固定化微生物对水胺硫磷降解活性评价指标的研究

对水胺硫磷水样在生物降解前后的性能评价指标进行了研究,结果表明,有机磷,农药含量及降解率与ＣＯＤＣＲ及其去除率分别呈高度正相关,因此,选用ＣＯＤＣＲ去除率作为固定化微生物对农药降解活性的常用评价指标是适宜的。文中还给出由试验数据的回归方程及其显著检验结果。     

光合细菌与酵母跨界融合子降解味精废水性能测定

为了筛选出能综合双亲优势的杂种细胞,为废资源化生产ＳＣＰ提供更为理想的菌株来源,将原核球形红假单胞菌细胞与真核酿酒酵母细胞的原生质体融合,构建成跨界杂种细胞。从中筛选出Ｆ１３,Ｆ１５,Ｆ２０三株高絮凝性融合细胞,在起始ＢＯＤ５浓度为１９１－６９０ｍｇ／Ｌ,ｐＨ７．０,３０℃的味精废水中振荡反应７－８ｈ测得融合细胞双亲菌株降解利用有机污染物的系列的反应动力学参数μｍａｘ,ｑｍａｘ,Ｋｓμ,Ｋｓｑ,Ｙ     

细菌降解非离子表面活性剂的研究

从石油污染的土壤中分离到２株能利用非离子表面活性剂ＡＥＯ－９和ＳＡ－２０作为唯一碳源生长的细菌。这２株菌被定名为假单胞杆菌５２（Ｐｓｅｕｄｏｍｏｎｏｓ５２）和Ｗｅｅｋｓｅｌｌａ６．最适于这２株菌利用非离子表活剂ＡＥＯ－９的培养条件是乙酸胺作为氮源,ｐＨ７．３０℃添加少量葡萄糖促进表活性的降解,降解速率的研究表明,当ＡＥＯ－９的初始浓度为５０００ｍｇ／Ｌ时,５２号菌和６号菌能在２周内将其去除８５％,     

睾丸酮丛毛单胞菌对喹啉类化合物的降解

对喹啉、异喹啉、2-甲基喹啉、3-甲基喹啉、4-甲基喹啉和6-甲基喹啉在睾丸酮丝毛单胞菌(Comamonas testosteroni Q10)作用下的降解及底物之间的相互作用进行研究．结果表明,喹啉和3-甲基喹啉不仅能有效地被降解,而且细菌也有明显的生长,而其它化合物虽有部分降解但没有观察到细胞生长．底物初始浓度的增加对菌Q10有一定抑制作用．喹啉的存在对其它化合物的降解具有不同的促进效应,其中尤以6-甲基喹啉和4-甲基喹啉最为明显．能在较短时间内得到完全去除,而在各二元体系中喹啉的降解受到这些化合物的抑制作用．     

两株联合降解甲基一六○五菌的分离及其特性研究

从农药厂污泥中分离得到一个降解甲基一六○五的混合菌群,该菌群由两种菌 Ｍ６ 和 Ｐ３ 组成,初步鉴定均为假单胞菌属（ ｐｓｅｕｄｍｏｎａｓ ．ｓｐ） ． Ｍ６ 菌具有一硫代磷酸酯键水解酶,能够催化甲基一六○五水解为对硝基酚, Ｐ３ 具有对硝基酚降解能力． Ｍ６ 和 Ｐ３ 各自均不能彻底矿化甲基一六○五． Ｍ６ 与 Ｐ３ 混和可以彻底降解甲基一六○五．质粒消除实验表明, Ｓ Ｄ Ｓ、吖啶橙（ Ｏ Ａ） 、丝裂霉素及几种消除剂混和处理均不能使 Ｍ６ 和 Ｐ３ 丧失一六○五水解和对硝基酚降解能力,质粒检测发现在 Ｍ６ 中检测到质粒条带,而 Ｐ３ 中未检测到质粒条带     

红球菌Chr-9降解吡啶和苯酚的特性

研究了红球菌(Rhodococcus)Chr-9菌株在基础盐培养基中降解吡啶和苯酚的特性,分析了菌株降解苯酚和吡啶间的差异.结果表明,菌株Chr-9能够在72 h内将基础盐培养基中的吡啶(200 mg L-1)和苯酚(200 mg L-1)完全降解,同时利用吡啶和苯酚进行生长.菌株降解吡啶的最适温度为35℃,最适pH为8.0.菌株降解吡啶和苯酚的速度与底物的初始浓度呈负相关;在无其它氮源的基础盐培养基中,菌株能够利用吡啶和苯酚协同生长.图7参12     

Biodegradation and bioconversion of cellulose wastes using bacterial and fungal cells immobilized in radiopolymerized hydrogels

