产生5—氨基乙酰丙酸（ALA）光合细菌生物学研究进展

５－氨基乙酰丙酸（ＡＬＡ）是卟啉、血红素和维生素Ｂ１２４的类似物。ＡＬＡ作为一种无公害绿色除草剂、杀虫剂、抗微生物药剂、植物生长促进剂及治疗癌症与其它疾病等而备受国外研究者及产业界的关注。本文对ＡＬＡ光合细菌合成、调节途径、分子遗传学的研究作一简要综述。     

提高类球红细菌5-氨基乙酰丙酸产率的措施

5-氨基乙酰丙酸是四吡咯化合物生物合成的必需前体物,它作为一种无公害的绿色除草剂、杀虫剂、植物生长促进剂以及治疗癌症的药物而受到广泛的关注。文章综述了类球红细菌5-氨基乙酰丙酸的发酵生产现状以及提高其发酵产率的策略与措施。     

外源5-氨基乙酰丙酸对NaCl胁迫下酸枣光合特性的影响

以2年生酸枣幼苗为试验材料,探讨不同浓度NaCl(0、4、8、12g·kg-1)胁迫下喷施5-氨基乙酰丙酸(ALA,75、150mg·L~(-1))对酸枣光合特性的影响。结果显示:(1)不同浓度NaCl胁迫下,外源ALA对酸枣叶片的净光合速率(Pn)、胞间二氧化碳浓度(Ci)、气孔导度(Gs)、蒸腾速率(Tr)及叶绿素含量等具有明显促进作用。(2)在不同浓度NaCl胁迫下,喷施75mg·L~(-1)的ALA仅在NaCl浓度为4和8g·kg-1处理下对酸枣Tr值具有显著提高作用,而喷施150mg·L~(-1) ALA在各NaCl浓度胁迫下对其Pn、Ci和Tr均具有显著促进作用。(3)在重度NaCl胁迫(12g·kg-1)下,喷施150mg·L~(-1) ALA对酸枣叶片叶绿素含量具有显著提高作用,而喷施75mg·L~(-1)浓度ALA却无明显提高。研究表明,在NaCl胁迫条件下,外源ALA能有效改善酸枣叶片光合气体交换参数,提高叶绿素含量,从而缓解NaCl胁迫的伤害,提高其光合能力,并以喷施150mg·L~(-1) ALA的缓解效果更好。     

表达酿酒酵母ALAS的重组大肠杆菌胞外5-氨基乙酰丙酸的产量和纯化

5-氨基乙酰丙酸(5-aminolevulinate,ALA)由5-氨基乙酰丙酸合酶(5-aminolevulinate synthase,ALAS)催化产生。利用重组细菌在大肠杆菌合成ALA已有不少研究。重组真核生物ALAS在大肠杆菌合成ALA的研究没有报道。酿酒酵母ALAS在大肠杆菌重组表达,在摇瓶培养条件下,分析了胞外ALA的产量,重组菌的生长状况和细胞中ALAS的活性,利用两种国产树脂纯化ALA,毛细管电泳分析确定ALA纯度在LB培养基中,初始pH6.5,含有20mmol/L的酮戊酸、20mmol/L琥珀酸和20mmol/L的甘氨酸,37℃下诱导培养12h,胞外ALA的产量为162mg/L培养基。纯化的ALA纯度达到90%。     

表达浑球红细菌hemA基因生产5-氨基乙酰丙酸的研究

5-氨基乙酰丙酸（5-aminolevulinate acid,ALA）在农业,工业,医药业具有广泛的应用。ALA由5-氨基乙酰丙酸合酶（5-aminolevulinate acid synthase, ALAS）催化产生,其生物合成受终产物血红素的反馈抑制。本研究克隆一种浑球红细菌的hemA基因,序列分析其与已报道的基因具有96％的同源性,蛋白质编码区域也发生改变,并利用生物信息学软件进行同源关系的分析。采用大肠杆菌重组技术,构建表达载体pET28a—hemA,表达了有活性的浑球红细菌（Rhodobacter sphaeroides）的ALAS,研究了IPTG诱导和PH对研究ALAS的影响,同时分析了重组菌株合成ALA的能力,测定胞外产量。结果表明,在PH6．5,30mmol／L琥珀酸和60mmol／L甘氨酸培养条件下,胞外ALA的最大合成量达到669mg／L。     

微生物发酵生产5-氨基乙酰丙酸研究进展

5-氨基乙酰丙酸是生物体内吡咯生物合成途径的关键中间产物,具有广泛的应用前景。文中从三方面归纳了国内外关于5-氨基乙酰丙酸的最新研究进展:生产5-氨基乙酰丙酸的微生物筛选分离与诱变;基于C4途径的微生物全细胞生物转化合成5-氨基乙酰丙酸;基于微生物代谢工程改造构建高产5-氨基乙酰丙酸的工程菌株。最后,预测了未来5-氨基乙酰丙酸的研究方向和焦点。     

