草地贪夜蛾幼虫肠道细菌的分离鉴定及纤维素降解细菌的筛选

【目的】本研究旨在明确草地贪夜蛾Spodopterafrugiperda幼虫肠道可培养细菌组成,筛选纤维素降解细菌。【方法】采用传统细菌培养及16S rDNA分子标记相结合的方法分离鉴定草地贪夜蛾幼虫肠道可培养细菌;采用刚果红染色法筛选纤维素降解细菌,并通过3,5-二硝基水杨酸(DNS)法测定不同pH(5.0-9.0)条件下的纤维素酶活力。【结果】从草地贪夜蛾幼虫中筛选分离出14种肠道细菌菌株,分别隶属放线菌门(Actinobacteria)、厚壁菌门(Firmicutes)、变形菌门(Proteobacteria)等3门11属,即谷氨酸棒杆菌属(Glutamicibacter)、肠球菌属(Enterococcus)、芽胞杆菌属(Bacillus)、葡萄球菌属(Staphylococcus)、摩根菌属(Morganella)、肠杆菌属(Enterobacter)、志贺氏菌属(Shigella)、克洛诺杆菌属(Cronobacter)、克雷伯氏菌属(Klebsiella)、沙雷氏菌属(Serratia)、苍白杆菌属(Ochrobactrum)。2株产纤维素酶细菌隶属厚壁菌门芽胞杆菌属。酶活力测定结果显示:2株纤维素降解细菌的纤维素酶在pH 6.0-8.0均有相对较高的活性,在pH 8.0时,纤维素酶活最高。【结论】草地贪夜蛾幼虫肠道中细菌种类多样,其肠道内存在纤维素降解细菌。在偏碱性条件下,纤维素降解细菌的纤维素酶活力显著高于酸性条件。研究结果丰富了纤维素降解细菌资源,在饲料生产、食品加工、化学能源等方面具有应用前景。此外,草地贪夜蛾作为重大农业害虫,其肠道有益菌群,有望成为新的防治靶标。     

阿南原等跳肠道细菌的分离鉴定及降解纤维素细菌的筛选

【目的】本研究旨在确定阿南原等跳Proisotoma ananevae成虫肠道细菌的组成,并筛选降解纤维素细菌。【方法】运用传统培养与16S rDNA测序相结合方法,分离鉴定阿南原等跳成虫肠道内可培养细菌;通过羧甲基纤维素钠筛选培养基(CMC)筛选能够降解纤维素的细菌,并采用3,5-二硝基水杨酸(DNS)法测定不同pH(5.0~9.0)下的纤维素酶活力。【结果】从阿南原等跳成虫肠道共分离到20种不同的菌株,隶属于厚壁菌门(Firmicutes)、变形菌门(Proteobacteria)和放线菌门(Acinobacteria)3门的10属,即葡萄球菌属Staphylococcus,芽孢杆菌属Bacillus,Terribacillus,Advenella,赖氨酸芽孢杆菌属Lysinibacillus,节杆菌属Arthrobacter,肠杆菌属Enterobacter,Glutamicibacter,无色杆菌属Leucobacter和不动杆菌属Acinetobacte;另有1株未鉴别细菌。10株纤维素降解细菌分别隶属于厚壁菌门(Firmicutes)和放线菌门(Acinobacteria)2门的6属,即无色杆菌属Leucobacter,芽孢杆菌属Bacillus,Terribacillus,赖氨酸芽孢杆菌属Lysinibacillus,节杆菌属Arthrobacter和Glutamicibacter。酶活力测定结果显示所有纤维降解素菌株在pH 7.0~9.0之间纤维素酶活性均相对较高,且pH 8.0时酶活力最高。【结论】结果说明,阿南原等跳成虫肠道内存在复杂的细菌结构,在偏碱性条件下降解纤维素的细菌酶活力要高于酸性条件下的酶活力;跳虫作为生态系统中的分解者,其肠道内大量降解纤维素细菌的存在不仅有助于跳虫利用环境中的大分子有机物满足自身的营养等需要,同时对于饲料及工业生产也具有一定的应用价值。     

