诱导物和金属离子对竹子白腐菌降解影响的研究

研究了4种诱导物和5种金属离子对白腐菌降解竹子的影响。结果表明这4种诱导物对木质素的降解没有明显的促进作用,低浓度的吐温80抑制纤维素的降解,降解率仅为3．057％;5种离子对木质素降解均有促进作用,一定浓度的离子明显地抑制纤维素的降解,其中Ca^2＋对纤维素降解的抑制作用最强,降解率仅为0．620％;诱导物和离子对半纤维素降解率影响较小;吐温80和Ca^2＋能显著提高半纤维素和木质素的选择系数,其中添加Ca^2＋时半纤维素和木质素选择性系数分别为66．565和49．331,初步显示：部分诱导物和金属离子可以有效影响白腐菌对竹子的选择性降解。     

两株丁草胺高效降解菌复配菌剂降解特性研究

LYC-1(Acinetobacter sp.)与LYC-2(Ancylobacter sp.)为两株从长期受农药污染的土壤中分离得到的丁草胺高效降解菌。本研究考察此两株降解菌复配菌剂对丁草胺降解特性,结果表明,菌株LYC-1和LYC-2的菌悬液以3:1的比例混合时,其降解率最高,且高于两个单菌株的降解率。当丁草胺浓度为100 mg·L-1和200 mg·L-1时,混合菌达到最大降解率和生长量,分别为97.8%与1.26(OD600mn)。     

血红密孔菌高产漆酶菌株的筛选及其对烟梗的生物降解

白腐菌是目前已知的唯一能将木质素彻底降解的微生物,而漆酶在木质素分解过程中起着重要的作用,被广泛应用于农作物秸秆或甘蔗渣等多种类型生物质的生物预处理和生物降解。本研究利用白腐菌产漆酶发酵培养基对30株血红密孔菌Pycnoporus sanguineus菌株进行筛选,得到了多株漆酶高产菌株,并研究了血红密孔菌发酵粗酶液和菌丝对烟梗的生物降解条件。研究结果表明:血红密孔菌及其产生的漆酶表现出了对烟梗木质素较强的生物降解能力。在漆酶浓度为40U/mL、温度30℃、pH4.5的条件下处理24h,烟梗中木质素的降解率可达到50.4%,纤维素和半纤维素的降解率分别为17.5%和17.3%;漆酶浓度为5U/mL、温度30℃、pH4.5的条件下处理48h,木质素降解率可达到65.1%。血红密孔菌菌丝也表现出对烟梗较好的生物降解效果,接种培养7d后烟梗中木质素降解率可达30%以上,21d后木质素的降解率可达79.1%,而纤维素和半纤维素的降解率仅为20%和12%左右。本研究不但为生物质材料的生物预处理和生物降解提供了优质的白腐菌及漆酶资源,还为通过烟梗的生物预处理提高烟草梗丝和卷烟品质提供了重要参数,具有一定的应用前景。     

降解菌系和助腐剂对不同还田方式下水稻秸秆降解特征的影响

基于田间小区试验,设置两种秸秆还田处理(以秸秆混土处理模拟旋耕还田,以秸秆不混土处理模拟秸秆沟埋还田),采用尼龙网袋法,通过测定秸秆降解率及秸秆半纤维素、纤维素和木质素的含量,研究两种还田方式下施用降解菌系和助腐剂后水稻秸秆的降解规律。结果表明:在试验前5个月,不混土处理的秸秆降解率始终高于混土处理4.5%～11.6%;至第12个月,混土处理秸秆降解率显著高于不混土处理4.9%～13.0%。在前2个月,各处理水稻秸秆降解较快,秸秆降解率均超过50%,此后秸秆降解进入缓慢期。混土处理中,降解菌系和助腐剂仅能在第1个月提高秸秆的降解效率,此时秸秆降解率分别比对照组高11.0%和10.2%(P0.01);不混土处理中,降解菌系在1～5个月内显著提高秸秆降解效率4.3%～9.7%,助腐剂在1～12个月显著提高秸秆降解效率7.3%～14.4%。试验至第5个月时,喷施助腐剂的秸秆半纤维素、纤维素和木质素的降解率分别达79.1%、80.2%和34.7%,且与喷施菌系处理差异不显著。综上所述,秸秆降解菌系和秸秆助腐剂均能提高水稻秸秆的降解效率,且不混土处理的施用效果好于混土处理。     

