F后产甲烷延滞期增加,最大比甲烷增长速率降低;只添加乙酸后,3个不同温度的菌系的古菌群落主要由乙酸营养型产甲烷古菌甲烷鬃毛菌属(Methanosaeta)组成,其丰度分别为92.8±1.4%、97.3±2.4%和82.8±9.0%;当添加选择性抑制剂NH4Cl,3 个菌系中的Methanosaeta的丰度分别变为98.5±0.7%、87.4±4.8%和6.1±8.6%,中温菌系M82中氢营养型产甲烷古菌甲烷袋装菌属(Methanoculleus)的相对丰度增加到12. 6±4.0%,高温菌系SK中另一类氢营养型产甲烷古菌甲烷热杆菌属(Methanothermobacter)增至84.3±1.5%;当添加选择性抑制剂CH3 F,Methanosaeta丰度分别降至77.1 ± 14.5%,86.4±6.1%和35.8±7.8%,低温菌系Y15中的甲烷八叠球菌属(Methanosarcina)增高(15.7±21%),这类产甲烷古菌具有多种产甲烷代谢途径,M82中Methanoculleus丰度上升到13.6±13.1%,SK中Methanothermobacter丰度增大到48.5±11.2%。【结论】在低温条件下,菌系Y15可能主要通过乙酸裂解完成产甲烷代谢,在中高温条件下,菌系M82和SK中可能存在乙酸互营氧化产甲烷代谢途径,并且甲烷的产生分别通过不同种群的氢营养型产甲烷古菌来完成。     

Rapid start-up of thermophilic anaerobic digestion with the turf fraction of MSW as inoculum

This study aims to determine suitable start-up conditions and inoculum sources for thermophilic anaerobic digestion. Within days of incubation MSW at 55 °C, methane was produced at a high rate. In an attempt to narrow down which components of typical MSW contained the thermophilic methanogens, vacuum cleaner dust, banana peel, kitchen waste, and garden waste were tested as inoculum for thermophilic methanogenesis with acetate as the substrate. Results singled out grass turf as the key source of thermophilic acetate degrading methanogenic consortia. Within 4 days of anaerobic incubation (55 °C), anaerobically incubated grass turf samples produced methane accompanied by acetate degradation enabling successful start-up of thermophilic anaerobic digestion. Other essential start-up conditions are specified. Stirring of the culture was not conducive for successful start-up as it resulted specifically in propionate accumulation.     

Characterization of start-up performance and archaeal community shifts during anaerobic self-degradation of waste-activated sludge

Successful start-up strategy for anaerobic digestion of waste-activated sludge using internal inoculum and relationship between the shift of methanogenic community and the digester performance during start-up was investigated. Combination of TS control of inoculum and batch operation during early days enabled the successful start-up operation without serious volatile fatty acid accumulation, followed by the stable continuous operation. However, the propionate degradation was rate-limiting step during the batch operation. The results of real-time quantitative polymerase chain reaction analysis suggested that there was a correlation between the population of the genus Methanosarcina and the methane production rate coupled with acetate consumption during batch operation, and the results of terminal-restriction fragment length polymorphism (T-RFLP) revealed that the increasing intensity of T-RF peaks of hydrogenotrophic methanogens was associated with a decrease in the level of C3-acids.     

Biochemical methane potential (BMP) test for thickened sludge using anaerobic granular sludge at different inoculum/substrate ratios

The biochemical methane potential (BMP) test for thickened sludge was evaluated at three different inoculum/substrate (I:S) ratios. The cumulative methane yield was 51.4 mL CH₄/g VS_added at an I:S ratio of 1:1, 76.3 mL CH₄/g VS_added at an I:S ratio of 1:3, and 21.9 mL CH₄/g VS_added at an I:S ratio of 1:8. The greatest ultimate methane yield and methane production rate constant were achieved at an I:S ratio of 1:3, whereas the least was obtained at an I:S ratio of 1:8. The maximum methane production rate constant was 0.38/day and the minimum methane production rate constant was 0.0016/day. For the case of a lower I:S ratio, the biomass activity may be affected due to the low substrate concentration. On the other hand, for the case of higher I:S ratios, anaerobic digestion of thickened sludge was inhibited by higher concentrations of volatile fatty acids and lower pH.     

