异养硝化-好氧反硝化菌Acinetobacter johnsonii sp. N26的脱氮性能及代谢途径

【背景】水体中含氮物质的大量累积会造成水体富营养化、水生生物死亡等问题,严重威胁水生态环境,制约我国环境保护的持续发展。【目的】为去除生活污水中的含氮污染物,从羊粪堆肥中筛选出了一株具有异养硝化-好氧反硝化功能的细菌——约氏不动杆菌Acinetobacter johnsonii sp.N26,研究其脱氮性能和代谢途径。【方法】测定菌株N26在氨氮和硝态氮中的生长和脱氮曲线,通过单因素试验对其脱氮性能进行优化,通过氮平衡分析和功能基因鉴定研究其脱氮代谢途径。【结果】生长和脱氮曲线表明,菌株N26对初始浓度均为50 mg/L的氨氮和硝态氮的去除速度快、效率高,其中9 h内对氨氮的去除效率为95.5%,最大去除速率为5.330 mg/(L·h);15 h内对硝态氮的去除效率为93.6%,最大去除速率为3.147 mg/(L·h),且最终仅有少量硝酸盐、亚硝酸盐积累。脱氮性能优化结果表明,该菌株的最适氮源为氯化铵,最适碳源为丁二酸钠,最适温度为30℃,最适接种量为15%,最适p H值为8.0-9.0,最适碳氮比为15,最适转速为120 r/min,最适氮负荷≤300 mg/L (氨氮)。氮平衡...     

好氧反硝化菌代谢机制及其与重金属相互作用的代谢特征

好氧反硝化是在好氧条件下将NO3--N最终转化为N2的过程.好氧反硝化菌不仅表现出优秀的脱氮性能,可在许多极端条件下生存,还拥有多种重金属耐受性.本文总结了不同重金属Cr(Ⅵ)、Cu(Ⅱ)和Cd(Ⅱ)对好氧反硝化菌脱氮效率的影响,同时整理了好氧反硝化菌对不同重金属的耐受或去除机制.分析了好氧反硝化菌在工业废水处理中的应...     

海洋环境异养硝化-好氧反硝化菌的研究进展

异养硝化-好氧反硝化（heterotrophic nitrifying-aerobic denitrification,HN-AD）菌的发现打破了传统的脱氮理论,可以在有氧条件下同时进行硝化和反硝化,成为近年来的研究热点。HN-AD细菌在海洋氮循环中发挥着重要作用。本文对海洋环境中HN-AD菌的多样性和部分已知氮代谢途径及相关酶系进行了介绍,分析了盐度、碳氮比、溶解氧、pH等环境因素对HN-AD菌脱氮效果的影响,对其工艺和技术应用、前景和发展方向进行了综述和展望。     

耐低温好氧反硝化菌Aeromonas sp.的分离鉴定及脱氮条件优化

【目的】从冬季活性污泥和河水底泥中分离筛选得到耐低温好氧反硝化菌，并对影响脱氮的关键因子进行优化，以提高低温条件下的脱氮效果。【方法】采用富集纯化法分离筛选耐低温好氧反硝化菌株。通过形态观察和16S rRNA基因系统发育分析等方法对筛选菌株进行菌种鉴定。以NO3–-N去除率为响应目标，采用Box-Behnken试验设计及响应面回归分析法优化影响脱氮效果的关键因子（C/N、温度、pH和摇床转速），确定最佳培养条件。【结果】从东北寒冷地区冬季河水底泥样品中分离得到的一株耐低温好氧反硝化菌Z6，菌落呈白色半透明圆形，菌体细胞为短杆状，大小为（0.8–1.6）μm×（0.6–0.8）μm，革兰氏染色阴性。与气单胞菌属（Aeromonas）的16S rRNA基因序列高度同源，鉴定该菌为气单胞菌。采用响应面分析方法得到菌株Aeromonas sp. Z6的最佳脱氮条件为：C/N 5.9，温度12°C,pH 6.8，摇床转速155 r/min，在此条件下对NO₃^–-N的去除率为89.72%，与预测值（90.34%）无显著差别。【结论】首次报道气单胞菌（Ae...     