白腐菌选择性降解竹基质中木质纤维素的研究

对竹基质白腐菌选择性降解进行了初步研究。结果表明,菌株B1对竹基质中木质素和半纤维素有明显的降解选择性。降解55 d木质素和半纤维素降解率分别达44.4%和47.1%;降解20 d降解选择性最好,木质素和半纤维素降解率选择系数分别是2.08和1.98。从FTIR图谱中木质纤维素相关谱峰(2 924、1 6351、6011、5101、165、1 045、666/cm等)的明显变化也可以得出相同结论。     

耐高温木质素降解菌筛选及降解效果研究

为提高育苗基质中废弃物木质素降解速率,在废弃物堆腐生产育苗基质高温阶段取样,筛选耐高温木质素降解菌,并对菌种进行鉴定,同时测定其对秸秆木质素和菌糠木质素的降解效果。获得了1株较好的木质素高温降解菌HZ11,鉴定为解淀粉芽胞杆菌（Bacillus amyloliquefaciens）,结果显示,该菌株对秸秆木质素和菌糠木质素降解效果较好,50 ℃条件下,20 d木质素降解率分别为46.7%和42.4%。菌株HZ11在降解秸秆和菌糠方面具有很好的应用潜力,为利用农业废弃物生产育苗基质提供更加丰富的菌种资源,具有重要的参考价值。     

N+注入选育白腐菌及其降解油菜秸秆木质纤维素的研究

以白腐菌WY01为出发菌,利用N＋注入技术选育出一株遗传性状稳定的漆酶高产诱变菌株WY02,经过60 d的发酵培养,其产酶量由出发菌的13.75 U/g增加到52.5 U/g,即产酶量提高了2.82倍;诱变菌株WY02对油菜秸秆中的木质素、半纤维素和纤维素的降解率分别为54.1%,39.1%,32.8%,用红外光谱法（IR）分析经诱变菌株降解后的油菜秸秆中木质素官能团的变化,用于阐明诱变菌株对油菜秸秆中木质素的生物降解机制。结果表明：油菜秸秆经白腐菌诱变菌株降解后,其木质素含量明显降低。木质素与苯环相连的C=O键、木质素侧链上CH2结构以及木质素单体（紫丁香基和愈创木基）被部分降解,木质素的苯环结构遭到一定程度的破坏。     

裂褶菌F17固态发酵产锰过氧化物酶及其发酵动力学模型的建立

白腐真菌分泌的锰过氧化物酶是木质素降解酶系统的主要组分,对木质素解聚,纸浆和染料的脱色均有重要作用.利用裂褶菌F17在自行设计的通气托盘式反应器中,以松木屑、稻草及黄豆粉为混合营养基质进行固态发酵生产锰过氧化物酶.在自制通气托盘式反应器中,裂褶菌F17能够产生锰过氧化物酶,发酵96 h时,最高酶活力达到13.51 U/...     

