南海东海岛沉积物分离细菌的鉴定及其抑菌活性

[背景] 海洋微生物在活性物质开发方面具有巨大的应用前景,而目前有关南海东海岛微生物的研究鲜少。[方法] 对从东海岛沉积物中分离纯化的海洋细菌,采用形态学观察、生理生化以及16S rRNA基因序列的系统发育分析方法进行鉴定;以大肠杆菌（Escherichia coli）、枯草芽孢杆菌（Bacillus subtilis）和金黄色葡萄球菌（Staphylococcus aureus）作为指示菌,测定其抑菌活性;对具有抑菌活性的菌株扩增聚酮合酶（Polyketide synthase I,PKSI）基因,并与已知的PKSI氨基酸序列比对;选择具有PKSI基因的代表菌株,检测菌株及其发酵抑菌物的稳定性。[结果] 分离纯化到25株海洋细菌,分属于不动杆菌属（Acinetobacter）、交替单胞菌属（Alteromonas）、芽孢杆菌属（Bacillus）、嗜冷杆菌属（Psychrobacter）、假交替单胞菌属（Pseudo-alteromonas）、海洋单胞菌属（Oceanimonas）、葡萄球菌属（Staphylococcus）、微球菌属（Micrococcus）和海杆菌属（Marinobacter）。12株菌株通过基因筛选检测到PKSI编码基因,其中6株菌株具有抑菌活性和PKSI编码基因,并分属于芽孢杆菌属和交替单胞菌属;PKSI氨基酸序列同源性分析推测菌株DHD-15和DHD-a可能产生新的I型聚酮合酶结构。菌株DHD-15和DHD-L生长温度范围为15-40℃,可耐受10% NaCl高盐以及pH 3和pH 11的酸碱条件,但不耐高温;菌株DHD-15产生的抑菌物质可耐受100℃和pH 11的高温碱性条件,在50℃、pH 9条件下制备和室温保藏条件下抑菌活性较高,其稳定性较好。[结论] 南海东海岛沉积物筛选的细菌种具有抑菌活性,具有产聚酮类活性物质的潜力。     

漳江口红树林沉积物可培养真菌多样性

红树林真菌由于其独特的生态特征、多样性特点和丰富的新型生物活性代谢产物而引起了广泛的关注。本文以漳江口红树林保护区4个采样点的沉积物为研究对象，采用8种筛选培养基（RBM、PDA、CDA、Martin、YM、SDA、ISP2和R2A）分离可培养真菌，根据ITS序列分析对其进行物种鉴定，并利用多样性指数分析评价不同采样点真菌群落的差异。结果共分离到274株真菌，隶属于2门12纲23目39科52属，其中优势属为枝顶孢属（Acremonium）（20.8%）和青霉属（Penicillium）（11.3%），其次是枝孢属（Cladosporium）（7.3%）和帚枝霉属（Sarocladium）（7.3%）。8种筛选培养基中，分离出真菌种属类型最丰富的培养基是RBM，其次是PDA。根据Shannon-Wiener多样性指数（H′）、Simpson优势度指数（D）、Magalef丰富度指数（R）和Pielou均匀度指数（J）的分析结果，在属的水平上，距海洋的位置越近，真菌的群落多样性越高，真菌分布越均匀。     