5-氨基乙酰丙酸对喜树幼苗盐害缓解的生理机制研究

为明确5-氨基乙酰丙酸(ALA)的生理生化机理,研究了ALA对喜树幼苗盐害的缓解效应。结果表明,80 mg L~(–1)的ALA对喜树幼苗盐胁迫的缓解效果更佳。80mgL~(–1)的ALA处理提升了盐胁迫下喜树幼苗的抗氧化能力,显著增加了幼苗叶片的氮素含量和叶绿素含量,缓解了盐胁迫对PSⅡ的破坏,提高了光合碳同化能力,从而促进幼苗生长。盐胁迫下喜树幼苗叶片的过氧化物酶(POD)活性和叶绿素含量并未随ALA浓度增加而升高。这为喜树的抗盐栽培提供了理论依据。     

5-氨基乙酰丙酸对秋冬季大棚西瓜叶片光合作用及抗氧化酶活性的影响

以秋冬季塑料大棚中盆栽西瓜幼苗为材料,研究了50~200 mg/L 5-氨基乙酰丙酸(ALA)处理对低温弱光条件下西瓜植株光合特性、碳水化合物积累、抗氧化酶活性和丙二醛(MDA)含量的影响。结果表明,外源ALA处理显著提高了西瓜幼苗叶片净光合速率(Pn)、气孔导度(Gs)和蒸腾速率(Tr)。ALA处理还显著提高了叶片SOD和POD等抗氧化酶活性,但对CAT及APX活性影响不大,暗示ALA处理可能主要通过提高植株SOD和POD活性来促进西瓜幼苗活性氧代谢,从而保护细胞光合性能。处理后30 d分析表明,ALA处理植株干物质重量比对照高出42%~54%,淀粉含量增加62.2%~207.0%,可溶性糖含量也增加32.0%~87.1%。以上结果说明,ALA处理可以增强低温弱光条件下西瓜幼苗抗氧化系统活性,促进光合作用与光合产物积累,并促进植株生长。     

5-氨基乙酰丙酸对NaCl胁迫下番茄幼苗光合特性的影响

为探讨5-氨基乙酰丙酸（ALA）对NaCl胁迫下番茄光合特性的调控作用,以‘金鹏一号’番茄幼苗为试材,研究叶面喷施50 mg·L^-1或根施10 mg·L^-1 ALA对100 mmol·L^-1 NaCl胁迫下番茄幼苗光合及叶绿素荧光参数的影响.结果表明： NaCl胁迫下,番茄幼苗光合气体交换参数（净光合速率P_n、气孔导度g_s、胞间CO₂浓度C_i、蒸腾速率T_r）及叶绿素荧光参数（实际光化学量子产量F_v′/F_m′、F_m′、PSⅡ反应中心实际光化学效率Φ_PSⅡ、表观光合电子传递效率ETR、光化学淬灭q_P、光化学反应Pc）均显著降低,根施或叶施ALA均可以提高NaCl胁迫下番茄叶片的光合能力,但两种处理方式之间存在一定差异.叶面喷施50 mg·L^-1ALA或根施10 mg·L^-1ALA处理均显著提高了番茄叶片P_n、T_r、g_s和C_i,提高了水分利用效率（WUE）,显著增加了NaCl胁迫下叶片的最大净光合速率,减轻了光抑制.根施ALA对叶绿素含量的作用效果较好,而叶施ALA对光合参数的作用效果较好,两处理叶绿素荧光参数差异不显著.叶面喷施或根施ALA可以提高番茄幼苗的耐盐性,其调控作用与促进叶绿素合成与稳定、维持正常气孔开闭、降低气孔限制,进而提高NaCl胁迫下番茄叶片的光合能力和PSⅡ光化学效率有关.
     

重组球形红细菌5-氨基乙酰丙酸合酶同工酶hemA和hemT的特性

将编码光合细菌Rhodobactersphaeroides 5- 氨基乙酰丙酸合酶(ALAS)的同工酶基因hemA、hemT转入E .coli中进行高表达,并将高表达的同工酶进行分离、纯化.纯化的hemA是可溶的,并具有催化活性,而hemT大部分是不溶的,且在体外条件下无活性.与其它重组ALAS相比,R .sphaeroides的hemA活性表达需PLP作为催化因子,除去PLP或用硼酸钠破坏与PLP的连接,hemA活性下降90 % .hemA PLP的紫外 可见光谱分析表明hemA与PLP之间形成一个醛亚胺键,而hemT与PLP之间未形成该键.hemA对修饰组氨酸、精氨酸、胱氨酸残基的试剂很敏感,对可切割Arg15 1和Ser15 2的类胰蛋白酶也很敏感,PLP也不能阻止该酶的切割作用.抗血清试验表明,hemA、hemT的抗血清均可与小鼠的ALAS杂交,并都有一个抗原决定簇.     