六种白腐菌预处理对毛白杨木材酶水解效果的影响

通过化学分析和酶水解试验,研究了不同的白腐菌对毛白杨的预处理效果及不同组分的降解对酶水解的影响。毛白杨木片经6种白腐菌预处理30d后,各组分都发生了降解,其中半纤维素的损失最为显著,Trametes ochracea C6888引起半纤维素降解率高达47.19%,其次是纤维素和酸不溶木素的降解。在后续酶水解过程中,6种白腐菌处理后的样品显示出不同的水解模式,菌株Trametes ochracea C6888、T. pubescens C7571和T. versicolor C6915预处理效果最为显著,还原糖得率在整个酶水解过程中一直高于对照,其中T. ochracea C6888在水解96h后还原糖得率达到15.93%,比未处理样品提高了25%。分析酸不溶木素降解率及半纤维素降解率与还原糖得率的关系发现,不同菌株在作用同一种基质时,预处理效果差异显著,木质素和半纤维素的脱除都会影响木质纤维素的酶水解。     

多环芳烃降解菌X20的鉴定及降解特性

从多环芳烃降解高效的混合菌群中分离筛选到1株多环芳烃降解菌X20,经形态观察和16SrRNA序列分析,属于假单胞菌(Pseudomonas sp.)。采用室内摇瓶培养的方法,研究了该菌在不同环境条件下对菲和芘的降解。结果表明:弱碱环境有利于菌株X20对菲和芘的降解,最适pH为8.0;葡萄糖对菲芘降解率的影响呈抛物线变化,当葡萄糖浓度为0.2%时,X20对菲和芘的降解达到最高;X20对菲和芘的降解率随其初始浓度的上升而降低,菲和芘在初始浓度为10、20和40mg.L-1时的7d降解率分别为56.3%、39.25%、29.75%和41.8%、29.55%、23.50%,芘对X20降解的抑制强度高于菲。本研究结果将为构建高效的多环芳烃降解菌群,提高多环芳烃原位污染土壤的生物修复效果奠定基础。     

添加剂对水稻秸秆实地混合厌氧发酵产甲烷系统的作用

为提高水稻秸秆利用效率,改进水稻秸秆实地混合厌氧发酵产甲烷技术,本研究开展了添加剂在混合厌氧发酵系统的应用研究。试验选取水稻秸秆和猪粪作为发酵原料,通过分别添加不同的浓度的吐温20和腐植酸,测定甲烷的产气量和浓度、秸秆的降解和土壤肥力的变化,以揭示添加剂类型及其浓度对水稻田实地甲烷生产系统的影响。结果表明:添加剂的掺入并未影响产气的动态变化趋势,但显著地促进产气和提高产气浓度,整体效果由高到低为腐植酸吐温20对照,其中经腐植酸处理的产气量和产气浓度对照相比分别提高了50. 73%和24. 55%。添加剂的掺入有利于水稻秸秆纤维素和半纤维素的降解,但对木质素没有显著影响;其中以0. 15 g/L腐植酸和0. 30 g/L吐温20的降解率最高,相较于对照其纤维素降解率均提高了22. 11%,半纤维素降解率分别提高了107. 13%和98. 39%。添加剂的掺入能显著增加土壤肥力,以0. 15 g/L腐植酸和0. 30 g/L吐温20处理水平的效果最优,相较于对照,其土壤有机质分别增加了29. 63%和23. 72%,全氮分别增加了52. 32%和42. 38%,全磷分别增加了83. 33%和57. 14%。     

高寒森林溪流对凋落叶分解过程中木质素降解的影响

溪流广泛分布于高寒森林地表, 凋落于其中的林木凋落物的分解是整个森林生态系统物质循环的重要环节, 水体流动过程中的冲刷和淋洗作用及其他独特的环境条件可能显著影响凋落物中木质素的降解。该研究采用凋落袋法对比研究了岷江上游高寒森林4种典型且初始质量差异显著的凋落叶, 即康定柳(Salix paraplesia)、高山杜鹃(Rhododendron lapponicum)、方枝柏(Sabina saltuaria)和四川红杉(Larix mastersiana), 在不同生境(林下、溪流和河岸带)下分解过程中木质素残留质量和浓度(质量百分率)的动态变化特征。经过两年的分解, 发现溪流显著促进了凋落叶中木质素的降解; 同一物种凋落叶在不同生境下木质素残留质量差异显著(p < 0.05), 整体表现为溪流<河岸带<林下; 在凋落叶分解的初期木质素有明显的降解, 其浓度表现为先降低后升高, 但不同物种之间存在显著(p < 0.05)的差异; 在整个分解过程中, 木质素残留质量总体呈现出了降低的趋势。此外, 生境类型、分解时期和区域性环境因子(温度、pH值和营养元素的有效性)能显著影响木质素的降解率。这些结果表明, 传统上认为木质素在凋落叶分解初期相对稳定的观点可能并不准确, 其浓度很可能是先下降后升高, 这也与有关木质素动态的最新研究结果相一致。另一方面, 在不同分解时期和不同生境下, 凋落叶木质素降解率表现出了显著差异, 表明区域性环境因子在凋落叶分解和木质素降解过程中具有重要的作用。     