云南嵩明大哨天然虫生真菌及其内生真菌的分离鉴定与抑菌活性分析

【背景】云南存在着丰富的虫草资源,天然虫草群落中蕴藏多样的真菌资源,是挖掘新型抑菌活性化合物的潜在来源。【目的】了解云南嵩明大哨天然虫生真菌及其内生真菌的物种多样性,并从中筛选具有抑菌活性的菌株。【方法】采用组织分离法对所采集的野生虫草样本进行虫生真菌及其内生真菌的分离,并通过形态观察和ITS联合nrSSU、nrLSU、tef-1α、rpb1、rpb2多基因测序进行物种鉴定及多样性分析;通过平板对峙法以7株病原细菌、5株植物病原真菌为病原指示菌进行抑菌活性测试。【结果】共采集86份天然虫草样本,经鉴定隶属于3科5属7种,包括虫草科（Cordycipitaceae）虫草属（Cordyceps）（1种）、白僵菌属（Beauveria）（2种）、鳞翅虫草属（Samsoniella）（2种）、麦角菌科（Clavicipitaceae）泛普可尼亚属（Metapochonia）（1种）,以及线虫草科（Ophiocordycipitaceae）线虫草属（Ophiocordyceps）（1种）。同时,从采集到的虫草样本中分离得到26株内生真菌,分属于9科9属,其中木霉属（Trichoderma）（38%）和镰刀菌属（Fusarium）（19%）为此次分离得到的优势菌属。对所分离保存的真菌按其分离源及种类归属,从虫生真菌和内生真菌菌株中共挑取20株代表性菌株进行抑菌活性筛选,有11株真菌对2株及以上病原指示细菌具有不同程度的抑菌活性,13株真菌对1株以上植物病原真菌具有不同程度拮抗能力;其中Trichoderma sp.Y3-1和Fusarium sp.WZ3-1具有广谱抑菌活性。【结论】云南嵩明大哨分布有丰富的虫生真菌及内生真菌资源,分离所得的真菌对多种病原菌具有不同程度的抑制作用。本研究丰富了云南虫草资源多样性,为云南省虫草及其内生真菌资源的开发利用提供了数据支持,也为下一步从虫草及其相关真菌资源中挖掘抑菌活性物质提供了菌株资源。     

三种松树内生真菌的分离鉴定及其对红脂大小蠹伴生真菌的拮抗作用

【背景】松树的内生真菌会影响红脂大小蠹及其伴生真菌的生长及扩散,从而影响红脂大小蠹的入侵。【目的】掌握赤峰地区红脂大小蠹寄主树种内生真菌的物种多样性,筛选对其伴生菌有拮抗作用的菌株,为红脂大小蠹的生物防治提供资源。【方法】采用组织分离法、形态学鉴定和internal transcribed spacer (ITS)序列分析相结合的方法对红脂大小蠹寄主树种油松、樟子松和潜在寄主落叶松进行内生真菌多样性研究,并用两点对峙法进行拮抗菌株筛选。【结果】松树内生真菌鉴定为2门6纲10目18科19属,其中落叶松韧皮部分离到的内生真菌数量最多,为39株,隶属于9属12种,真菌检出率为43.33%;油松次之,为30株,隶属于7属8种,真菌检出率为33.33%;樟子松最少,为29株,隶属于10属13种,真菌检出率为32.22%。3个树种的内生真菌相似性较低,无共有的菌种,青霉属(Penicillium)和篮状菌属(Talaromyces)是唯二的共有菌属,且青霉属在3个树种中均为优势菌属。平板对峙结果表明90%以上的树木内生真菌均能够与伴生真菌形成稳定的对峙,抑制率在50%-86%之间,且Phialocephala sp.和Pochonia bulbillosa对伴生菌的抑制率能高达93.7%。【结论】松树韧皮部的内生真菌具有较高的生防潜力,Phialocephala sp.和P. bulbillosa对红脂大小蠹伴生菌有较好的抑制效果,可作为红脂大小蠹的生防资源。     

不同分布区胀果甘草原生境土壤微生物群落结构特征及其影响因素

胀果甘草（Glycyrrhiza inflata）主要分布于新疆、甘肃的荒漠区,是耐盐性最强的药用甘草,在改良盐碱地土壤中发挥着重要作用,其原生境土壤微生物群落结构特征是揭示种群分布影响因素及盐碱地修复机制的重要依据。从胀果甘草5个主产区采集原生境土壤,测定土壤理化指标,并采用高通量测序技术,结合Spearman、dbRDA等方法开展微生物群落组成及多样性特征研究,揭示不同分布区的优势微生物群落特征和影响因子。结果表明：真菌群落中曲霉属（Aspergillus）、地丝霉属（Geomyces）、镰刀菌属（Fusarium）和细菌群落中的寡养单胞菌属（Stenotrophomonas）、Marinimicrobium、Idiomarina是野生胀果甘草原生境土壤中的优势微生物类群。不同分布区的土壤真菌多样性和丰富度具有显著差异,但土壤细菌多样性和丰富度差异不显著;部分分布区土壤中的真菌和细菌种类差异较大。土壤理化因子中,土壤含水量和总含盐量对真菌和细菌的群落分布、丰富度有显著影响。原生境含水量与曲霉属（Aspergillus）、镰刀菌属（Fusarium）、链格孢属（Alternaria）、青霉属（Penicillium）真菌呈显著负相关;与Marinnimicrobium,Idiomarina、Aliifodinibius和需盐杆菌属（Salegentibacter）细菌呈显著正相关,与链霉菌属（Streptomyces）细菌呈显著负相关。原生境土壤总含盐量,与曲霉属（Aspergillus）、裸子囊菌属（Gymnoascus）、Aporospora真菌呈显著正相关,与镰刀菌属（Fusarium）、丝盖伞属（Inocybe）、硬皮马勃属（Scleroderma）真菌呈显著负相关;总盐含量与Marinimicrobium、Idiomarina、嗜盐单胞菌属（Halomonas）、Aliifodinibius、Salinimicrobium、需盐杆菌属（Salegentibacter）这6种细菌的丰富度存在显著正相关关系,与链霉菌属（Streptomyces）和鞘氨醇单胞菌属（Sphingomonas）细菌呈显著负相关。另外,土壤真菌和细菌的空间分布的异质性也与野生胀果甘草的生境类型和地理环境有关。原生境中丰富度高的嗜盐细菌可能与胀果甘草的盐适应和耐盐机制有密切关系。研究结果为野生胀果甘草的种群恢复、盐碱弃耕地的土壤功能修复研究提供理论依据。     