Utilization of volatile fatty acids from the anaerobic digestion liquor of sewage sludge for 5-aminolevulinic acid production by photosynthetic bacteria

Using volatile fatty acids (VFA) from the anaerobic digestion liquor of sewage sludge, up to 9.2 mm 5-aminolevulinic acid (ALA) could be produced by Rhodobacter sphaeroides under anaerobic-light (5 kLux) conditions with repeated addition of levulinic acid (LA) and glycine and using a large inoculum (approx. 2 g/l of cells, initially from glutamate/malate medium). As the VFA medium also contained organic nitrogen sources such as glutamic acid, the cells were later grown up to about 2 g/l in the VFA medium instead of the glutamate/malate medium. ALA production was then again promoted by adding LA and glycine. Using this improved method, up to 9.3 mm ALA was produced by feeding propionate and acetate together with LA and glycine, indicating that VFA medium formed from sewage sludge could be useful for ALA production.     

Production of 5-aminolevulinic acid by photosynthetic bacteria

Extracellular formation of 5-aminolevulinic acid (ALA) by adding levulinic acid (LA), an inhibitor of ALA dehydratase, was examined in the anaerobic-light culture of Rhodobacter sphaeroides. The addition of LA (10–25 mmol/l) during the middle log phase retarded the growth and accelerated the extracellular formation of ALA, while over 50 mmol/l completely suppressed both growth and formation.The formation of ALA was closely related to intracellular ALA synthetase activity. Light intensity was also an important factor for enhancing ALA formation. The optimal condition, addition of 15 mmol/l of LA during the middle log phase with 3 klx illumination, resulted in ALA formation of 0.26 mol/l. In addition, supplementation with glycine (30 mmol/l) and succinate (30 mmol/l), precursors of ALA biosynthesis, enhanced ALA formation up to ca. 2 mmol/l.     

Treatment of high strength organic wastewater by a mixed culture of photosynthetic microorganisms

The growth characteristics and nutrient removal fromsynthetic wastewater by Rhodobacter sphaeroides,Chlorella sorokiniana and Spirulinaplatensis were investigated under aerobic dark(heterotrophic) and aerobic light (photoheterotrophic)conditions. Both in terms of economy and efficiency,aerobic dark conditions were the best for wastewatertreatment using R. sphaeroides and C.sorokiniana, but light was necessary with S.platensis. Neither growth nor nutrient removalcharacteristics of the cells were affected insynthetic wastewater with as high as 10 000 ppmacetate, 1000 ppm propionate, 700 ppm nitrate and 100 ppmphosphate. Although R. sphaeroides and C. sorokiniana showed good growth in syntheticwastewater containing 400 ppm of ammonia, S.platensis was completely inhibited.When grown as a monoculture, none of thestrains could simultaneously remove acetate,propionate, ammonia, nitrate and phosphate from thewastewater. R. sphaeroides could remove allthe above nutrients except nitrate, but the rate of removal was relatively low. The rate of nutrientsremoval by C. sorokiniana was higher, but theorganism could not remove propionate; S.platensis could efficiently remove nitrate, ammoniaand phosphate, but none of the organic acids. A mixedculture of R. sphaeroides and C.sorokiniana was therefore used for simultaneousremoval of organic acids, nitrate, ammonia andphosphate. The optimum ratio of the cells depended onthe composition of the wastewater.     

Algal photosynthetic aeration increases the capacity of bacteria to degrade organics in wastewater

Wastewater treatment is an energy-intensive process and a net emitter of greenhouse gas emissions. A large fraction of these emissions is due to intensive aeration of aerobic bacteria to facilitate break-down of organic compounds. Algae can generate dissolved oxygen at levels in excess of saturation, and therefore hold the potential to partially displace or complement mechanical aeration in wastewater treatment processes. The objective of this study was to develop an internally consistent experimental and modeling approach to test the hypothesis that algal photosynthetic aeration can speed the removal of organic constituents by bacteria. This framework was developed using a simplified wastewater treatment process consisting of a model bacteria (Escherichia coli), a model algae (Auxenochlorella protothecoides), and a single carbon source that was consumable by bacteria only. This system was then tested both with and without the presence of algae. A MATLAB model that considered mass transfer and biological kinetics was used to estimate the production and consumption of O₂ and CO₂ by algae and bacteria. The results indicated that the presence of algae led to 18–66% faster removal of COD by bacteria, and that roughly one-third of biochemical oxygen demand was offset by algal photosynthetic aeration.     

