用b-紫罗兰酮筛选虾青素高产菌株

用β-紫罗兰酮作为筛选剂选择性分离海洋红酵母虾青素高产突变菌株。实验结果表明, 在β-紫罗兰酮存在的情况下, 由于类胡萝卜素合成受到抑制, 海洋红酵母的生物量和虾青素合成量都减少; 当平板培养基中β-紫罗兰酮浓度达到370 mg/L时, 海洋红酵母的致死率为92.3%; 在这种平板培养基上涂布经甲基磺酸乙酯诱变的海洋红酵母, 随机筛选200个菌落, 结果表明生物量、虾青素体积产率和细胞产率均有所提高的正突变株占18%, 生物量、虾青素体积产率和细胞产率的单项指标有所提高的正突变株分别占22.5%、45%和46%。该实验结果表明在分离培养基中添加β-紫罗兰酮可选择性地分离海洋红酵母虾青素高产菌株, 提高虾青素高产突变株的筛选效率。     

用β-紫罗兰酮筛选虾青素高产菌株

用β-紫罗兰酮作为筛选剂选择性分离海洋红酵母虾青素高产突变菌株.实验结果表明,在β-紫罗兰酮存在的情况下,由于类胡萝卜素合成受到抑制,海洋红酵母的生物量和虾青素合成量都减少;当平板培养基中β-紫罗兰酮浓度达到370 mg/L时,海洋红酵母的致死率为92.3%:在这种平板培养基上涂布经甲基磺酸乙酯诱变的海洋红酵母,随机筛选200个菌落,结果表明生物量、虾青素体积产率和细胞产率均有所提高的正突变株占18%,生物量、虾青素体积产率和细胞产率的单项指标有所提高的正突变株分别占22.5%、45%和46%.该实验结果表明在分离培养基中添加β-紫罗兰酮可选择性地分离海洋红酵母虾青素高产菌株,提高虾青素高产突变株的筛选效率.     

法夫酵母PLX-All发酵纤维素酶水解物合成虾青素*

法夫酵母（Phaffia rhodozyma)PLX-All菌株能够发酵纤维素酶水解物进行虾青素的生物合成。纤维素的酶解物主要为纤维二糖和葡萄糖,在另外添加适量其它营养物后可被法夫酵母发酵用于生长及合成虾青素。摇瓶试验结果表明,培养108h,法夫酵母的生物量可达2.3g／L,虾青素的产率达913.4g／g干细胞,虾青素体积产率为2.1mg／L。在2L罐的发酵试验中,法夫酵母的生物量可达3.23g／L（第96h）,虾青素的产率达581.4g／g干细胞,虾青素体积产率达1.88mg／L。     

法夫酵母PLX-All发酵纤维素酶水解物合成虾青素

法夫酵母（Phaffia rhodozyma)PLX-All菌株能够发酵纤维素酶水解物进行虾青素的生物合成。纤维素的酶解物主要为纤维二糖和葡萄糖,在另外添加适量其它营养物后可被法夫酵母发酵用于生长及合成虾青素。摇瓶试验结果表明,培养108h,法夫酵母的生物量可达2.3g／L,虾青素的产率达913.4g／g干细胞,虾青素体积产率为2.1mg／L。在2L罐的发酵试验中,法夫酵母的生物量可达3.23g／L（第96h）,虾青素的产率达581.4g／g干细胞,虾青素体积产率达1.88mg／L。     

法夫酵母PLX-ll发酵纤维素酶水解物合成虾青素

法夫酵母（Phaffiarhodozyma)PLX朅ll菌株能够发酵纤维素酶水解物进行虾青素的生物合成。纤维素的酶解物主要为纤维二糖和葡萄糖,在另外添加适量其它营养物后可被法夫酵母发酵用于生长及合成虾青素。摇瓶试验结果表明,培养108h,法夫酵母的生物量可达2.3g／L,虾青素的产率达913.4g／g干细胞,虾青素体积产率为2.1mg／L。在2L罐的发酵试验中,法夫酵母的生物量可达3.23g／L（第96h）,虾青素的产率达581.4g／g干细胞,虾青素体积产率达1.88mg／L。     