极端条件下异养硝化-好氧反硝化菌脱氮的研究进展

异养硝化-好氧反硝化(HN-AD)是对传统自养硝化异养反硝化理论的丰富与突破。HN-AD菌在好氧条件下可快速实现氨氮、硝态氮(NO_3~–-N)、亚硝态氮(NO_2~–-N)三氮同步脱除。它们不仅具有分布范围广、适应能力强、代谢通路特殊等特点,而且还具有世代时间短、脱氮速率快、高活性持久等独特优势,在高盐、低温、高氨氮等极端条件表现出了巨大的脱氮潜力,因此在废水生物脱氮领域受到广泛关注。文中在介绍HN-AD菌属类别及代谢机理的基础上,重点总结了在高盐、低温、高氨氮等极端条件下进行氨氮脱除的HN-AD种属,系统分析了它们在极端条件下的脱氮特性及潜力,并简述了HN-AD菌在极端条件下的工艺应用研究进展,最后展望了HN-AD脱氮技术的应用前景和研究方向。     

好氧反硝化菌的选育及其初步应用

采用间歇曝气、极限稀释和酸碱指示剂培养基相结合的办法,从池塘底泥中成功分离到好氧反硝化菌株H2,经生理生化和16S rDNA序列分析,初步判断为芽孢杆菌属(Bacillus sp.).在室内模拟养殖水体中,菌株H2在15 d中对亚硝酸盐和硝酸盐的最高降解速率分别达到0.885 mg/L·d和0.46 mg/L·d,试验结束时,总氮去除率达到45.2%.结果表明,菌株H2具有应用于养殖水体生物脱氮领域的巨大潜力.     

异养硝化-好氧反硝化细菌的研究进展

异养硝化-好氧反硝化菌株的发现是对传统硝化反硝化的突破和发展。近年来由于其独特的生物学特性及其在污水处理中的巨大优势,受到众多学者的青睐。文章介绍了异养硝化-好氧反硝化菌的筛选,异养硝化-好氧反硝化代谢途径和异养硝化-好氧反硝化菌的影响因素,并总结了异养硝化-好氧反硝化菌在废水处理中的研究进展,最后展望未来研究的方向。     

一株好氧反硝化细菌的分离鉴定及反硝化特性研究

通过对采集水样进行富集培养,利用溴百里酚蓝( BTB)选择性培养基初筛和活性测定复筛得到一株好氧反硝化细菌N22’,发现该菌在好氧条件下能有效去除培养液中的NO3--N.硝酸盐氮初始浓度为125 mg/L,培养40h后硝酸盐氮去除率达86.39％;扫描电镜照片显示,菌株N22’为短杆菌,无鞭毛,大小约为(0.75-1.25)μm×(0.5-0.75) μm范围内,菌落表面呈乳白色.通过形态、生理生化特征及16S rRNA基因序列分析,初步判断菌株N22’为不动杆菌属Acinetobacter sp..反硝化性能测试结果表明,该菌反硝化作用的最适温度为25-30℃,pH值7.0.     

异养硝化-好氧反硝化的研究进展

近年来,异养硝化-好氧反硝化菌的发现打破了传统硝化反硝化理论,其在去除氮素和有机污染物的同时,能够实现同时硝化反硝化(SND),因此受到广泛关注。文章介绍了异养硝化-好氧反硝化菌的影响因素和一些已筛选菌的最佳脱氮效果,及其与传统硝化反硝化菌作用酶系的不同,列出了一些已筛选菌的氮代谢途径,并对中间产物NO2--N积累和复合菌方面的研究进展进行了综述,最后提出了异养硝化-好氧反硝化在生物强化应用中的研究现状和面临的挑战。     