古树大理茶优势内生真菌1个新四氢-β-咔啉二酮哌嗪的分离鉴定

为挖掘古树大理茶优势内生真菌间座壳属菌株Diaporthe tectonigena的化学成分,该研究采用硅胶、大孔吸附树脂Diaion HP20、葡聚糖凝胶LH-20等柱层析方法,对该菌株的大米固态发酵提取物进行分离纯化,并通过HRMS、¹H-NMR、¹³C-NMR、HSQC、HMBC和COSY等波谱分析,对所得化合物进行结构鉴定。结果表明:(1)从该菌株大米固态发酵提取物中分离得到4个化合物,其中新化合物1鉴定为四氢-β-咔啉二酮哌嗪类生物碱,命名为tectonicgenazine A。(2)3个已知化合物分别鉴定为trans-cyclo-(D-tryptophanyl-L-tyrosyl)(2)、1H-吲哚-3-羧酸-2,3-二羟基丙酯(3)和N-羟乙基-2-乙酰基吡咯(4),其中化合物3为首次从自然界中分离所得。     

烟草根际可培养微生物多样性及防病促生菌的筛选

[背景] 根际微生物在植物根部生态系统中扮演着重要角色,影响着植物的营养吸收和健康生长。[目的] 了解常年不发病烟田烤烟品种K326根际可培养微生物的多样性,筛选具有防病促生功能的菌株,为烟草病害绿色防控提供资源。[方法] 采用传统培养方法对烟草根际土壤中的细菌和真菌进行分离鉴定,评价菌株的促生特性及病原菌拮抗能力,并进一步验证典型菌株对盆栽烟苗的促生效果。[结果] 共获得261株微生物菌株,包括160株细菌和101株真菌。经分子鉴定,细菌中以变形菌门（Proteobacteria）和厚壁菌门（Firmicutes）为主要类群;真菌中以子囊菌门（Ascomycota）和毛霉菌门（Mucoromycota）为主要类群。在属水平上,细菌以假单胞菌属（Pseudomonas）和芽孢杆菌属（Bacillus）为主,真菌以曲霉属（Aspergillus）和青霉属（Penicillium）为主。从不同种水平上进一步选择44株细菌为代表菌株,发现它们均具有不同程度的吲哚-3-乙酸（Indole-3-Acetic Acid,IAA）产生能力,9株能够溶解有机磷,16株能够溶解无机磷,13株产生铁载体,14株产生生1-氨基环丙烷-1-羧酸（1-Aminocyclopropane-1-Carboxylate,ACC）脱氨酶。从160株细菌中筛选得到抑制青枯病菌和黑胫病菌的菌株数目分别为25、26株。经盆栽试验发现韩国假单胞菌（P. koreensis） HCH2-3、浅黄绿假单胞菌（P. lurida） FGD5-2和贝莱斯芽孢杆菌（B. velezensis） EM-1对烟苗呈现不同程度的促生作用,其中3株菌联合施加对烟苗的促生效果最明显。[结论] 烟草根际存在着丰富多样的具有防病促生潜力的微生物,并且合成菌群或功能互补的菌株联合施用是未来微生物菌剂研发的重要方向。     