用Cu^2＋筛选虾青素高产菌株的研究

海洋红酵母经过甲基磺酸乙酯诱变,以500μmol/L浓度的Cu2 为筛选剂,随机挑取200株菌株,其中细胞生物量、虾青素细胞产率和体积产率都增加的有38株,正突变率为19%。实验结果表明,Cu2 可以作为虾青素高产菌株的筛选剂。     

法夫酵母PLX—A11发酵纤维素酶水解物合成虾青素

法夫酵母（Ｐｈａｆｆｉａ ｒｈｏｄｏｚｙｍａ）ＰＬＸ－Ａ１１菌株能够发酵纤维素酶水解物进行虾青素的生物合成。纤维素的酶解物主要为纤维二糖和葡萄糖,在另外添加适量其它营养物后可被法夫酵母发酵用于生长及俣成虾青素。摇瓶试验结果表明,培养１０８ｈ,法夫酵母的生物量可达２．３ｇ／Ｌ,虾青素的产率达９１３．４μｇ／ｇ干细胞,虾青素体积产率为２．１ｍｇ／Ｌ。在２Ｌ罐的发酵试验中,法夫酵母的生物量可达３．２３ｇ     

法夫酵母产虾青素的反复分批及反复分批补料发酵

以生物量和虾青素产量为指标,考察法夫酵母多批次半连续培养产虾青素的稳定性。实验结果显示,在摇瓶上分别以4 d和5 d为周期反复分批培养法夫酵母,虾青素产量呈现先增加再下降的趋势,但第2代至第7代虾青素产量仍高于第1代,并且4 d为周期的虾青素平均产量略高于5 d的。在5 L罐法夫酵母进行反复分批补料发酵中,不管是补加30％的葡萄糖还是补加30％的淀粉水解糖,第2个批次发酵的生物量和虾青素产量均达到第1个批次的水平,表明菌种稳定性较好。     

氧载体强化氧传递促进法夫酵母虾青素的合成*

法夫酵母生物合成虾青素是强好氧发酵过程,溶氧水平直接影响细胞虾青素的产率。本文对虾青素的氧载体强化氧传递双液相发酵进行了研究。实验结果表明,添加豆油(作为氧载体)可提高法夫酵母发酵时的溶氧水平,促进虾青素的合成:添加豆油 0.5-5.0%(w/v),虾青素产量随豆油添加量逐步提高,最高时达到2.98mg/L,对照组虾青素产率为2.50mg/L。并证明产量的提高是单位质量细胞的虾青素合成效率提高的结果。摇瓶培养时转速的高低不同,对豆油的最适添加量存在影响。较高摇瓶转速有利于豆油在培养基中分散,从而利于强化氧的传递。     

氧载体强化氧传递促进法夫酵母虾青素的合成

法夫酵母生物合成虾青素是强好氧发酵过程,溶氧水平直接影响细胞虾青素的产率。本文对虾青素的氧载体强化氧传递双液相发酵进行了研究。实验结果表明,添加豆油(作为氧载体)可提高法夫酵母发酵时的溶氧水平,促进虾青素的合成：添加豆油 0.5-5.0％ (w／v),虾青素产量随豆油添加量逐步提高,最高时达到 2.98mg/L,对照组虾青素产率为 2.50mg/L。并证明产量的提高是单位质量细胞的虾青素合成效率提高的结果。摇瓶培养时转速的高低不同,对豆油的最适添加量存在影响。较高摇瓶转速有利于豆油在培养基中分散,从而利于强化氧的传递。     

Evaluation of changes in the element content and biomass of invaded with Meloidogyne arenaria Tiny Tim tomato plants under NH4VO3 treatment

