微生物絮凝剂产生菌的筛选及其培养条件优化

从广西大学食用菌废弃料中分离出7株絮凝剂产生菌,以发酵液对高岭土悬浮液絮凝效果为指标衡量其絮凝活性及产絮凝剂能力,经过初筛与复筛,筛选到一株絮凝剂高产菌F00,初步确定属曲霉属(Aspergillus),并对其产生絮凝剂的条件进行优化.     

高效微生物絮凝剂产生菌TJ-3的絮凝特性分析

从活性污泥中分离筛选出一株高效絮凝剂产生菌TJ-3, 经生理生化试验检测其属于革兰氏阴性菌, 短杆状, 16S rDNA测序鉴定为铜绿假单胞菌。生长曲线表明, TJ-3的生长稳定期较长, 所产微生物絮凝剂(MBF)的稳定性良好。TJ-3产MBF对高岭土悬液具有良好的絮凝效果, 最佳条件下的絮凝率为98.2%。絮凝活性分布实验结果表明, TJ-3所产MBF的活性物质大部分存在于离心后的沉淀物中。处理100 mL高岭土悬液, pH值8.5、1%(质量分数)CaCl2溶液投加量3.5 mL、菌液投加量1.5 mL时, 絮凝效果最佳。     

微生物絮凝剂产生菌的筛选及培养条件的优化

目的:从好氧活性污泥、土壤和河泥中分离筛选具有较高活性的絮凝剂产生菌,并优化其培养条件;方法:通过常规分离获得目的菌株,运用单因素法考察培养时间、培养温度、发酵液初始pH值及摇床转速对菌株絮凝活性的影响;结果:得到了絮凝活性较高的菌株,经过优化得出,其最佳培养时间和温度分别为48h和30℃,发酵液最佳初始pH值为7.0,最佳摇床转速为120r/min,在最佳培养条件下,RF-32对高岭土悬浊液絮凝率为84.32%。结论:从活性污泥中可筛选出较高活性的絮凝剂产生菌,研究发现,菌株的絮凝活性与其生长量呈同步增长趋势,并在一段时间后达到一稳定值。培养时间、培养温度、发酵液初始pH值及摇床转速均能通过一定的作用因素对菌株生长情况产生影响,进而影响其絮凝活性。     

高效微生物絮凝剂D6对屠宰废水的应用研究

筛选出一株针对屠宰废水有高效絮凝活性的微生物絮凝剂产生菌,并对其所产微生物絮凝剂D6进行单因子絮凝条件优化和正交试验优化得到最佳絮凝条件。絮凝条件包括:微生物絮凝剂D6投加量、pH、金属离子种类、1%CaCl₂投加量。试验中发现碱性环境是微生物絮凝剂D6发挥絮凝活性的前提,表明微生物絮凝剂D6分子链的充分伸展对絮凝作用起决定因素,因此微生物絮凝剂D6的絮凝机理为吸附架桥作用。其最佳絮凝条件为微生物絮凝剂D6的投加量为25mL·L^-1,1%CaCl₂投加量55mL·L^-1,pH为8。在最佳絮凝条件下,絮凝率为96.6%,浊度去除率为97.8%,SS去除率为92.6%。     

一株絮凝剂产生菌的筛选鉴定及培养条件

从淤泥中筛选到1株高效微生物絮凝剂产生菌JX18,经过对其形态特征、生理生化特性、以及16SrRNA序列分析初步鉴定为荧光假单胞菌。该菌培养40h进入稳定期,48h时絮凝活性达到最大。进一步研究表明:菌株JX18最适培养基初始pH值7.0,培养温度30°C,摇床转速160r/min,最佳碳源和氮源分别为葡萄糖和蛋白胨。最适培养条件下,所产絮凝剂对高岭土悬浮液的絮凝活性达到90.56%。     