云南三个地区马铃薯内生真菌多样性研究

为研究云南马铃薯(Solanum tuberosum)内生真菌的多样性,该文以采自云南省德宏芒市、大理喜洲和临沧双江3个地区的马铃薯植株为研究对象,采用组织块分离法、尖端菌丝挑取法对马铃薯根、茎及块茎中的内生真菌进行分离纯化,并采用形态学鉴定方法和ITS序列分析法对分离得到的内生真菌进行鉴定,对内生真菌的定殖率、分离率及多样性指数进行计算和分析。结果表明:(1)共分离得到内生真菌98株,其中从德宏芒市的样品中获得40株,从大理喜洲的样品中获得27株,从临沧双江的样品中获得31株。(2)经鉴定,分离得到的马铃薯内生真菌共涵盖10目10科13属,大多为子囊菌门和担子菌门,优势菌为镰刀菌属(Fusarium)和青霉属(Penicillium),褶皱裸孢壳(Emericella rugulosa)、接骨木镰刀菌(Fusarium sambucinum)、毛韧革菌(Stereum hirsutum)、Psathyrella sulcatotuberculosa和Epicoccum catenisporum 5种真菌均为首次从马铃薯植株中分离得到。(3)马铃薯块茎内生真菌的定殖率最高,根部内生真菌定殖率最低; 内生真菌的分离率以马铃薯根部为最高,而茎部最低; 不同组织中内生真菌的多样性指数趋势均为根>块茎>茎。从综合来看,云南马铃薯植株中的内生真菌具有较高的多样性,不同地区的马铃薯样品中内生真菌优势菌不同,马铃薯根部具有最丰富的内生真菌种群和最高的分离率,是最适合进行内生真菌分离的材料。该研究结果为后期探究马铃薯内生真菌对病原菌的拮抗作用奠定了基础,也为马铃薯内生真菌多样性研究提供了参考数据。     

夏季故宫养心殿空气中真菌的调查与分析

【目的】在无法实现洁净环境的古建筑内,文物易遭受霉菌的破坏,尤其是在闷热的夏季。探明空气中真菌的种类对文物、游客的安全具有重要意义。【方法】采用自然沉降法与撞击法对夏季养心殿正殿内代表性的6个取样位置的气生真菌进行培养并进行ITS1 rDNA序列分析。【结果】利用自然沉降法测得气生真菌22种,以枝孢属(Cladosporium)、曲霉属(Aspergillus)和青霉属(Penicillium)为优势类群,在2个位置(佛堂二层与西暖阁)空气真菌污染超标;而撞击法测得100余种,腐生营养型真菌比例较高,优势类群为链格孢属(Alternaria)、Cladosporium、木霉属 (Trichoderma)、根霉属(Rhizopus)、Aspergillus和Penicillium,所有6个位置均超标。通过对环境因子与真菌多样性的相关性分析发现,养心殿内真菌丰度与温度、湿度及悬浮颗粒物有着密切关系。在相对湿度较低的6月,温度对丰度影响较大;高湿度时,悬浮颗粒物与湿度对真菌丰度影响更大。丝状真菌的丰度与小粒径悬浮颗粒物、相对湿度存在显著正相关,而空气中的酵母菌与温度相关性更高。【结论】本研究对养心殿正殿空气中真菌的种属进行了鉴定,并分析了与环境因子的相关性,为预防、开放展览以及修缮提供了科学依据。     