The parasite-host system Meloidogyne arenaria--Tiny Tim tomato plants has been studied in order to investigate the influence of the process of invasion on the chemical composition and biomass of plants. The concentrations of seven chemical elements Cu, Zn, Mg, K, Na, Mn and Fe have been determined using AAS in controls and invaded plants, and their changes have been evaluated under treatment with NH4VO3 in three different concentrations 0.01, 0.1 and 0.13 mg/100 ml H2O. The process of treatment with NH4VO3 disbalances significantly the trace element content of plants. The lowest concentration (0.01 mg NH4VO3) causes bigger changes in the concentrations of Mn, Fe and Na in non-invaded plants. The highest concentration (0.13 mg NH4VO3) balances the content of the elements back to their levels in the control plants for the elements Zn, Fe and Na. The pure effect of the process of invasion with Meloidogyne arenaria on the biomass (leaves, stems, roots and total biomass) of Tiny Tim plants is expressed in a significant increasing, mainly due to the development of the parasites. After treatment with different concentrations of NH4VO3 the decreasing in the biomass of leaves, stems and roots is observed which reflects on the total biomass of plants. The concentration of NH4VO3 eliminates the unfavourable changes not only in the chemical content of plants but also in their biomass. It could be taken into consideration as an alternative method used instead of treatment with nematocides.     

金属离子对粪产碱杆菌C16的脱氮和亚硝酸盐积累的影响

【目的】研究不同金属离子对异养氨氧化细菌C16的生长和脱氮性能影响,探讨适于C16生长和脱氮的金属离子及其浓度。【方法】实验选用Mg2+、Mn2+、Fe2+、Cu2+、Zn2+5种金属离子,对C16的生长﹑脱氮性能﹑亚硝酸盐氮积累以及相关酶活性进行研究。【结果】Mg2+明显促进C16的生长和NH4+-N氧化速率;较高浓度Mn2+使得C16无法生长;原培养基中缺少Fe2+会抑制C16的生长和NH4+-N氧化速率;在原培养基中加入0.1 mmol/L的Cu2+对C16的生长和脱氮具有一定的促进作用,Cu2+使得培养基中基本无NO2--N和NH2OH的积累;不同浓度的Zn2+对C16的生长和氨氮去除有抑制作用。酶活实验结果显示,0.1 mmol/L Mg2+促进了羟胺氧化还原酶(HAO)的活性;0.1 mmol/L Cu2+促进了硝酸盐还原酶(Nar)和亚硝酸盐还原酶(Nir)的活性。【结论】Mg2+是C16生长和脱氮过程中的一种重要金属离子;加入Cu2+可避免过量亚硝酸盐积累。     

Growth of Dalbergia sissoo in desert regions of western India using municipal effluent and the subsequent changes in soil and plant chemistry

Increasing demand for fodder and fuelwood and the scarcity of a good quality water in arid areas has resulted in a search for an alternative source of water for biomass production. An experiment utilizing municipal effluent in growing Dalbergia sissoo was conducted. Five treatments included T1, municipal effluent at 1 PET (Potential evapo-transpiration) (without plant); T2, municipal effluent at 1/2 PET; T3, municipal effluent at 1PET; T4, municipal effluent at 2 PET; and T5, canal water at 1 PET. Observations included plant height, collar diameter at one-month intervals and plant mineral composition, mineral uptake and changes in soil properties at 24 months of plant age. Application of municipal effluent produced better growth in D. sissoo seedlings. Concentrations of nitrogen (N), phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg), copper (Cu), iron (Fe), manganese (Mn) and zinc (Zn) were greater in seedlings irrigated with municipal effluent than those of the seedlings irrigated by the treatment T5, and positively related with the quantity of irrigation. The concentrations were greatest in foliage compared to the other parts of seedling, with the exception of Cu concentration. Application of municipal effluents resulted in a 2- to 3-fold increase in the concentrations of soil K, Cu, Fe, Mn and Zn, whereas NH4-N and PO4-P availability increased by 8.1- and 4.5-fold, respectively. The increase in soil organic carbon was only observed in treatments T3 and T4. The accumulations of soil NO3-N, Na, Cu, Fe, Mn and Zn were more in lower soil layers but the other soil parameters showed their greatest values in the upper soil layer. Irrigation using municipal effluent did not result in toxicity to the seedlings before the age of 24 months. The results suggest that municipal effluent could be utilized, as an important source of water and nutrients in growing D. sissoo to increase biomass production in the needs of suburban dwellers. However, a preliminary treatment to reduce excess NH4-N and PO4-P will be required before application to the plantation.     

