好氧反硝化菌的筛选及其脱氮除磷性质的研究

利用富集培养基, 从用生活污水驯化后的活性污泥中筛选得到一株具有好氧反硝化兼具除磷功能的细菌。通过形态学及生理生化指标鉴定其为假单胞菌属。利用此好氧反硝化菌处理模拟废水及生活废水, 通过监测总氮、无机磷及CODcr变化确定在C/N摩尔比为3:1、接种量为10%、pH 6.8、30°C条件下处理2 d, 该菌株脱氮、除磷及去除有机物的效果最佳, 活性污泥经此好氧反硝化菌强化后, 对生活废水的处理能力得到明显提升。     

一株耐盐菌Halomonas sp. A20的分离及降解糖精钠废水的特性

【背景】糖精钠废水是一种难处理的高盐有机工业废水。【目的】为了提高糖精钠废水的生物降解效果,需要研究糖精钠废水降解菌的特性。【方法】采用纯培养技术从处理糖精钠废水的多级生物接触氧化系统内的活性污泥中分离筛选糖精钠废水降解菌,对分离菌株的形态特征、生理生化特性和16S rRNA基因序列进行分析,利用单因素实验和响应面法考察分离菌株降解糖精钠废水的最佳条件。【结果】筛选获得一株糖精钠废水降解菌A20,归属于盐单胞菌属(Halomonas),当糖精钠废水的盐分为5%,菌接种量为15%,pH值为8.0,温度为30°C时,菌株A20对糖精钠废水中的化学需氧量(chemical oxygen demand,CODcr)去除率在60%以上;通过响应面法优化,菌株A20降解糖精钠废水的最佳条件为：pH 8.0,温度为30.3°C,接种量为14.1%,其CODcr去除率为65.4%。【结论】分离到一株能高效降解糖精钠废水中有机物的耐盐菌Halomonas sp. A20,可为高盐、高浓度糖精钠废水的处理提供优良的微生物菌种资源。     

2株耐低温微生物处理污水模拟试验初报

从下水管道的污泥中分离筛选到耐冷细菌H6和耐冷酵母菌J1,采用此2菌株进行模拟污水低温(8℃)处理试验。H6和J1菌株对模拟污水COD的去除率分别为66.6%和72.2%;H6、J1菌株对有机氮去除率分别为76.9%和64.5%;H6、J1菌株对总磷去除率分别为53.9%和14.0%。说明低温微生物在低温环境的污水处理具有广阔的应用前景。     

阿特拉津降解菌株的分离、鉴定和工业废水生物处理试验

用液体无机盐培养基富集培养法和无机盐平板直接分离法, 从生产阿特拉津的农药厂的废水和污泥混合物中分离到13个能以阿特拉津为唯一氮源生长的细菌菌株。通过16S rRNA基因序列分析, 11个菌株被鉴定为Arthrobacter spp., 2个菌株被鉴定为Pseudomonas spp.。对阿特拉津降解活力最高的Arthrobacter sp. AD30和Pseudomonas sp. AD39的降解基因组成和降解特性进行了详细研究。降解基因的PCR扩增表明, AD30和AD39都含有trzN-atzBC基因, 能将有毒的阿特拉津降解成无毒的氰尿酸。降解实验表明, 向阿特拉津浓度为200 mg/L的无机盐培养基中分别接种等量的AD30、AD39和这两个菌株的混合菌液, 30°C振荡培养48 h以后, 阿特拉津去除率分别为92.5%、97.9%和99.6%, 表明混合菌的降解效果好于单菌。用AD30和AD39的混合菌液接种阿特拉津浓度为176 mg/L的工业废水, 30°C振荡培养72 h以后, 99.1%的阿特拉津被去除, 表明混合菌株在阿特拉津工业废水的生物处理中有很好的应用潜力。     

一株轻度嗜盐反硝化细菌的分离鉴定和反硝化特性初探

从处理高盐度废水的成熟活性污泥中分离筛选得到1株轻度嗜盐反硝化细菌GYL, 通过对该菌株的形态观察、生理生化实验以及16S rDNA序列分析, 确定该菌株为盐单胞菌(Halomonas sp.)。该菌株能在盐度为10%的培养液中生长, 最适盐度为2%~7%, 最适pH为7.5~8.5, 最佳碳源为蔗糖, 在25°C~30°C的温度范围内脱氮效率达到80%以上。对该菌株的异养硝化能力进行了测定, 其对氨氮的去除率可达98.3%, 说明该菌株可实现同步硝化反硝化, 即该菌可以独立完成生物脱氮的全部过程。     