一株异养硝化-反硝化不动杆菌的分离鉴定及脱氮活性

[目的]分离筛选并鉴定一株异养硝化-反硝化细菌,并探讨其在脱氮中的作用.[方法]富集培养分离筛选微生物,通过形态观察和生理生化特征及16S rDNA鉴定细菌,定时测定其OD600研究生长曲线,正交试验研究其脱氮影响因素和最佳条件,与污水处理厂活性污泥共同作用检验其脱氮活性.[结果]分离到一株异养硝化-反硝化细菌,鉴定结果表明是一株不动杆菌,命名为Acinetobacter sp.YF14,这是已知报道的第一株进行异养硝化和好氧反硝化的不动杆菌.该菌在12 h时进入对数期,22 h时进入稳定期,45 h以后进入衰亡期.该菌能进行异养硝化,3d后氨氮和总氮的去除率可以达到92％和91％,且无硝酸盐氮和亚硝酸盐氮积累.好氧条件下该菌能进行反硝化,在硝酸盐和亚硝盐培养基中均能将氮几乎完全去除.对该菌脱氮的影响程度大小依次为转速＞接种量＞碳源＞碳氮比＞ pH.当转速为160 r/min,碳源取葡萄糖,接种量1％,碳氮比为8∶1,pH为6.5时,脱氮效果最好.该菌株可以提高活性污泥对于生活污水总氮脱除率约30％.[结论]菌YF14可以明显加强活性污泥脱氮效果,显示了良好的应用前景.     

不动杆菌Acinetobacter sp. TAC-1利用聚(3-羟基丁酸酯-co-3-羟基戊酸酯)的碳代谢机理

为阐明异养硝化-好氧反硝化(heterotrophic nitrification-aerobic denitrification, HN-AD)菌株不动杆菌(Acinetobactersp.)TAC-1利用聚(3-羟基丁酸酯-co-3-羟基戊酸酯)[poly(3-hydroxybutyrate-co-3-hydroxyvalerate), PHBV]的碳代谢途径,以乙酸钠(sodium acetate, SOA)为对照,考察TAC-1菌株基因水平上存在的碳水化合物代谢通路。全基因组测序结果表明,TAC-1菌株中存在gltA、icd、sucAB、acs和pckA等碳水化合物代谢酶编码基因;KEGG通路数据库注释进一步证实TAC-1菌株存在糖酵解途径(glycolyticpathway,EMP)、磷酸戊糖途径(pentosephosphate pathway, PPP)、乙醛酸循环(glyoxylate cycle, GAC)和三羧酸循环(tricarboxylic acid cycle, TCA cycle)等碳水化合物代谢通路;不同碳源的代谢物差异表达,进一步证实TAC-1菌利用PH...     

Evaluation of the strains of Acinetobacter and Enterobacter as potential biocontrol agents against Ralstonia wilt of tomato

Bacterial wilt (Ralstonia solanacearum) of tomato, Lycopersicon esculentum, causes a considerable amount of damage to tomato in Southern China. Biological control is one of the more promising approaches to reduce the disease incidence and yield losses caused by this disease. Based on antagonistic activity against R. solanacearum and three soil-borne fungal pathogens as well as biocontrol efficacy in the greenhouse, two bacterial strains Xa6 (Acinetobacter sp.) and Xy3 (Enterobacter sp.) were selected out of fourteen candidates as potential biocontrol agents. In order to find a suitable antagonist inoculation method, we compared the methods of root-dipping with soil-drenching in the aspects including rhizocompetence, biocontrol efficacy, and effect of promoting plant growth under greenhouse conditions. The drenching treatment resulted in a higher biocontrol efficacy and plant-yield increase, and this method was also easier to operate in the field on a large scale. Field trials were conducted for further evaluation of these two antagonistic strains. In both greenhouse and field experiments, the strain Xy3 had a better control effect against bacterial wilt than Xa6 did, while Xa6 caused higher biomass or yield increases. As recorded on the 75th day after treatment in two field experiments, biocontrol efficacy of Xy3 was about 65% in both field trials, and the yield increases caused by Xa6 were 32.4 and 40.7%, respectively, in the two trials. This is the first report of an Acinetobacter sp. strain used as a BCA against Ralstonia wilt of tomato.     