Perfusion culture process plus H2O2 stimulation for efficient astaxanthin production by Xanthophyllomyces dendrorhous

A semicontinuous perfusion culture process (repeated medium renewal with cell retention) was evaluated together with batch and repeated fed-batch processes for astaxanthin production in shake-flask cultures of Xanthophyllomyces dendrorhous. The perfusion process with 25% medium renewal every 12 h for 10 days achieved a biomass density of 65.6 g/L, a volumetric astaxanthin yield of 52.5 mg/L, and an astaxanthin productivity of 4.38 mg/L-d, which were 8.4-fold, 5.6-fold, and 2.3-fold of those in the batch process, 7.8 g/L, 9.4 mg/L, and 1.88 mg/L-d, respectively. The incorporation of hydrogen peroxide (H(2)O(2)) stimulation of astaxanthin biosynthesis into the perfusion process further increased the astaxanthin yield to 58.3 mg/L and the productivity to 4.86 mg/L-d. The repeated fed-batch process with 8 g/L glucose and 4 g/L corn steep liquor fed every 12 h achieved 42.2 g/L biomass density, 36.5 mg/L astaxanthin yield, and 3.04 mg/L-d astaxanthin productivity. The lower biomass and astaxanthin productivity in the repeated fed-batch than in the perfusion process may be mostly attributed to the accumulation of inhibitory metabolites such as ethanol and acetic acid in the culture. The study shows that perfusion process plus H(2)O(2) stimulation is an effective strategy for enhanced astaxanthin production in X. dendrorhous cultures.     

Efficient one-step production of astaxanthin by the microalga Haematococcus pluvialis in continuous culture

The performance of Haematococcus pluvialis in continuous photoautotrophic culture has been analyzed, especially from the viewpoint of astaxanthin production. To this end, chemostat cultures of Haematococcus pluvialis were carried out at constant light irradiance, 1,220 microE/m2.s, and dilution rate, 0.9/d, but varying the nitrate concentration in the feed medium reaching the reactor, from 1.7 to 20.7 mM. Both growth and biomass composition were affected by the nitrate supply. With saturating nitrate, the biomass productivity was high, 1.2 g/L.d, but astaxanthin accumulation did not take place, the C/N ratio of the biomass being 5.7. Under moderate nitrate limitation, biomass productivity was decreased, as also did biomass concentration at steady state, whereas accumulation of astaxanthin developed and the C/N ratio of the biomass increased markedly. Astaxanthin accumulation took place in cells growing and dividing actively, and its extent was enhanced in response to the limitation in nitrate availability, with a recorded maximum for astaxanthin cellular level of 0.8% of dry biomass and of 5.6 mg/L.d for astaxanthin productivity. The viability of a significant continued generation of astaxanthin-rich H. pluvialis cells becomes thus demonstrated, as also does the continuous culture option as an alternative to current procedures for the production of astaxanthin using this microalga. The intensive variable controlling the behavior of the system has been identified as the specific nitrate input, and a mathematical model developed that links growth rate with both irradiance and specific nitrate input. Moreover, a second model for astaxanthin accumulation, also as a function of irradiance and specific nitrate input, was derived. The latter model takes into account that accumulation of astaxanthin is only partially linked to growth, being besides inhibited by excess nitrate. Simulations performed fit experimental data and emphasize the contention that astaxanthin can be efficiently produced under continuous mode by adjustment of the specific nitrate input, predicting even higher values for astaxanthin productivity. The developed models represent a powerful tool for management of such an astaxanthin-generating continuous process, and could allow the development of improved systems for the production of astaxanthin-rich Haematococcus cells.     