小龙虾肠道产木聚糖酶细菌的分离与鉴定

【背景】小龙虾肠道微生物是小龙虾降解纤维素和半纤维素的主要驱动力。【目的】研究肠道内细菌的相对丰度,为揭示肠道微生物在小龙虾纤维素降解过程中的作用提供理论支撑。【方法】采用纯培养法从小龙虾肠道筛选产木聚糖酶细菌,并且对小龙虾肠道细菌进行16S高通量测序。【结果】形态学和16SrRNA基因分子鉴定表明,筛选到的4株产木聚糖酶细菌均属于芽孢杆菌科芽孢杆菌属;结合进一步的生理生化特征鉴定,结果为:菌株Z-3为枯草芽孢杆菌(Bacillus subtilis),菌株Z-4为贝莱斯芽孢杆菌(Bacillus velezensis),菌株Z-29为蜡状芽孢杆菌(Bacillus cereus),菌株Z-30为高地芽孢杆菌(Bacillus altitudinis);16S rRNA基因高通量测序结果表明:在属水平上,小龙虾肠道细菌主要是Candidatus Bacilloplasma、拟杆菌属、弧菌属、不动杆菌属、Dysgonomonas、Tyzzerella3、气单胞菌属和希瓦氏菌属细菌。【结论】小龙虾肠道内细菌资源丰富,且芽孢杆菌属细菌在木质纤维素降解过程中发挥一定功能。     

蟋蟀后肠纤维素降解细菌的分离与鉴定

近年来,具有农业、能源和环保价值的昆虫微生物种类和基因得到了开发,昆虫肠道微生物展示了其巨大的应用潜力,本研究旨在从蟋蟀后肠分离和鉴定纤维素降解细菌。首先采用羧甲基纤维素钠液体培养基对蟋蟀后肠中的微生物进行富集培养,然后使用羧甲基纤维素钠固体培养基分离和筛选单菌落,再通过16S rRNA测序对纤维素降解细菌进行分子鉴定,最后通过刚果红染色来进一步分析细菌降解纤维素的能力。从蟋蟀后肠中共分离出20株纤维素降解细菌,16S rRNA基因测序结果显示来自肠杆菌属(Enterobacter)9株,不动杆菌属(Acinetobacter)7株,克雷伯氏菌属(Klebsiella)2株,鞘氨醇杆菌属(Sphingobacterium)1株和葡萄球菌属(Staphylococcus)1株。刚果红染色试验结果显示,克雷伯氏菌属两株PDSCDXS_2B和8B,鞘氨醇杆菌属PDSCDXS_7C和不动杆菌属PDSCDXS_12C具有较高的纤维素降解能力。这是首次从蟋蟀后肠分离和筛选出来具有纤维素降解能力的细菌,为昆虫源纤维素降解细菌的研究提供了微生物资源。     

复合菌系降解纤维素过程中微生物群落结构的变化

为明确高效纤维素降解复合菌系降解过程中微生物群落结构的变化规律及关键的降解功能菌,利用该复合菌系对滤纸和稻秆进行生物处理,通过底物降解、微生物生长量、发酵液pH的变化情况,选择不同降解时期复合菌系提取的总DNA进行细菌16S rRNA基因扩增子高通量测序。通过分解特性试验确定在接种后培养第12、72、168 h分别作为降解初期、高峰期、末期。该复合菌系分别主要由1个门、2个纲、2个目、7个科、11个属组成。随着降解的进行,短芽胞杆菌属Brevibacillus、喜热菌属Caloramator的相对丰度逐渐降低;梭菌属Clostridium、芽胞杆菌属Bacillus、地芽胞杆菌属Geobacillus、柯恩氏菌属Cohnella的相对丰度逐渐升高;解脲芽胞杆菌属Ureibacillus、泰氏菌属Tissierella、刺尾鱼菌属Epulopiscium在降解高峰期时相对丰度最高;各时期类芽胞杆菌属Paenibacillus、瘤胃球菌属Ruminococcus的相对丰度无明显变化。上述11个主要菌属均属于厚壁菌门,具有嗜热、耐热、适应广泛pH、降解纤维素或半纤维素的特性。好氧型细菌是降解初期的主要优势功能菌,到中后期厌氧型细菌逐渐增多,并逐步取代好氧型细菌成为降解纤维素的主要细菌。     