Effects of streams on lignin degradation during foliar litter decomposition in an alpine forest

AimsStreams are widely distributed in alpine forests, and litter decomposition in which is an important component of material cycling across the forest landscape. The leaching and fragmenting effects as well as the unique environmental factors in streams may have significant impacts on lignin degradation during litter decomposition, but studies on this are lacking.
Methods Using litterbag methods, we investigated the dynamics of lignin mass remaining and concentration (percent litter mass, %) during the decomposition of four foliar litters, which varied significantly in the initial litter chemical traits, from the dominant species of Salix paraplesia, Rhododendron lapponicum, Sabina saltuaria, and Larix mastersiana under different habitats (forest floor, stream, and riparian zone) in the upper reaches of the Minjiang River.
Important findings After two year’s incubation, litter lignin mass remaining for a specific litter species varied significantly (p < 0.05) among habitats, with an order of stream < riparian zone < forest floor. Lignin was degraded substantially in the early stage of litter decomposition process, and the lignin concentration first decreased and then increased with the proceeding of litter decomposition, but varied significantly (p < 0.05) among different litter species. Lignin mass showed a general trend of decrease across the 2-year decomposition course. In addition, habitat type, decomposition period and microenvironmental factors (e.g., temperature, pH value and nutrient availability) showed substantial influences on lignin degradation rate. These results suggest that the traditional view that lignin was relatively recalcitrant with an increase of concentration in the early stage of litter decomposition is challenged, but the loss of lignin in the early phrase is in line with recent findings about the fate of lignin during litter decomposition. Moreover, the significant differences of lignin degradation rates among different decomposition period and habitat types indicated that local-scale environmental factors can play a significant role in litter decomposition and lignin degradation processes.     

黄孢原毛平革菌木素过氧化物酶类在天然木素降解中作用的研究

通过诱变得到十一株木素过氧化物酶酶活降低的黄孢原毛平革菌（Ｐｈａｎｅｒｏｃｈａｅｔｅｃｈｒｙｓｏｓｐｏｒｉｕｍ）突变株,用灰色理论分析了其木素过氧化物酶类的产生与木素降解能力间的相关性,并从中筛选到一株木素过氧化物酶缺陷、锰过氧化物酶酶活明显降低的突变株,其木素降解能力为原始菌株的８０％左右。该菌粗酶液作用于纤维素酶酶解杉木木素和天然褐腐木素,可产生小分子的木素降解产物,此反应不需Ｈ２Ｏ２参与。红外光谱分析表明粗酶液对木素的作用主要为氧化作用,因此推测此突变株粗酶液中含有不同于木素过氧化物酶和锰过氧化物酶的与木素氧化降解有关的酶类     

Biodegradation of two tetrameric lignin model compounds by a mixed bacterial culture