低温污水中耐冷微生物的筛选及多样性分析

采用4种分离培养基对新疆乌鲁木齐市污水处理厂低温污水中的耐冷微生物进行分离筛选, 共获得各种耐冷微生物154株, 其中丝状真菌12株, 酵母46株, 放线菌6株, 细菌90株。并对部分菌株的耐受性和产酶特性进行了研究, 获得了耐4%NaCl的菌株44株, 耐0.2%苯酚的16株, 耐0.5% SDS的33株, 具有淀粉酶活性的菌株40株, 蛋白酶活性的30株, 脂酶活性的27株。对其中60株细菌进行16S rRNA基因测序, 序列比对分析表明, 其分属13个属, 其中菌株39与不动杆菌属中的标准菌株Aci     

光合细菌利用工业有机废水产生5-氨基乙酰丙酸

[目的]利用本实验室筛选的5-氨基乙酰丙酸(5-aminolevulinic acid,ALA)高产紫色非硫红假单胞菌株,以味精、柠檬酸、啤酒和豆制品生产废水作为底物,进行光合细菌利用废水产生ALA并去除化学需氧量(CODcr)的研究.[方法]光合细菌培养温度为30℃,光照强度为3000 Lux,进行乙酰丙酸、甘氨酸、琥珀酸的添加与否和废水灭菌与否的处理,用比色法测定菌液光密度,ALA检测采用Ehrlich'S试剂分光光度检测法.[结果]在不添加乙酰丙酸(levulinic acid,LA)、甘氨酸和琥珀酸的条件下,菌株99-28的菌体生长在72～96 h达到稳定期,ALA产量在96h最高,在4种废水中,味精废水的ALA产量最高,CODcr去除率也最高;添加LA、甘氨酸和琥珀酸显著提高ALA产量,但CODcr去除效果不好.废水不灭菌略微降低99-28菌株的生长和CODcr的去除能力,在添加LA、甘氨酸和琥珀酸的条件下的,ALA产量明显下降.ALA高产突变菌株L-1在有机废水中的生长状况、对有机废水的CODcr去除与菌株99-28表现一致,在不添加和添加LA、甘氨酸和琥珀酸的条件下,突变株L-1的ALA产量明显比菌株99-28高.[结论]本实验室筛选的紫色非硫红假单胞菌株能利用有机废水作为底物产生ALA并降解CODcr.     

生物淋滤法去除污泥中的重金属

本研究从剩余活性污泥中分离得到两株土著硫杆菌。对两株菌进行了分类鉴定。确立二者分别为嗜酸性氧化亚铁硫杆菌(Acidithiobacillus ferrooxidans, A. f)和嗜酸性氧化硫硫杆菌(Acidithiobacillus thiooxidans, A. t)。将二者的单菌和混合菌分别接种于剩余活性污泥中, 进行了为期9 d的生物淋滤, 对淋滤过程中的pH变化、氧化还原电位(ORP)以及重金属含量进行了检测。结果表明, 生物淋滤9 d混合菌对于As、Cr、Cu、Ni和Zn的去除效果最好; 去除率分别达到了96.09%、93.47%、98.32%、97.88%和98.60%。对于Cd和Pb混合菌生物淋滤的去除率在第6天之后迅速下降, 但是A. t单菌淋滤保持较高的去除率。     

嗜盐菌对高盐有机废水处理的强化作用

为解决高盐有机工业废水处理这一难题, 从山东省威海市路道口盐场晒盐池盐水中分离一株嗜盐菌株YS-1, 通过对该菌株进行原子力显微镜观察、生理生化测定、全细胞脂肪酸分析和16S rDNA序列同源性分析发现YS-1菌株16S rDNA序列与Halomonas sp. (AB167061)的亲缘关系最为接近, 结合上述其它各项结果确定该菌株为盐单胞菌属(Halomonas sp.), 属中度嗜盐菌; 在SBR反应器中对该菌株进行强化高盐有机废水处理试验, 结果表明, 含盐12%、CODcr=1494 mg/L的高盐模拟有机废水, 经72 h CODcr去除率为90.0%, 120 h的CODCr去除率为98.1%, 该菌株具有强化高盐有机废水处理的功能, 通过分离筛选嗜盐菌强化高盐有机工业废水处理具有可行性。     