马铃薯块茎蛾肠道细菌分离鉴定及其对植物源大分子化合物的降解作用

为弄清马铃薯块茎蛾肠道可培养细菌的群落结构及其功能。本研究采用牛肉膏蛋白胨培养基,对马铃薯块茎蛾4龄幼虫肠道细菌进行了分离培养,采用16S r DNA序列对各菌株进行种属鉴定,并采用酶鉴定培养基法测定了肠道各细菌对淀粉、纤维素、木聚糖和果胶等植物源大分子物质的降解作用。从马铃薯块茎蛾肠道内共分离到细菌8属10种,分别为不动杆菌属Acinetobacte、葡萄球菌属Staphylococcus、肠杆菌属Enterobacter、节细菌属Arthrobacter、鞘氨醇杆菌属Sphingobacterium、寡养单胞菌属Stenotrophomonas、束村氏菌属Tsukamurella和克雷白氏杆菌属Klebsiella。其中仅鞘氨醇杆菌属菌株LZD10、阿氏节杆菌属菌株LZN13、烟草节杆菌属菌株HZN9对淀粉具有明显的降解作用,但对纤维素、木聚糖和果胶无降解作用,而其余菌株对4种化合物均无降解作用。该研究结果将为深入研究马铃薯块茎蛾对马铃薯块茎的食物适应机制及防治提供理论依据。     

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。     

瘤胃中纤维素分解菌的分离、鉴定及其产酶条件的优化

[目的]从新疆细毛羊、牛和骆驼瘤胃液中分离出具有分解纤维素能力的好氧细菌,用于绿色粗饲料微生物添加剂的研发.[方法]采取新鲜瘤胃液,接种于羧甲基纤维素钠平板,通过刚果红染色和液体复筛培养基,筛选出分解纤维素能力强的好氧细菌;形态学、生理生化试验与16S rDNA序列分析方法相结合对细菌进行鉴定;同时对纤维素分解能力强的4株细菌进行不同条件下酶活力测定.[结果]共分离到84株具有分解纤维素能力的细菌,其中筛选出较强分解纤维素能力的40株.该菌包括37株G-菌和3株G+菌;经鉴定40株纤维素分解菌分别属于6个属10个种,其中16株为寡养单胞菌属,10株为苍白杆菌属,5株为鞘氨醇杆菌属,3株为微杆菌属,3株为副球菌属,2株为假单胞菌属.其中产酶能力强的4株菌在不同条件下的酶活力表明,它们在最佳碳源为秸秆粉、pH5.5-6.0的偏中性条件和37℃培养条件下的酶活力较高.不同菌株对不同纤维素类物质的分解能力不一样,同一菌株对不同纤维素碳源的利用能力也不相同.[结论]分离获得的瘤胃纤维素分解菌是从新疆不同地区、干旱半干旱环境下饲养的动物胃液中分离、筛选出来的,有较强的纤维素分解能力,将为高品质、高消化率的青贮饲料生产提供优质菌种资源及一定的科学依据.     

大莲湖池杉林湿地土壤可培养细菌的分离与鉴定

采用牛肉膏蛋白胨培养基培养,从大莲湖池杉林土壤中共分离得到20个菌落形态不同的菌株。通过对这些菌株的形态、培养特征、生理生化特征的研究以及16S rDNA序列分析,初步确定这些菌株分别属于假单胞菌属(Pseudomonas)、芽胞杆菌属(Bacillus)、红球菌属(Rhodococcus)、北里孢菌属(Kitasatosporia)、金黄杆菌属(Chryseobacterium)、不动杆菌属(Acinetobacter)、黄杆菌属(Flavobacterium)、鞘氨醇杆菌属(Sphingobacte-rium)和丛毛单胞菌属(Comamonas)等9个属细菌。其中芽胞杆菌属和不动杆菌属细菌是优势菌,分离到的红球菌属、北里孢菌属、鞘氨醇杆菌属和丛毛单胞菌属细菌在国内湿地土壤中报道较少。     