利用含油培养基富集、分离和评估海洋产聚羟基脂肪酸酯细菌

[背景] 细菌可通过脂肪酸代谢途径耦合聚羟基脂肪酸酯（Polyhydroxyalkanoate,PHA）合成途径实现合成中长链PHA;其拉伸强度、玻璃化温度等加工特性均优于短链PHA,是未来工业化PHA材料的发展方向。[目标] 为了获得新的可代谢油类的产PHA细菌,使用3种分离策略从海洋沉积物中分离和鉴定细菌,并评估菌株产PHA的能力。[方法] 采集深圳大鹏湾近海沉积物样品;样品通过直接分离,5周连续培养分离,或10周连续提高盐度（3.5%-12.5%）和含油量（1%-10%）富集培养分离,纯化得到菌株;通过16S rRNA基因相似性及系统进化分析鉴定细菌分类地位,利用PHA聚合酶（PhaC）基因鉴定细菌合成PHA的能力;通过测定基因组框架图,分析细菌的PhaC类型、代谢通路及系统进化关系;通过气相色谱分析细菌产PHA的含量及组成。[结果] 从深圳大鹏湾近海底泥样品中分离得到96株细菌,phaC基因阳性率达38%,其中包含9个此前未通过产物证实可产PHA的属,包括尖球菌属（Acuticoccus）、海洋源菌属（Idiomarina）、盐芽孢杆菌属（Halobacillus）、微泡菌属（Microbulbifer）、海棍状菌属（Maritimibacter）、硝酸盐还原菌属（Nitratireductor）、公海橄榄菌属（Pelagibaca）、假海栖菌属（Pseudooceanicola）和海旋菌属（Thalassospira）。除了微泡菌属,其他8个属的细菌通过含油富集法分离获得,说明含油富集方法有利于发现新的产PHA细菌资源。此外,获得2株胞内PHA含量高的菌株。Nitratireductor aquimarinus SY-2-4在营养肉汤中培养可累积细胞干重35.0%的PHA;Roseibium aggregate SN13-21以丙酮酸盐为碳源,可累积细胞干重19.9%的PHA。[结论] 大鹏海域蕴藏着丰富的产PHA细菌资源,值得进一步挖掘研究。梯度增加含油量和盐度的富集方法有利于分离区系不同的产PHA细菌,适用于分离PHA资源。获得2株潜在PHA高产菌,未来将对菌株进行发酵优化研究。     

Isolation and Characterization of Antifungal Substances from Burkholderia sp. Culture Broth

A new antagonistic Burkholderia strain, designated MP-1 and producing antifungal activities against various filamentous plant pathogenic fungi, was isolated from the rhizoshere in the Naju area. Cultural characteristic studies strongly suggested that this strain belongs to the genus Burkholderia. The nucleotide sequence of the 16S rRNA gene (1491 pb) of strain MP-1 exhibited close similarity (99% to 100%) with other Burkholderia 16S rRNA genes. Extraction of fermentation broth of Burkholderia sp. MP-1 and various separations and purification steps led to isolation of four pure active molecules. The chemical structure of these four compounds—named phenylacetic acid, hydrocinnamic acid, 4-hydroxyphenylacetic acid, and 4-hydroxyphenylacetate methyl ester—was established on the basis on their gas chromatography–electron impact–mass spectrometry (GC-EI-MS) and trimethylsilation GC-EI-MS data. The four isolated compounds inhibited filamentous fungal growth on potato dextrose agar medium supplemented with 100 mg/L of phenylacetic acid, hydrocinnamic acid, 4-hydroxyphenylacetic acid and 4-hydroxyphenylacetate methyl ester individually.     

青霉单宁酶高活性菌株的诱变选育

利用塔拉单宁诱导丝状真菌产生单宁酶的原理,通过富集培养,从天然源分离得到30株具有较高单宁酶活性的青霉菌;经二级发酵程序,对这30株菌进行了生物转化复筛实验,选择出能水解塔拉单宁,且生物催化活性较高的青霉野生株Penicilliumsp.No.23,对No.23进行经紫外诱变处理,诱变株经筛选,最后得到1株具有稳定遗传性的单宁酶高活性菌株,其单宁酶活性比出发菌株提高了35%。     

Production of tannase from Aspergillus ruber under solid-state fermentation using jamun (Syzygium cumini) leaves

Tannase producing fungal strains were isolated from different locations including garbages, forests and orchards, etc. The strain giving maximum enzyme yield was identified to be Aspergillus ruber. Enzyme production was studied under solid state fermentation using different tannin rich substrates like ber leaves (Zyzyphus mauritiana), jamun leaves (Syzygium cumini), amla leaves (Phyllanthus emblica) and jawar leaves (Sorghum vulgaris). Jamun leaves were found to be the best substrate for enzyme production under solid-state fermentation (SSF). In SSF with jamun leaves, the maximum production of tannase was found to be at 30 °C after 96 h of incubation. Tap water was found to be the best moistening agent, with pH 5.5 in ratio of 1:2 (w/v) with substrate. Addition of carbon and nitrogen sources to the medium did not increase tannase production. Under optimum conditions as standardized here, the enzyme production was 69 U/g dry substrate. This is the first report on production of tannase by A. ruber, giving higher yield under SSF with agro-waste as the substrate.     