The effect of pharmaceuticals on the kinetics of methanogenesis and acetogenesis

In this study, the widely used anaerobic digestion model (ADM1) was used in order to simulate the inhibition of three pharmaceuticals, propranolol hydrochloride, ofloxacin and diclofenac sodium, on two groups of microorganisms, acetogens and acetoclastic methanogens, the most sensitive microorganisms groups involved in the anaerobic digestion process. The specific maximum consumption rate and saturation constant of acetate and propionate degraders were estimated through fitting the model to experimental data taken from continuous and batch experiments. A modified non-competitive inhibition function was used, and the inhibition constants were estimated using data from Batch experiments conducted at various concentrations of pharmaceuticals using enriched cultures with propionate and acetate degraders. It was found that propranolol hydrochloride was the most inhibitory pharmaceutical to both microorganisms groups.     

The effect of enzyme addition on anaerobic digestion of JoseTall Wheat Grass

The effects of the addition of enzyme products containing cellulase, hemicellulase, and β-glucosidase to anaerobic digestion systems were studied using JoseTall Wheat Grass (wheat grass) as a model substrate. Anaerobic digestion tests were performed using batch reactors operated at 50 °C. The application of enzyme products in three digestion configurations were simulated and investigated: (1) enzyme addition to a single-stage digester, (2) pre-treatment of wheat grass with enzymes followed by a single-stage anaerobic digestion, and (3) enzyme addition to the first stage (hydrolysis and acidification) of a two-stage digestion system. The enzyme products showed positive effects on the solubilization of wheat grass when used alone to treat the wheat grass. However, no significant differences in biogas and methane yields, and volatile solids reduction resulted when the enzyme products were tested in the anaerobic digestion systems. This reveals that the microorganisms present in the inoculum were effective in carrying out the digestion of wheat grass. The types of microorganisms present in the inoculum were identified using 16S rRNA sequence analysis. A comparison of the sequences between the different inocula revealed that the prevalent operational taxonomic units were similar, but that the acidified inoculum contained a higher percentage of the species Thermotogae.     

Influence of total solid and inoculum contents on performance of anaerobic reactors treating food waste

The aim of this paper was to analyze the biomethanization process of food waste (FW) from a university campus restaurant in six reactors with three different total solid percentages (20%, 25% and 30% TS) and two different inoculum percentages (20-30% of mesophilic sludge). The experimental procedure was programmed to select the initial performance parameters (total solid and inoculum contents) in a lab-reactor with V: 1100mL and, later, to validate the optimal parameters in a lab-scale batch reactor with V: 5000mL. The best performance for food waste biodegradation and methane generation was the reactor with 20% of total solid and 30% of inoculum: give rise to an acclimation stage with acidogenic/acetogenic activity between 20 and 60 days and methane yield of 0.49L CH4/g VS. Also, lab-scale batch reactor (V: 5000mL) exhibit the classical waste decomposition pattern and the process was completed with high values of methane yield (0.22L CH4/g VS). Finally, a protocol was proposed to enhance the start-up phase for dry thermophilic anaerobic digestion of food waste.     

Microbial Ecophysiology of Whey Biomethanation: Comparison of Carbon Transformation Parameters, Species Composition, and Starter Culture Performance in Continuous Culture

Changes in lactose concentration and feed rate altered bacterial growth and population levels in a whey-processing chemostat. The bacterial population and methane production levels increased in relation to increased lactose concentrations comparable to those in raw whey (6%) and converted over 96% of the substrate to methane, carbon dioxide, and cells. Sequential increases in the chemostat dilution rate demonstrated excellent biomethanation performance at retention times as low as 25 h. Retention times shorter than 25 h caused prevalent bacterial populations and methane production to decrease, and intermediary carbon metabolites accumulated in the following order: acetate, butyrate, propionate, lactate, ethanol, and lactose. Bacterial species dominated in the chemostat as a function of their enhanced substrate uptake and growth kinetic properties. The substrate uptake kinetic properties displayed by the mixed chemostat population were equivalent to those of individual species measured in pure culture, whereas the growth kinetic properties of species in mixed culture were better than those measured in pure culture. A designed starter culture consisting of Leuconostoc mesenteroides, Desulfovibrio vulgaris, Methanosarcina barkeri, and Methanobacterium formicicum displayed biomethanation performance, which was similar to that of a diverse adapted mixed-culture inoculum, in a continuous contact digestor system to which 10 g of dry whey per liter was added. Preserved starter cultures were developed and used as inocula for the start-up of a continuous anaerobic digestion process that was effective for biomethanation of raw whey at a retention time of 100 h.     