番茄潜叶蛾幼虫肠道可培养细菌结构组成及对大分子化合物的降解作用研究

番茄潜叶蛾Tuta absoluta是一种世界毁灭性番茄害虫。为明确其幼虫肠道可培养细菌的多样性及功能,本研究采用LB和NA两种培养基分别对番茄潜叶蛾幼虫肠道细菌组成进行了分离培养,根据细菌菌落形态和16S rDNA序列分析对细菌进行种属鉴定,采用比浊法测定了优势种的生长曲线,并采用透明圈法测定了肠道各可培养细菌对大分子化合物淀粉和纤维素的降解能力。结果表明,从番茄潜叶蛾3龄幼虫肠道中共分离到27株细菌,分属于3门10科17属24种,优势门、科、属、种分别是变形菌门Proteobacteria、欧文氏菌科Erwiniaceae、欧文氏菌属Erwinia、Erwinia iniecta,其相对多度分别达到90.68%、89.41%、89.41%和89.41%。优势种Erwinia iniecta在25℃,180 r/min的条件下培养无迟缓期,0~14 h为对数生长期,14~28 h为稳定期,28 h以后为衰亡期。Glutamicibacter属的L7和L9、考克氏菌属Kocuria的L14和短状杆菌属Brachybacterium的L20能同时降解淀粉和纤维素,考克氏菌属Kocuria的L15和L17只能降解淀粉,欧文氏菌属Erwinia的L、动性球菌属Planococcus的L11、微杆菌属Microbacterium的L18和Prolinoborus属的L22只能降解纤维素,其他菌株无淀粉和纤维素降解能力。综上所述,番茄潜叶蛾幼虫含有24种肠道可培养细菌,种类较为丰富,且部分细菌对淀粉和纤维素大分子化合物具有较强的降解作用,该结果将为番茄潜叶蛾肠道细菌多样性及其功能的深入研究提供依据,同时还为功能细菌的开发利用提供菌株。     

Silicone rubber membrane bioreactors for bacterial cellulose production

Cellulose production byAcetobacter pasteurianus was investigated in static culture using four bioreactors with silicone rubber membrane submerged in the medium. The shape of the membrane was flat sheet, flat sack, tube and cylindrical balloon. Production rate of cellulose as well as its yield on consumed glucose by the bacteria grown on the flat type membranes was approximately ten-fold greater than those on the non-flat ones in spite of the same membrane thickness. The membrane reactor using flat sacks of silicone rubber membrane as support of bacterial pellicle can supply greater ratio of surface to volume than a conventional liquid surface culture and is promising for industrial production of bacterial cellulose in large scale.     

醋酸杆菌发酵生产细菌纤维素的研究进展

简要介绍醋酸杆菌发酵生产纤维素研究进展,内容包括：产纤维素的微生物、醋酸菌纤维素的结构特点、生物合成途径、一般提取处理及分析测定方法、商业用途、工业化发酵生产醋酸菌纤维素过程中存在的主要问题及发展前景。     

Influential factors to enhance the moving rate of Acetobacter xylinum due to its nanofiber secretion on oriented templates

Acetobacter xylinum, a bacterium which secretes a cellulose nanofiber, moves due to the inverse force of extrusion of the fiber, which accordingly correlates with the fiber production rate. To improve the production, the moving rate of the bacterium was focused to examine the influential factors on the substrates for culture and additives in the culture medium. From the real-time video analysis, the oriented template having a strong interaction with the secreted cellulose nanofibers proved to be suitable for the bacteria to move faster. Furthermore, addition of carboxymethylcellulose sodium salt (CMC) to the culture medium cause the bacteria to move faster in the culture medium. In this case, secreted cellulose nanofiber formed different from a normal cellulose nanofiber. The above result could provide an understanding how the formation of cellulose nanofibers contributes to the production rate as well as the bacterial moving rate.     

Characterization of a variant of the polysaccharide acetan produced by a mutant of Acetobacter xylinum strain CR1/4

Acetobacter xylinum NRRL B42 (NCIB 40123) produces both cellulose and a complex anionic branched heteropolysaccharide called acetan. Chemical mutagenesis was used to isolate stable cellulose-minus Acetobacter xylinum mutants. Further chemical mutagenesis of these cellulose-minus A. xylinum bacteria was used to select mutants which secrete polysaccharides which are variants of the acetan structure. Preparation, purification and characterization of these polysaccharides are described. Methylation analysis of the polysaccharide structure CR1/4 suggests that the polysaccharide has an acetan structure with a truncated sidechain terminating in glucuronic acid.     