Fungal cultures of tar bush and creosote bush for production of two phenolic antioxidants (Pyrocatechol and Gallic acid)

‘Tar bush’ and ‘creosote bush’ were substrates of fungal cultivation for tannase production and gallic acid and pyrocatechol accumulation. Aspergillus niger GH1 grew similarly on both plant materials under solid state culture conditions, reaching maximal levels after 4 d. Fungal strain degraded all tannin content of creosote bush after 4 d of fermentation and >75 % of tar bush after 5 d. Higher level of tannase activity was detected in tar bush fermentation. Biotransformation of tannins to gallic acid was high (93 % in creosote bush and 89 % in tar bush). Pyrocatechol was released poorly. Kinetic parameters of tannin conversion were calculated.     

Alternaria alternata as a new fungal enzyme system for the release of phenolic acids from wheat and triticale brans

This study describes the release of antioxidant ferulic acid from wheat and triticale brans by mixtures of extracellular enzymes produced in culture by a strain FC007 of Alternaria alternata, a dark mold originally isolated from Canadian wood log. The genus of the mold was confirmed as Alternaria by 18S ribosomal DNA characterization. Enzyme activities for feruloyl esterase (FAE) and polysaccharide hydrolyzing enzymes were measured, and conditions for release of ferulic acid and reducing sugars from the mentioned brans were evaluated. The highest level of FAE activity (89 ± 7 mU ml⁻¹ fermentation culture) was obtained on the fifth day of fermentation on wheat bran as growth substrate. Depending on biomass and processing condition, up to 91.2 or 72.3% of the ferulic acid was released from wheat bran and triticale bran, respectively, indicating the proficiency of A. alternata extracellular enzymes in plant cell wall deconstruction. The apparent high extraction of ferulic acid from wheat and triticale brans represents a potential advantage of using a whole fungal cell enzyme complement over yields reported previously through an artificial assembly of cloned FAE with a particular xylanase in a cocktail format.     

Production and Partial Purification of Tannase from Aspergillus ficuum Gim 3.6

A novel fungal strain, Aspergillus ficuum Gim 3.6, was evaluated for its tannase-producing capability in a wheat bran-based solid-state fermentation. Thin-layer chromatography (TLC) analysis revealed that the strain was able to degrade tannic acid to gallic acid and pyrogallol during the fermentation process. Quantitation of enzyme activity demonstrated that this strain was capable of producing a relatively high yield of extracellular tannase. Single-factor optimization of process parameters resulted in high yield of tannase after 60 hr of incubation at a pH of 5.0 at 30°C, 1 mL of inoculum size, and 1:1 solid–liquid ratio in the presence of 2.0% (w/v) tannic acid as inducer. The potential of aqueous two-phase extraction (ATPE) for the purification of tannase was investigated. Influence of various parameters such as phase-forming salt, molecular weight of polyethylene glycol (PEG), pH, and stability ratio on tannase partition and purification was studied. In all the systems, the target enzyme was observed to preferentially partition to the PEG-rich top phase, and the best result of purification (2.74-fold) with an enzyme activity recovery of 77.17% was obtained in the system containing 17% (w/w) sodium citrate and 18.18% (w/w) PEG1000, at pH 7.0.     

Isolation of tannase‐producing microbiota from the gastrointestinal tracts of some freshwater fish

Tannins are the most abundant among the plant‐derived antinutrients that bind readily with protein and other macromolecules to form indigestible complexes, thereby reducing the nutritional value of the plant feedstuffs. Presence of tannase‐producing gut microbiota in herbivorous animals has been suggested to overcome the antinutritional effects of tannins. However, this topic has been less investigated in herbivorous/omnivorous fish species. The present study was undertaken to evaluate the presence of tannase‐producing autochthonous microbiota in the gastrointestinal (GI) tracts of some culturable freshwater teleosts and to identify most promising tannase‐producing strains by molecular methods. Isolation and enumeration of tannase‐producing autochthonous microbiota have been carried out in the gut of ten culturable freshwater teleosts, namely catla (Catla catla), silver carp (Hypophthalmichthys molitrix), rohu (Labeo rohita), grass carp (Ctenopharyngodon idella), mrigal (Cirrhinus mrigala), common carp (Cyprinus carpio), bata (Labeo bata), kalbasu (Labeo calbasu), tilapia (Oreochromis mossambicus), and Nile tilapia (Oreochromis niloticus). Culturable heterotrophic and tannase‐producing microbial populations evaluated on tryptone soya agar and selective tannic acid agar media, respectively, revealed the maximum in the hindguts of all fish species studied. Out of 72 tannase‐producing colonies, 18 randomly selected isolates were maintained as pure cultures and evaluated quantitatively for tannase production. Among these, four most promising tannase producers were identified by 16S/26S rDNA sequencing following nucleotide blast and deposited in the National Centre for Biotechnology Information (NCBI) GenBank. The strain LR01 isolated from rohu was a bacterium, Enterobacter asburae (GenBank Accession No. GU939631 ). However, the strains CM02, OM01 and LR03 isolated from mrigal, tilapia and rohu were yeasts and identified as Pichia kudriavzevii (GenBank Accession No. GU939629 ), Candida tropicalis (GenBank Accession No. GU911469 ) and Candida parapsilosis (GenBank Accession No. GU939630 ), respectively. To the authors' knowledge, the present study is the first to report tannase‐producing autochthonous microbiota in the gut of freshwater teleosts. Tannin‐degrading microbiota detected in the present study may endow the fish with some ecological advantages by enabling them to overcome the anti‐nutritional effects of plant tannins.     