Efficiency assessment of the one-step production of astaxanthin by the microalga Haematococcus pluvialis

Continuous cultivation of Haematococcus pluvialis under moderate nitrogen limitation represents a straightforward strategy, alternative to the classical two-stage approach, for astaxanthin production by this microalga. Performance of the one-step system has now been validated for more than 40 combinations of dilution rate, nitrate concentration in the feed medium, and incident irradiance, steady state conditions being achieved and maintained in all instances. Specific nitrate input and average irradiance were decisive parameters in determining astaxanthin content of the biomass, as well as productivity of the system. The growth rate of the continuous photoautotrophic cultures was a hyperbolic function of average irradiance. As long as specific nitrate input was above the threshold value of 2.7 mmol/g day, cells performed green and astaxanthin was present at basal levels only. Below the threshold value, under moderate nitrogen limitation conditions, astaxanthin accumulated to reach cellular levels of up to 1.1% of the dry biomass. Increasing irradiance resulted in enhancement of astaxanthin accumulation when nitrogen input was limiting, but never under nitrogen sufficiency. Mean daily productivity values of 20.8 +/- 2.8 mg astaxanthin/L day (1.9 +/- 0.3 g dry biomass/L day) were consistently achieved for a specific nitrate input of about 0.8 mmol/g day and an average irradiance range of 77-110 microE/m(2) s. Models relating growth rate and astaxanthin accumulation with both average irradiance and specific nitrate input fitted accurately experimental data. Simulations provided support to the contention of achieving efficient production of the carotenoid through convenient adjustment of the determining parameters, and yielded productivity estimates for the one-step system higher than 60 mg astaxanthin/L day. The demonstrated capabilities of this production system, as well as its product quality, made it a real alternative to the current two-stage system for the production of astaxanthin-rich biomass.     

一株法夫酵母虾青素高产菌株的生产性能

为了评价虾青素高产菌株-法夫酵母JMU-MVP14的生产性能及建立虾青素高产发酵技术,通过测定糖、生物量、虾青素产量、总类胡萝卜素产量等发酵参数,用摇瓶试验对比了法夫酵母JMU-MVP14和出发菌株的差异,用7 L罐试验对比了pH值调控方式及补料培养基成分对发酵的影响,用1 m3罐试验评估了法夫酵母JMU-MVP14高密度发酵虾青素的产量水平。摇瓶发酵结果表明,法夫酵母JMU-MVP14虾青素及总类胡萝卜素的细胞产率分别达到6.01 mg/g及10.38 mg/g;7 L罐分批发酵试验结果表明,自动流加调     

微量元素对大肠杆菌生长和乙酸生成的影响研究

大肠杆菌DA19的代谢特性与培养基中添加微量元素有较大的关系。在基本培养基中,当氮源限制时,添加微量元素可以在一定程度上改善DA19菌体的生长,提高菌体得率YX/G,大大减少乙酸的生成;当氮源充分时,与不添加微量元素相比,DA19在添加微量元素后,菌体浓度大大增加,虽然葡萄糖消耗速率加快,但产乙酸仍然很少,只有不添加时的13％,YX/G提高至少60％。基本培养基中添加0.1～1mL/L的微量元素混合溶液对DA19菌体生长、乙酸生成及葡萄糖消耗没有显著影响。在单独添加不同种类的微量元素时, BO33-、Zn2+、MoO42+、Cu2+没有特别明显的影响,Al3+会抑制菌体生长和葡萄糖利用,而Co2+、Mn2+、Fe2+可以改善细胞生长,特别是添加Fe2+时,细胞生长及乙酸生成等培养结果与添加微量元素混合溶液几乎相同。