微生物驱动硝酸盐还原耦合亚铁氧化成矿过程的锌胁迫

【目的】探究中性厌氧条件下,金属锌影响下硝酸盐依赖型铁氧化菌Pseudomonas stutzeri LS-2驱动的硝酸盐还原耦合亚铁氧化成矿过程机制,对深入理解中性厌氧环境中微生物亚铁氧化驱动的反硝化作用及重金属固定机制具有重要意义。【方法】以不同Zn(Ⅱ)浓度构建LS-2驱动的亚铁氧化成矿体系,分析不同体系中亚铁氧化速率、硝酸盐还原速率以及形成矿物的结构变化规律。【结果】LS-2驱动的硝酸盐还原耦合亚铁氧化成矿过程中,共存Zn(Ⅱ)降低该过程中硝酸盐的还原速率和亚铁氧化速率。同时,随着Zn(Ⅱ)浓度提高,抑制作用增强。微生物亚铁氧化形成的矿物通过吸附、共沉淀和离子置换等过程固定Zn(Ⅱ),降低Zn(Ⅱ)活性。Zn(Ⅱ)浓度对形成的矿物结构有较大的影响:低浓度Zn(Ⅱ)体系中,形成的矿物为纤铁矿;随着Zn(Ⅱ)浓度的提高,矿物结构与结晶度都有一定程度的变化,当Zn(Ⅱ)达到4 mmol/L时,形成的矿物主要为铁锌尖晶石。【结论】明确了重金属锌对LS-2菌株反硝化及亚铁氧化过程的抑制规律,同时阐明了Zn(Ⅱ)浓度对形成矿物结构的影响。研究结果有助于深入认识中性厌氧环境中重金属与微生物驱动的铁循环和反硝化过程的耦合作用,为土壤重金属污染防治提供理论支撑。     

禾谷镰刀菌拮抗菌21-6的鉴定及其抑菌活性测定

【背景】禾谷镰刀菌（Fusarium graminearum）是一种危害小麦生产的重要病原真菌。【目的】筛选对禾谷镰刀菌具有拮抗活性的链霉菌菌株,为该病原的生物防治提供理论基础。【方法】采用稀释涂布法分离链霉菌,利用平板对峙法筛选高活性拮抗菌株;通过形态学、生理生化特征和16S rRNA基因序列分析确定其分类地位;采用生长速率法分析其发酵条件及无菌发酵液的稳定性;并测定该菌株的防病效果和抑菌谱。【结果】筛选到一株对禾谷镰刀菌具有较强抑制作用的链霉菌菌株21-6,抑菌率为75.2%±2.1%。根据形态学、生理生化特征及16S rRNA基因序列分析,将其鉴定为Streptomyces stelliscabiei。菌株21-6在pH为中性条件下的PDB培养基中培养5 d能够产生更好的抑菌效果。无菌发酵液能够抑制禾谷镰刀菌的菌丝生长和孢子萌发过程。无菌发酵液不受高温、胃蛋白酶、胰蛋白酶及蛋白酶K的影响,耐酸但对碱性条件敏感。发酵液对禾谷镰刀菌侵染小麦胚芽鞘具有抑制效果。菌株21-6具有聚酮合酶pks-Ⅰ和pks-Ⅱ基因。此外,该菌株对5种植物病原真菌均具有抑制效果。【结论】链霉菌菌株21-6对禾谷镰刀菌具有较好的生防潜力。     

Reduction of Cr(VI) by a Bacillus sp.

A Bacillus sp. RE was resistant to chromium and reduced Cr(VI) without accumulating chromium inside the cell. When Cr(VI) was 10 and 40 μg ml⁻¹, >95% of the total Cr(VI) was reduced in 24 and 72 h of growth, respectively, whereas at 80 μg Cr(VI) ml⁻¹ only 50% of Cr(VI) was reduced. However growth was not affected; the cell mass was 0.7–0.8 mg ml⁻¹ in all cases. The cell-free extract showed Cr(VI) reducing enzyme activity which was enhanced (>5 fold) by NADH and NADPH. Like whole cells the enzyme also reduced Cr(VI) with decreasing efficiency on increasing Cr(VI) concentration. The enzyme activity was optimal at pH 6.0 and 30 °C. The enzyme was stable up to 30 °C and from pH 5.5 to 8, but from pH 4 to 5 the enzyme was severely destabilized. Its K_m and V_max were 14 μm and 3.8 nmol min⁻¹ mg⁻¹ respectively. The enzyme activity was enhanced by Cu²⁺ and Ni²⁺ and inhibited by Hg²⁺. Received 21 September 2005; Revisions requested 5 October 2005; Revisions received 16 November 2005; Accepted 16 November 2005     