一株产虫草素的冬虫夏草内生真菌 Bionectria ochroleuca OS17

虫草素是一种核苷类似物,具有多种药理作用。利用虫草素产生菌发酵的方式获得虫草素,可能是产生虫草素的一种新方法。为筛选能产虫草素的内生真菌,从中国传统的中药冬虫夏草子实体中共分离得到42株真菌,经PDB液体培养后,采用高效液相色谱（HPLC）鉴定其代谢产物。结果表明：菌株OS17的代谢产物中含有虫草素,且虫草素产量为40.16 mg/L。基于形态学特征和ITS序列分析,菌株OS17被鉴定为淡色生赤壳菌(Bionectria ochroleuca)。这是首次从冬虫夏草中分离得到能产虫草素的生赤壳属,表明了内生真菌具有产生多种生物活性物质的潜力。     

Large-scale production of tannase using the yeast <Emphasis Type="Italic">Arxula adeninivorans</Emphasis>

Tannase (tannin acyl hydrolase, EC 3.1.1.20) hydrolyses the ester and depside bonds of gallotannins and gallic acid esters and is an important industrial enzyme. In the present study, transgenic Arxula adeninivorans strains were optimised for tannase production. Various plasmids carrying one or two expression modules for constitutive expression of tannase were constructed. Transformant strains that overexpress the ATAN1 gene from the strong A. adeninivorans TEF1 promoter produce levels of up to 1,642 U L⁻¹ when grown in glucose medium in shake flasks. The effect of fed-batch fermentation on tannase productivity was then investigated in detail. Under these conditions, a transgenic strain containing one ATAN1 expression module produced 51,900 U of tannase activity per litre after 142 h of fermentation at a dry cell weight of 162 g L⁻¹. The highest yield obtained from a transgenic strain with two ATAN1 expression modules was 31,300 U after 232 h at a dry cell weight of 104 g L⁻¹. Interestingly, the maximum achieved yield coefficients [Y(P/X)] for the two strains were essentially identical.     

Endocellulase Production by <Emphasis Type="Italic">Cotylidia pannosa</Emphasis> and its Application in Saccharification of Wheat Bran to Bioethanol

For efficient bioconversion of lignocellulosic materials to bioethanol, the study screened 19 white-rot fungal strains for their endocellulolytic activity and saccharification potential. Preliminary qualitative and quantitative screening revealed Cotylidia pannosa to be the most efficient endocellulase producing fungal strain when compared to the standard strain of Trichoderma reesei MTCC 164. Ensuing initial screening, the production of endocellulase was further optimized using submerged fermentation to recognize process parameters such as temperature, time, agitation pH, and supplementation of salts in media required for achieving maximum production of endocellulase. The strain C. pannosa produced the maximum amount of endocellulase (8.48 U/mL) under submerged fermentation with wheat bran (2%) supplemented yeast extract peptone dextrose (YEPD) medium after an incubation time of 56 h at 30 °C and pH 5.0 at an agitation rate of 120 rpm with a saccharification value of 50.5%. The fermentation of wheat bran hydrolysate with Saccharomyces cerevisiae MTCC 174 produced 4.12 g/L of bioethanol after 56 h of incubation at 30 °C. The results obtained from the present investigation establish the potential of white-rot fungus C. pannosa for hydrolysis and saccharification of wheat bran to yield fermentable sugars for their subsequent conversion to bioethanol, suggesting its application in efficient bioprocessing of lignocellulosic wastes.