Sphingomonas sp. X20絮凝特性及培养条件研究

目的:对分离筛选获得絮凝剂产生菌Sphingomonas sp.X20絮凝特性及培养条件进行研究.方法:采用单因素和正交实验确定最适产絮凝剂培养条件.结果:研究发现,菌株X20的微生物絮凝剂对高岭土悬液具有良好的絮凝效果,在温度为37℃、培养基初始pH7.0、摇床转速为100r/min条件下培养12h获得的絮凝剂絮凝活性最好,絮凝率达92.8%.正交实验结果表明,菌株Sphingomonas sp.X20产絮凝剂最佳培养基的组成:淀粉15g/L,NH4Cl 1.Og/L,KH2P04,2g/L,K2HP04 5g/L,NaC1 O.lg/L,MgS04·7H2O 0.2g/L,pH7.0.结论:菌株X20是一株高效的产絮凝剂菌,具有很好的应用前景.     

微生物絮凝剂产生菌的筛选及培养研究

从活性污泥中筛选出3株能产生高效絮凝活性的微生物,对其中1株TJ3进行其最佳培养条件及废水絮凝实验研究。结果表明TJ3的最佳培养条件为：以葡萄糖、蛋白胨作碳,氮源,初始pH值6～7,温度25～30℃,摇床转速120～160r/min,培养时间72h,可产生高絮凝活性的絮凝剂,对高岭土悬浊液絮凝率达92.4%,同时在最佳培养条件下,该菌所产絮凝剂对多种废水净化效果明显,尤其对净化分散兰染液,酵母菌菌液分离最为突出,絮凝率均在95%以上,具有较高的絮凝性能。     

一株絮凝菌的鉴定、絮凝基因定位及其絮凝剂成分分析

从武汉市综合废水处理的活性污泥中筛选得到一株絮凝剂产生菌株MBF03,其絮凝率达到90％以上,絮凝效果稳定.通过16S rDNA鉴定,该菌为泛菌属,扫描电镜结果显示为杆状.通过质粒转化与质粒消除试验,初步证实了MBF03菌的絮凝基因位于染色体上.提取该菌所产的絮凝剂,进行紫外、红外分析,结果表明,该絮凝剂主要成分是胞外多糖类物质,不含蛋白质和核酸.     

絮凝剂产生菌培养条件的研究及在废水处理中的应用

通过菌种富集、分离、纯化,从含有大量微生物菌群的土壤和活性污泥中筛选到一株对高岭土悬浊液具有较高絮凝活性的絮凝剂产生菌,将其命名为B23.通过研究该菌株在不同培养时间的生长情况和发酵液的絮凝活性,从而得出发酵液絮凝活性与菌体生长量呈正相关.通过对该菌株培养条件的研究表明,在培养时间为24h、培养温度为30℃、培养基初始pH值为8.0,以葡萄糖为碳源、(NH4)2SO4为氮源时,发酵液絮凝活性最强.用B23菌株所产絮凝剂处理废水后,废水中CODCr的去除率为62.48%,SS的去除率为84.47%,表明该菌株有良好的实际应用前景.     

一株产絮凝剂芽孢杆菌的分离及成份分析

从超高压灭菌的哈密瓜汁中筛选出一株具有高絮凝活性的芽孢杆菌。经形态及生理生化指标测试,初步确定该菌株为Bacillussp.B53。对此菌产生的絮凝活性成分纯化后经高效液相色谱、薄层层析分析表明该絮凝活性物质是聚γ谷氨酸,产量达到12.48g/L,该物质仅由谷氨酸组成,在212nm处有最大吸收峰,电泳结果表明Bacillussp.B53所产聚γ谷氨酸是分子量集中在440～669kD之间的多分子量聚集体,该絮凝剂有效地絮凝各种无机和有机的介质,高岭土和Ca(OH)2效果明显。     