Summary The ability of a mixed bacterial culture to decompose two tetrameric lignin model com-pounds as a sole source of carbon and energy was investigated. The mixed bacterial culture con-sisted mainly of Gram negative rods. The tetram-ers contained two types of lignin substructures, namely the most abundant β-O-4 ether structure in lignin and also the 5-5 biphenyl structure. The tetramer (MW 638) containing two phe-nolic hydroxyls was decomposed readily; after 13 days of incubation, all intermediate products formed were almost totally decomposed. The non-phenolic tetramer (MW 666) was decom-posed much more slowly; after 53 days of incuba-tion, 5% of the substrate was unchanged. When both tetramers were degraded simultaneously, the non-phenolic tetramer was decomposed similarly to the phenolic tetramer. Determination of molecular weights of cata-bolic products showed that the degradation of the non-phenolic tetramer had proceeded at least to dimer level. SKF 525A, inhibitor of cytochrome P-450, caused one catabolic product to accumulate in the culture medium. This indicates involvement of cy-tochrome P-450 in the degradation pathway of the model compounds used. We conclude that this mixed bacterial culture was able to degrade the lignin model compounds used and that free phenolic groups seem to in-crease the biodegradability significantly.     

Degradation of non-phenolic lignin by the white-rot fungus Pycnoporus cinnabarinus

High-molecular-weight lignin was methylated with diazomethane. The lignin (i.e., phenolic lignin) and methylated lignin (i.e., non-phenolic lignin) were mixed with fully bleached softwood pulp. Degradation of the lignin preparations by the white rot fungus Pycnoporus cinnabarinus was studied. After a 3-month incubation with the fungus, over 40% of the non-phenolic lignin and about 70% the phenolic lignin were degraded. The presence of phenolic hydroxyl groups in lignin greatly enhanced the degradation rate of lignin. This study reveals that P. cinnabarinus, an exclusively laccase-producing fungus, is capable of oxidatively degrading both phenolic and non-phenolic lignins. The ability of the fungus to degrade non-phenolic lignin suggests that a laccase/mediator system is involved in the complete degradation of lignin. After the fungal degradation of lignins, the content of carboxylic acids substantially increased for both phenolic and non-phenolic lignins.     

Inhibition of the lignin peroxidase of Phanerochaete chrysosporium by hydroxylamino-dinitrotoluene, an early intermediate in the degradation of 2,4,6-trinitrotoluene.

The ability of the white rot fungus Phanerochaete chrysosporium to mineralize 2,4,6-trinitrotoluene (TNT) was studied in the concentration range of 0.36 to 20.36 mg/liter. The initial rate of 14CO2 formation was 30% in 4 days at 0.36 mg of [14C]TNT per liter and decreased to 5% in 4 days at 20.36 mg of [14C]TNT per liter. Such a pronounced inhibition was not observed when a mixture of [14C]2-amino-4,6-dinitrotoluene and [14C]4-amino-2,6-dinitrotoluene was used as a substrate. 2-Hydroxylamino-4,6-dinitrotoluene and its isomer 4-hydroxylamino-2,6-dinitrotoluene were identified as the first detectable degradation products of TNT. Their transient accumulation correlated with the inhibition of TNT degradation and of the veratryl alcohol oxidase activity of lignin peroxidase. With purified lignin peroxidase H8, it could be shown that the two isomers of hydroxylamino-dinitrotoluene were oxidized by lignin peroxidase. The corresponding nitroso-dinitrotoluenes apparently were formed, as indicated by the formation of azoxy-tetranitrotoluenes.     

木质素降解菌的筛选及混合菌发酵降解秸秆的研究

农作物秸秆是农业生产的副产品,也是一项重要的生物资源。由于其成分结构的特殊性所导致的难降解问题,一直成为了转化利用秸秆的难题。目前,利用混合菌将秸秆纤维素转化为蛋白质、乙醇、乙酸、乳酸等研究已逐渐为人们所重视。本文通过马铃薯琼脂平板培养、马铃薯液体摇瓶培养和稻草秸秆固态发酵,从6株常见的食用白腐菌中筛选出了生长优势较强、产漆酶酶活高的平菇HF。为了让秸秆得到更好的降解和利用,采用平菇和康氏木霉二步混合发酵法;通过不同的组合方式,发现H6-T10组合得出的降解效果最好,其木质素降解率达到44.77%,纤维素降解率达到41.48%。