孔雀石绿脱色菌恶臭假单胞菌菌株M6的分离、鉴定及其生长特性研究

从养殖池污泥中分离了6株对孔雀石绿具有脱色能力的菌株, 经过进一步在孔雀石绿营养肉汤中富集培养及其脱色率的比较, 筛选出对孔雀石绿具有较强脱色能力的优良菌株M6。菌株M6在30°C、150 r/min条件下对孔雀石绿的脱色率为97.14％, 通过革兰氏染色、电镜对其形态进行了观察, 用ATB细菌鉴定仪对其进行了生理生化鉴定; 通过对其16S rDNA序列进行PCR扩增和测序, 与NCBI中收录的与其同源性较高的菌株进行了聚类分析并构建了系统发育树。此外, 对其生长特性也进行了研究。实验结果表明, 菌株M6革兰氏染色阴性, 杆形, 端生一根鞭毛, 大小约为0.45 mm×0.84 mm, 在孔雀石绿营养琼脂平板上形成的菌落特征为圆形、浅蓝色、粘稠、不易挑取; 菌株M6的16S rDNA序列与GenBank基因库中假单胞菌属的细菌菌株的16S rDNA序列有98％~99％的高度同源性, 菌株M6与恶臭假单胞菌OW-16(登录号：DQ112328.1)的亲缘关系最近。结合传统的形态与生理生化特性鉴定以及16S rDNA序列分析鉴定的结果, 判定菌株M6为恶臭假单胞菌(Pseudomonas putida)(登录号：EU348741.1)。此外, 菌株M6在30°C、150 r/min条件下摇床振荡培养的生长曲线为：0 h~4 h为生长延迟期, 4 h~64 h为对数生长期, 64 h~80 h为稳定期, 80 h以后为衰亡期; 其最适生长pH值为7, 最适生长温度为30°C, 在转速为50 r/min~250 r/min条件下, 其浓度随转速的增加而增大。     

六种藓类植物茎的比较解剖学研究

通过对6种藓类植物,即褶叶青藓(Brachythecium salebrosum(Web.et Mohr.)B.S.G.)、湿地匐灯藓(Plagiomnium acutum(Lindb.)Kop.)、侧枝匐灯藓(Plagiomnium maximoviczii(Lindb.)Kop.)、大凤尾藓(Fissidensnobilis Griff.)、大羽藓(Thuidium cymbifolium(Doz.et Molk.)B.S.G.)和大灰藓(Hypnum plumaeforme Wils.)嫩茎和老茎的石蜡切片和显微观察发现,同一藓类植株的嫩茎和老茎,茎结构稳定,不同种藓类植物茎横切面具有不同特征.植物体茎横切面形状、表层细胞的层数、细胞大小和细胞壁厚薄、皮层细胞大小和形状、中轴的有无以及比例等特征可以作为藓类植物的分科分类依据之一.     

Cause of Senescence of Nine Sorts of Flowers

The levels of endogenous phytohormones and respiratory rate in nine sorts of flowers such as Cymbidium faberi Rolfe, Nopalxochia ackermannii Kunth and others were investigated both at full bloom and senescence and meanwhile the effect of exogenous phytohormones on prolonging the blossoms and promoting ethylene production were tested. There is a high content of endogenous ethylene in all the long-lived flowere, about 3–16 folds higer than the short-lived ones. There is a high level of ABA at full blooming flowers of short-lived flowers, in which there is no or only some cytokinins in it, but the ratio of CTK (6BA+zeatin)/ABA is smaller(l.7). The endogenous ABA reached a much higher level at senescence in all nine sorts of flowers, so it is reasonable to consider that it is ABA which plays an important role of regulation in controlling flower's senescence. There is a much higher level of GA3 and zeatin in the long-lived flowers which is not demonstrated in the shortlived ones. The respiratory rate is one of the factors controtling the longevity of flowers, but it does not play a decided role. Application of 6BA and zeatin prolongs distinctly orchid’s longevity, however exogenous IAA through the promotive action on ethylene production, evidently extends the longevity of the flowers of the Nopalxochia ackermannii Kunth.     