Characteristics of a biopolymer flocculant produced by Bacillus sp. PY-90

A biopolymer flocculant-producing bacterium, strain PY-90, was isolated and considered to belong to Bacillus subtilis. For the production of biopolymer flocculant by strain PY-90, a medium containing 2 to 5% l-glutamic acid as a nitrogen source was suitable. The biopolymer flocculant was a homopolymer composed of glutamic acid residues and was presumed to be poly(γ-glutamic acid). In kaolin suspension, the highest flocculating activity was attained at the biopolymer flocculant concentration of 20 mg/l. The flocculating activity was increased by the addition of Ca²⁺, and the optimum concentration of which was about 2 to 8 mM. The flocculating activity was high in an acidic pH range of 3.0 to 5.0, and decreased upon heating at 100°C.     

Poly‐γ‐glutamic acid produced from Bacillus licheniformis CGMCC 2876 as a potential substitute for polyacrylamide in the sugarcane industry

As an environmentally friendly and industrially useful biopolymer, poly‐γ‐glutamic acid (γ‐PGA) from Bacillus licheniformis CGMCC 2876 was characterized by the high‐resolution mass spectrometry and ¹H NMR. A flocculating activity of 11,474.47 U mL^?1 obtained with γ‐PGA, and the effects of carbon sources, ions, and chemical properties (D‐/L‐composition and molecular weight) on the production and flocculating activity of γ‐PGA were discussed. Being a bioflocculant in the sugar refinery process, the color and turbidity of the sugarcane juice was IU 1,877.36 and IU 341.41 with 0.8 ppm of γ‐PGA, respectively, which was as good as the most widely used chemically synthesized flocculant in the sugarcane industry—polyacrylamide with 1 ppm. The γ‐PGA produced from B. licheniformis CGMCC 2876 could be a promising alternate of chemically synthesized flocculants in the sugarcane industry. © 2015 American Institute of Chemical Engineers Biotechnol. Prog., 31:1287–1294, 2015     

A novel flocculant biopolymer produced by Pestalotiopsis sp. KCTC 8637P

Summary A white rot fungus was isolated from rotted leaves and identified as Pestalotiopsis sp. KCTC 8637P. It produced a flocculant biopolymer. A flocculant was partially purified from the culture broth by series of precipitations with 95% ethanol and named as Pestan. The components of Pestan were consisted of glucose : glucosamine : glucuronic acid : rhamnose with a approximately molar ratio of 100:3.5:1.6:1.3.In kaolin suspension(final concentration was 4,800 mg/l), the highest flocculating activity was attained at the biopolymer flocculant concentration of 1 mg/l . The flocculating activity was observed most highest by the addition of cationic solutions, especially 8mM CaCl₂ · 2H₂O or 8mM FeCl₃. The thermal stability of Pestan was sustained up to 70 °C.     

Characterization and flocculation properties of biopolymeric flocculant (glycosaminoglycan) produced by Cellulomonas sp. Okoh

Aims

Bioflocculant production potential of an actinobacteria isolated from a freshwater environment was evaluated and the bioflocculant characterized.

Methods and Results

16S rDNA nucleotide sequence and BLAST analysis was used to identify the actinobacteria and fermentation conditions, and nutritional requirements were evaluated for optimal bioflocculant production. Chemical analyses, FTIR, 1H NMR spectrometry and SEM imaging of the purified bioflocculant were carried out. The 16S rDNA nucleotide sequences showed 93% similarities to three Cellulomonas species (strain 794, Cellulomonas flavigena DSM 20109 and Cellulomonas flavigena NCIMB 8073), and the sequences was deposited in GenBank as Cellulomonas sp. Okoh (accession number HQ537132 ). Bioflocculant was optimally produced at an initial pH 7, incubation temperature 30°C, agitation speed of 160 rpm and an inoculum size of 2% (vol/vol) of cell density 1·5 × 10⁸ cfu ml^?1. Glucose (88·09% flocculating activity; yield: 4·04 ± 0·33 g l^?1), (NH₄)₂NO₃ (82·74% flocculating activity; yield: 4·47 ± 0·55 g l^?1) and MgCl₂ (90·40% flocculating activity; yield: 4·41 g l^?1) were the preferred nutritional source. Bioflocculant chemical analyses showed carbohydrate, protein and uronic acids in the proportion of 28·9, 19·3 and 18·7% in CPB and 31·4, 18·7 and 32·1% in PPB, respectively. FTIR and 1H NMR indicated the presence of carboxyl, hydroxyl and amino groups amongst others typical of glycosaminoglycan. SEM imaging revealed horizontal pleats of membranous sheets closely packed.