Utilization of -xylose as carbon source for production of bacterial cellulose

Utilization of -xylose as carbon source for production of bacterial cellulose was studied. Seventeen strains of acetic acid bacteria were screened for their cellulose productivity in -glucose, -xylose, and -xylose/ -xylulose mixed media, respectively. -Xylose was not well metabolized by any bacterial strains that exhibited high cellulose production in -glucose medium. Consequently, bacterial cellulose production in -xylose medium was unsuccessful. -Xylose, however, became utilizable substrate for bacterial strains if xylose-isomerase was added to the medium. Acetobacter xylinus IFO 15606 was the best cellulose producer in -xylose/ -xylulose mixed medium, so cultural conditions were studied for enhanced cellulose production. With pH controlled, the strain could produce cellulose at a yield exceeding 0.3 g per 100 ml of -xylose/ -xylulose mixed medium, which was comparable to the yields in -glucose medium by excellent producers in the literature.     

Surface modification of natural fibers using bacteria: depositing bacterial cellulose onto natural fibers to create hierarchical fiber reinforced nanocomposites

Triggered biodegradable composites made entirely from renewable resources are urgently sought after to improve material recyclability or be able to divert materials from waste streams. Many biobased polymers and natural fibers usually display poor interfacial adhesion when combined in a composite material. Here we propose a way to modify the surfaces of natural fibers by utilizing bacteria ( Acetobacter xylinum) to deposit nanosized bacterial cellulose around natural fibers, which enhances their adhesion to renewable polymers. This paper describes the process of modifying large quantities of natural fibers with bacterial cellulose through their use as substrates for bacteria during fermentation. The modified fibers were characterized by scanning electron microscopy, single fiber tensile tests, X-ray photoelectron spectroscopy, and inverse gas chromatography to determine their surface and mechanical properties. The practical adhesion between the modified fibers and the renewable polymers cellulose acetate butyrate and poly(L-lactic acid) was quantified using the single fiber pullout test.     

Effects of mixing conditions on the production of microbial cellulose byAcetobacter xylinum

Microbial cellulose has many potential applications due to its excellent physical properties. The production of cellulose fromAcetobacter xylinum in submerged culture is, however, beset with numerous problems. The most difficult one has been the appearance of negative mutants under shaking culture conditions, which is deficient of cellulose producing ability. Thus genetic instability ofAcetobacter xylinum under shaking culture condition made developing a stable mutant major research interest in recent years. To find a proper type of bioreactor for the production of microbial cellulose, several production systems were developed. Using a reactor system with planar type impeller with bottom sparging system, it was possible to produce 5 g/L microbial cellulose without generating cellulose minus mutants, which is comparable to that of static culture system.     

The structure of cellulose-producing bacteria, Acetobacter xylinum and Acetobacter acetigenus.

The structure of the pellicles and cells of the cellulose-producing bacteria, Acetobacter xylinum and Acetobacter acetigenus, was studied by transmission electron microscopy of thin sections and freeze-etch replicas of glucose-stimulated cell suspensions, quiescent cell suspensions, and discrete pellicles. These bacteria have a relatively thin cell wall in section, with several irregular features superimposed on an otherwise simple, Gram-negative morphology. There are no flagella or pili. Unfixed, unextracted cells, viewed as whole mounts, show spherical or ellipsoidal bodies of undetermined composition which disappear after extraction with water or ethanol and propylene oxide. For both species, there are several kinds of cell surface irregularities, some of which are localized protrusions of the cell envelope. A variety of irregularities is seen frequently on cells in the first minutes of glucose incubation, on cells in a discrete pellicle, on quiescent cells, and on starved cells. Immediately after the addition of glucose to cellulose-free cells in suspension culture, fine fibrils appear on and (or) near the cell envelope. The fine fibrils are frequently as small as 3 nm in diameter in both freeze-etch and thin-section preparations and are frequently associated with freshly synthesized cellulose fibrils. Starved cells in suspensions free of (classical) microfibrils sometimes reveal stubs of an extracellular structure whose morphology resembles that of a nascent cellulose fibril.