龙胆科药用植物化学成分的研究现状

龙胆科植物在我国的分布范围很广,且多数为药用植物,其多数种属的药用植物,至今其化学成分尚未被系统研究。综述了目前龙胆科药用植物的化学成分的研究现状及一般提取方法,对近年来发现的环烯醚萜及裂环烯醚萜类化合物进行了总结,为本科药用植物的更深入研究提供了参考。     

The effects of glutamine of the maintenance of embryogenic cultures of Cryptomeria japonica

Summary Embryogenic tissues of sugi (Cryptomeria japonica) were induced on a modified Campbell and Durzan (CD) medium containing 1 μM 2,4-dichlorophenoxyacetic acid (2,4-D) and 600 mg l⁻¹ glutamine, and subcultured in the medium of the same composition for over 1 yr. This resulted in a mixed culture of embryogenic and non-embryogenic cells. When embryogenic cells were isolated and cultured independently, their capacity to form embryogenic aggregates was lost. Thus, the non-embryogenic cells present within a mixed culture system were essential to the formation of embryogenic aggregates. When embryogenic tissues were isolated and cultured independently on a high glutamine-containing (2400 mg l⁻¹) medium, dry weights and endogenous levels of glutamine increased, and the tissue could generate a large number of embryogenic aggregates. Amino acid analysis of embryogenic and non-embryogenic cells from the maintenance culture indicated a higher level of glutamine was present in the latter. The high endogenous level of glutamine in the non-embryogenic portion of mixed cell masses may be the supplier of glutamine for maintaining the embryogenic property of the tissues.     

Specificity of action of piperidylcholine derivatives as substrates of cholinesterases of various origin

The review deals with study of enzymologic properties of a novel highly specific acetylcholinesterase substrate, N-(β-acetoxyethyl) piperidinium iodomethylate (“piperidylcholine”), and its 30 derivatives that were tested as effectors of cholinesterases of mammals and various species of Pacific squids. It was proven for the first time that responsible for specificity of action was structure of cyclic ammonium grouping of the alcohol part of molecule of the ester substrate. Analysis of specificity is performed based on enzymatic hydrolysis parameters—activity of catalytic center of cholinesterases and bimolecular constant of the reaction rate that are determined at optimal and low substrate concentrations. Among the specially synthesized group of thioester compounds there is revealed one more highly specific acetylcholinesterase substrate—N-(β-acetoxyethyl) piperidinium.     

真菌类遗传学分析的知识结构教学

本文以认知结构理论为指导,讨论了真菌类遗传分析与高等动植物遗传分析的内在联系,认为利用这种内在联系进行教学可收到好的效果并说明了作者的具体教学过程。 Abstract:In the paper, the relationship between genetic analysis of Fungi and genetic analysis of high animal and plant was discussed.A good results were obtained when we adopted this method in the teaching.     

Photoregulation of seed germination of wild-type and of an aurea-mutant of tomato

Seed germination of an aurea mutant of tomato ( Lycopersicon esculentum Mill.) is promoted by continuous irradiation with red, far-red or long-wavelength far-red (758 nm) light as well as by cyclic irradiations (5 min red or 5 min far-red/25 min darkness). Far-red light applied immediately after each red does not change the germination behaviour. Seed germination of the isogenic wild-type, cv. UC-105, is promoted by continuous and cyclic red light while it is inhibited by continuous and cyclic far-red light and by continious 758 nm irradiation. Far-red irradiation reverses almost completely the promoting effect of red light. The promoting effect (in the aurea mutant) and the inhibitory effect (in the wild-type) of continuous far-red light do not show photon fluence rate dependency above 20 nmol m⁻² s⁻¹. It is concluded that phytochrome controls tomato seed germination throgh low energy responses in both the wild type and the au mutant. The promoting effect of continuous and cyclic far-red light in the au mutant can be attributed to a greater sensitivity to P_fr.     

The mechanism of hatching of eggs of Haemonchus contortus

Fluid collected from hatching eggs of Haemonchus contortus contained a lipase which hydrolysed 2-naphthyl laurate (about 0·7 μmol naphthol freed /h/10⁶ eggs). The fluid also hydrolysed l-leucinamide (about 2·3 μmol leucine freed/h/10⁶ eggs). The fluid when added to normal or heated eggs caused ‘hatching’. ‘Hatching’ also occurred in exsheathing fluid from infective juveniles and in a preparation of pancreatic lipase containing leucine aminopeptidase. A purified mammalian leucine aminopeptidase in combination with several different lipases did not attack egg shells.The ‘spontaneous’ hatching of eggs of H. contortus was strongly inhibited by 1,10-phenanthroline, 10^?3M, and this inhibition was reversed by Zn²⁺. However, the inhibition of ‘hatching’ of eggs in externally applied hatching fluid, or the hydrolysis of leucinamide in hatching fluid was generally less marked.