微生物处理高盐工业有机废水工艺研究进展

随着我国工业化进程加快,其所造成的水污染现象也越来越严重。含盐有机废水的排放会导致环境进一步恶化,为了合理循环利用水资源,相关废水的有效处理至关重要。本文从微生物角度出发,通过典型案例阐述了目前基于微生物所运行的生物工艺技术在高含盐有机废水领域中的研究进展,综述了微生物在高盐环境中的生存与耐受机制,以及在处理高盐工业有机废水方面的研究与应用情况,进一步提出了目前存在的问题及未来在本领域研究与应用的展望,为高盐工业有机废水的生物处理发展方向提供一定的参考。     

Identification and cultivation of photosynthetic bacteria in wastewater from a concentrated latex processing factory

Ten strains of purple non-sulfur photosynthetic bacteria, isolated from wastewater produced by a concentrated latex processing factory, were cultivated in a wastewater medium without supplementation. After 40 h cultivation, one strain SS51, decreased the COD content of the wastewater by 34%. Optimal ratio of mixed-cultivation between SS51 and SY40 was 14:7 (ml/ml), and the COD content of the wastewater was decreased by 57%. Both strains were identified as Rubrivivax gelatinosus.     

固体发酵法固定工业废水处理优势菌的研究

为实现优势菌种的工程应用,由焦化废水处理站污泥筛选优势好氧菌A和兼性厌氧菌F,使用谷壳g、豆皮d为载体,采用固体发酵法进行固定化产品制备。初步研究表明固体发酵法固定菌种具有可行性,主要调控因素有温度、初始含水率、工业废水比例、pH、通风量和发酵时间。以pH8．0、温度好氧菌30℃（兼性厌氧菌35℃）、接种量1mL茴液儋田定化载体,初始含水量80％,固体发酵时间5d,低于60℃鼓风干燥,制备固定化产品。保存三个月,谷壳固定化产品好氧菌八的硝化能力和兼性厌氧菌R的反硝化能力不随保存时间的延长而改变;豆皮固定化产品氏、Fd降解能力随保存时问延长下降12％左右。以实验室岔／O工艺系统验证固定化产品处理焦化废水效果,缺氧池中无NO3-N积累,反硝化作用明显。氐和气对氰化物的去除率均达99％以上;对苯酚的去除效果气（98．84％）优于氏（79．6％）;但对NH4＋-N的去除率氏（75．46％）优于Ag（62．55％）。     

Use of wood vinegar to enhance 5-aminolevulinic acid production by selected Rhodopseudomonas palustris in rubber sheet wastewater for agricultural use

This study aimed to produce inexpensive 5-aminolevulinic acid (ALA) in a non-sterile latex rubber sheet wastewater (RSW) by Rhodopseudomonas palustris TN114 and PP803 for the possibility to use in agricultural purposes by investigating the optimum conditions, and applying of wood vinegar (WV) as an economical source of levulinic acid to enhance ALA content. The Box–Behnken Design experiment was conducted under microaerobic-light conditions for 96 h with TN114, PP803 and their mixed culture (1:1) by varying initial pH, inoculum size (% v/v) and initial chemical oxygen demand (COD, mg/L). Results showed that the optimal condition (pH, % inoculum size, COD) of each set to produce extracellular ALA was found at 7.50, 6.00, 2000 for TN114; 7.50, 7.00, 3000 for PP803; and 7.50, 6.00, 4000 for a mixed culture; and each set achieved COD reduction as high as 63%, 71% and 75%, respectively. Addition of the optimal concentration of WV at mid log phase at 0.63% for TN114, and 1.25% for PP803 and the mixed culture significantly increased the ALA content by 3.7–4.2 times (128, 90 and 131 μM, respectively) compared to their controls. ALA production cost could be reduced approximately 31 times with WV on the basis of the amount of levulinic acid used. Effluent containing ALA for using in agriculture could be achieved by treating the RSW with the selected ALA producer R. palustris strains under the optimized condition with a little WV additive.     

Isolation,identification and growth conditions of photosynthetic bacteria found in seafood processing wastewater

Four photosynthetic bacteria, isolated from 14 samples taken from seafood processing plants, were identified as species of Rhodocyclus gelatinosus, belonging to the purple, non-sulphur bacteria of the family Rhodospirillaceae. Cultivation in synthetic medium under four different conditions indicated that all four strains gave maximum carotenoid and bacteriochlorophyll synthesis under anaerobic conditions in the light, with values of 11 to 12.6 and 102 to 108 mg/g dry cell wt, respectively. These values are 87% higher than the pigment content obtained from aerobic cultivation, although the cell biomass of all strains (1.7 to 2.3 g/l) was 22 to 38% higher under aerobic conditions. Protein content was always between 32 and 43%. The specific growth rates of all isolates in aerobic cultivation (0.04 to 0.06 h^-1) were twice those in anaerobic conditions in the light. No growth occurred in anaerobic conditions in the dark.