颈盲蝽取食对薇甘菊叶片营养物质和防御酶的影响

【目的】薇甘菊是世界最具危害性的入侵杂草之一,对我国生态环境和农业、林业生产造成了严重的危害。颈盲蝽是控制薇甘菊的一种潜在的重要天敌昆虫。本研究旨在探讨薇甘菊被颈盲蝽取食后,叶片防御相关酶系活性、营养物质和叶绿素含量的变化,阐明颈盲蝽取食对薇甘菊生理功能的影响,为利用颈盲蝽防控薇甘菊提供依据。【方法】从云南瑞丽野外采集薇甘菊的本地天敌昆虫颈盲蝽,测定了颈盲蝽取食前及取食12、24、48、96 h后,薇甘菊叶片中过氧化物酶(POD)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)活性,以及可溶性糖、可溶性蛋白及叶绿素含量,以取食前的植株作为对照。【结果】与对照相比,颈盲蝽取食12 h时,薇甘菊叶片中的POD、CAT活性升高,SOD活性降低;之后POD、SOD活性上升,CAT活性降低,取食48 h时,POD和SOD活性达到最高值,CAT活性达到最低值;取食96 h时,POD与SOD活性降低,但仍高于对照,CAT活性与取食48 h时相近。颈盲蝽取食后,薇甘菊叶片中的可溶性糖含量明显上升,取食96 h达到最高值;可溶性蛋白和叶绿素含量显著降低,在96 h达到最低值,分别低于对照39.30%和69.94%。【结论】颈盲蝽取食严重破坏了薇甘菊叶片的正常生理功能,并最终导致其叶片萎蔫和坏疽。     

Bullera begoniae sp. nov. and Bullera setariae sp. nov., two new species of ballistoconidium-forming yeasts in the Bullera variabilis (Bulleribasidium) cluster isolated from plants in Taiwan

Two strains of xylose-containing and Q-10-having ballistoconidiogenous yeasts isolated from plant leaves collected in Taiwan were found to represent two new species of the genus Bullera. In the phylogenetic trees based on the sequence analysis of 18S rDNA and D1/D2 domain of 26S rDNA, these species are located in the Bullera variabilis (Bulleribasidum) cluster in Hymenomycetes. They are described as Bullera begoniae sp. nov. and Bullera setariae sp. nov., respectively.     

Transition metal-saccharide chemistry: d-glucose complexes of Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)

Metal complexes of d-glucose (d-Glc) from large cation containing dibromo-dichloro salts of dipositive metals [NEt₄]₂[MBr₂Cl₂] (M = Mn, Co, Ni, Cu and Zn) and the disodium salt of glucose were synthesized from a MeOH:MeCN mixture. The complexes were characterized by UV-vis absorption, circular dichroism, IR and proton magnetic resonance spectroscopies, and by elemental analysis, and were found to be Na[M(d-Glc)(OMe)Cl]. Cyclic voltammetric studies of these complexes, in the acidic to neutral pH range, indicated no dissociation, even in highly acidic conditions.This paper is dedicated to Professor Richard H. Holm (Harvard University) on the occasion of his 60th birthday.     

Combination of ARDRA and RAPD genotyping techniques in identification of Acinetobacter spp. genomic species

A total of 10 non-repetitive multi-drug-resistant Acinetobacter strains were collected. With reference to A. calcoaceticus (ATCC23055), A. baumannii (ATCC19606), A. lwoffii (ATCC17986), and A. junii (NCTC5866),DNA fingerprint technique, amplified ribosomal DNA restriction analysis (ARDRA), and random amplified polymorphism DNA (RAPD) were carried out to identify the genomic species of Acinetobacter spp. The distances between them were calculated by the unweighted pair group method with arithmetic (UPGMA). Genotypes of Acinetobacter spp. were effectively classified and an A. junii together with nine A. baumannii isolates was genomically identified. The combination of ARDRA and RAPD DNA-fingerprint technique shows high complementarity, and could be a useful tool in Acinetobacter genomic species identification. __________ Translated from Microbiology, 2007, 34(2): 303–306 [译自:微生物学通报]