Annually, great amounts of cellulose wastes, which could be measured in many billions of tons, are produced worldwide as residues from agricultural activities and industrial food processing. Consequently, the use of microorganisms in order to remove, reduce or ameliorate these potential polluting materials is a real environmental challenge, which could be solved by a focused research concerning efficient methods applied in biological degradation processes. In this respect, the scope of this chapter is to present the state of the art concerning the biodegradation of redundant cellulose wastes from agriculture and food processing by continuous enzymatic activities of immobilized bacterial and fungal cells as improved biotechnological tools and, also, to report on our recent research concerning cellulose wastes biocomposting to produce natural organic fertilizers and, respectively, cellulose bioconversion into useful products, such as: ‘single-cell protein’ (SCP) or ‘protein-rich feed’ (PRF). In addition, there are shown some new methods to immobilize microorganisms on polymeric hydrogels such as: poly-acrylamide (PAA), collagen-poly-acrylamide (CPAA), elastin-poly-acrylamide (EPAA), gelatin-poly-acrylamide (GPAA), and poly-hydroxy-ethyl-methacrylate (PHEMA), which were achieved by gamma polymerization techniques. Unlike many other biodegradation processes, these methods were performed to preserve the whole viability of fungal and bacterial cells during long term bioprocesses and their efficiency of metabolic activities. The immobilization methods of viable microorganisms were achieved by cellular adherence mechanisms inside hydrogels used as immobilization matrices which control cellular growth by: reticulation size, porosity degree, hydration rate in different colloidal solutions, organic and inorganic compounds, etc. The preparative procedures applied to immobilize bacterial and fungal viable cells in or on radiopolymerized hydrogels and, also, their use in cellulose wastes biodegradation are discussed in detail. In all such performed experiments were used pure cell cultures of the following cellulolytic microorganisms: Bacillus subtilis and Bacillus licheniformis from bacteria, and Pleurotus ostreatus, Pleurotus florida, and Trichoderma viride from fungi. These species of microorganisms were isolated from natural habitats, then purified by microbiological methods, and finally, tested for their cellulolytic potential. The cellulose biodegradation, induced especially by fungal cultures, used as immobilized cells in continuous systems, was investigated by enzymatic assays and the bioconversion into protein-rich biomass was determined by mycelial protein content, during such long time processes. The specific changes in cellular development of immobilized bacterial and fungal cells in PAA hydrogels emphasize the importance of physical structure and chemical properties of such polymeric matrices used for efficient preservation of their metabolic activity, especially to perform in situ environmental applications involving cellulose biodegradation by using immobilized microorganisms as long-term viable biocatalysts.     

邻苯二甲酸二丁酯的微生物降解

通过驯化富集培养,从处理石化厂废水的活性污泥中分离出１株邻苯二甲酸酯降解菌ＦＳＩ,研究了邻苯二甲酸酯菌ＦＳＩ对邻苯二甲酸二丁酯的生物降解特性。邻苯二甲酸酯降解菌ＦＳＩ降解最适酸度为ｐＨ６．５～８．０,温度为２０～３５℃。菌株ＦＳＩ对邻苯二甲酸二丁酯的生物降解反应速率遵循一级反应动力学模式。试验结果表明,菌株ＦＳＩ对邻苯二甲本二丁酯具有高效降解作用。     

甲胺磷降解真菌的研究

从受甲胺磷长期污染的土壤样品中通过富集培养,亚硝基胍（ＮＴＧ）诱变处理,从中分离筛选到一株降解甲胺磷活性较高的Ｌ４８菌株。该菌株可以利用甲胺磷作为碳源和能源而生长,降解甲胺磷的最适温度为３０℃,最适宜ＰＨ值为７．０,其完整细胞悬液对３０００ｍｇ／Ｌ左右甲胺磷的降解率最高可达８３％。经初步鉴定该菌株为华丽曲霉Ａｓｐｅｒｇｉｌｌｕｓ．ｏｒａｎｔｕｓ。     

降解微囊藻毒素菌种的筛选和活性研究

研究了滇池底泥和表层水体中的微生物菌群降解微囊藻毒素(Microcystins, MCs)的能力差异,发现底泥中的微生物菌群对MCs有更强的生物降解能力.采用从滇池水华蓝藻细胞中提取提纯的微囊藻毒素作为微生物生长的唯一碳源和氮源,先后经过液体和固体培养基培养后,通过挑取单克隆菌落,分别从底泥中筛选出了能够降解MC-RR和LR的5种不同微生物菌种.其中筛选的菌种D降解MCs的能力最强,在3 d内可将初始浓度分别为60.1 mg·L^-1和38.7 mg·L^-1的MC-RR和LR全部降解,日均降解MC-RR和LR的速率分别高达20.0 mg·L^-1和12.9 mg·L^-1.