Comparison of methane production rate and coenzyme f(420) content of methanogenic consortia in anaerobic granular sludge

The coenzyme F(420) content of granular sludge grown on various substrates and substrate combinations was measured, and the potential of the sludge to form methane (maximum specific methane production rate) from hydrogen, formate, acetate, propionate, and ethanol was determined. The F(420) content varied between 55 nmol g of volatile suspended solids (VSS) for sludge grown on acetate and 796 nmol g of VSS for sludge grown on propionate. The best correlation was found between the F(420) content and the potential activity for methane formation from formate; almost no correlation, however, was found with acetate as the test substrate. The ratio between the potential methanogenic activities (qch(4)) of sludges grown on various substrates and their F(420) content was in general highest for formate (48.2 mumol of CH(4) mumol of F(420) min) and lowest for propionate (6.9 mumol of CH(4) mumol of F(420) min) as test substrates. However, acetate-grown granular sludge with acetate as test substrate showed the highest ratio, namely, 229 mumol of CH(4) mumol of F(420) min. The data presented indicate that the F(420) content of methanogenic consortia can be misleading for the assessment of their potential acetoclastic methanogenic activity.     

Characterization of food waste as feedstock for anaerobic digestion

Food waste collected in the City of San Francisco, California, was characterized for its potential for use as a feedstock for anaerobic digestion processes. The daily and weekly variations of food waste composition over a two-month period were measured. The anaerobic digestibility and biogas and methane yields of the food waste were evaluated using batch anaerobic digestion tests performed at 50 degrees C. The daily average moisture content (MC) and the ratio of volatile solids to total solids (VS/TS) determined from a week-long sampling were 70% and 83%, respectively, while the weekly average MC and VS/TS were 74% and 87%, respectively. The nutrient content analysis showed that the food waste contained well balanced nutrients for anaerobic microorganisms. The methane yield was determined to be 348 and 435 mL/gVS, respectively, after 10 and 28 days of digestion. The average methane content of biogas was 73%. The average VS destruction was 81% at the end of the 28-day digestion test. The results of this study indicate that the food waste is a highly desirable substrate for anaerobic digesters with regards to its high biodegradability and methane yield.     

The effect of incubation conditions on the laboratory measurement of the methane producing capacity of livestock wastes

The effects of incubations conditions (dilution, mixing, incubation time and inoculum amount and origin) on the determination of the maximum methane producing capacity (B(0)) from various livestock slurries were evaluated. For this purpose, the methane yields of different livestock slurries were determined using batch anaerobic incubations performed at 30 degrees C as regard these different conditions. The B(0) and the methane (CH(4)) generation as a function of time were used to study the processes and to determine the best incubation conditions. Methanogenesis was identified as the major rate-limiting step during the anaerobic degradation of slurries, probably due to inhibition by volatile fatty acids. In some cases, high free NH(3) concentrations were suspected to inhibit the hydrolysis process. The addition of inoculum and/or the dilution of the substrate reduced the inhibition and allowed to reach the B(0) more rapidly. However, the addition of inoculum must be minimized to reduce the possible errors made by considering a similar production by the inoculum with and without the substrate. All experiments performed during this study allowed to define the incubation conditions required for the determination of the B(0) from livestock slurries. Applying these conditions, the B(0) values determined for swine slurries varied from 244 to 343L CH(4)kg V(added)(-1), from 204 to 296L CH(4)kg V(added)(-1) for dairy cattle slurries and equalled 386 and 319L CH(4)kg VS(added)(-1) respectively for calves and duck slurries.