Conclusion

Cellulomonas sp. produces bioflocculant predominantly composed of glycosaminoglycan polysaccharides with high flocculation activity.

Significance and Impact of the Study

High flocculation activity suggests suitability for industrial applications; hence, it may serve to replace the hazardous flocculant used in water treatment.     

一株产絮凝剂不动杆菌的筛选及其絮凝特性

从活性污泥中筛选出一株高效的微生物絮凝剂产生菌, 鉴定为鲍曼不动杆菌。蚕豆根尖细胞微核试验未显示该菌株所产絮凝剂具有遗传毒性。该菌产絮凝剂的最佳碳源和氮源分别为葡萄糖和酵母浸出汁, 培养时间为24 h。在絮凝体系中加入Ca2+能明显提高发酵液的絮凝率。在pH为8.0时对高岭土悬浊液和污水具有良好的絮凝效果。     

一株产絮凝剂不动杆菌的筛选及其絮凝特性

从活性污泥中筛选出一株高效的微生物絮凝剂产生菌,鉴定为鲍曼不动杆菌.蚕豆根尖细胞微核试验未显示该菌株所产絮凝剂具有遗传毒性.该菌产絮凝剂的最佳碳源和氮源分别为葡萄糖和酵母浸出汁,培养时间为24 h.在絮凝体系中加入Ca2 能明显提高发酵液的絮凝率.在pH为8.0时对高岭土悬浊液和污水具有良好的絮凝效果.     

Production of an exopolysaccharide bioflocculant by Sorangium cellulosum

AIMS: To isolate a new exopolysaccharide bioflocculant produced by the myxobacterium Sorangium cellulosum NUST06, and to characterize its chemical composition and expolysaccharide production relative to carbon source. METHODS AND RESULTS: Exopolysaccharide levels and biomass production by S. cellulosum NUST06 were analysed relative to carbon source. Glucose in the medium at a level of 3 g l(-1) completely inhibited cell growth and exopolysaccharide production, but low concentrations of glucose (1-2 g l(-1)) could stimulate cell utilization of starch. The chemical composition and flocculating activity of the NUST06 exopolysaccharide was investigated. The flocculant comprised 38.3% proteins and 58.5% carbohydrates, of which glucose, mannose and glucuronic acid were present at 51.3%, 39.2% and 10.5%, respectively. The flocculating activity of the NUST06 flocculant depended strongly on cations. CONCLUSIONS: It is feasible to produce an exopolysaccharide bioflocculant by the strain NUST06 in a mineral salts medium using starch as a carbon source. SIGNIFICANCE AND IMPACT OF THE STUDY: This strain may be advantageous for commercial bioflocculant production and may enrich existing knowledge of myxobacteria.     

The flocculation of bacteria using cationic synthetic flocculants and chitosan

Summary Bacteria are flocculated with high molecular weight cationic synthetic flocculants and chitosan. High charge density polymers are the most effective of the synthetic flocculants. Only chitosan is effective in flocculating the E. coli and B. subtilis cultures in complex broth. The difference in effectiveness between the synthetic flocculants and chitosan for flocculating E. coli, B. subtilis and Z. mobilis may be attributed to hydrogen bonding between the polysaccharide flocculant and cell surface polymers in addition to electrostatic interactions, and, in complex media, complexation of synthetic polymers with anionic polyelectrolytes.