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1.
Bacillus mesentericus was found to assimilate nucleic acids as a source of nitrogen and phosphorus. Nucleic acids added to the medium as a source of nitrogen or phosphorus stimulated synthesis of ribonuclease. When washed bacterial cells were incubated for a short period of time in a fresh nutrient medium containing RNA, synthesis of RNAase was also induced. Synthesis of the enzyme was inhibited by high concentrations of chloramphenicol and actinomycin D, and stimulated by low concentrations of actinomycin D. Therefore, alkaline RNAase is an inducible enzyme which participates in the nutrition processes of bacteria.  相似文献   

2.
The effect of phosphorus on biosynthesis of polymyxin B by B. polymyxa 1538 was studied and its optimal concentration in the synthetic and two complex media was determined. Correlation between the culture growth and consumption of the main components, on the one hand, and concentration of phosphorus in the medium, on the other hand, was found. It was shown that the effect of phosphorus on biosynthesis of polymyxin B did not depend on the carbon source in the medium and aeration conditions.  相似文献   

3.
I V Gracheva  N V Orlova 《Antibiotiki》1975,20(10):871-876
According to the literature data biosynthesis of novobiocin by Act. spheroides unlike other antibiotics does not practically depend on the phosphorus levels in the medium. In the present paper it is shown that production of novobiocin in natural media is sensitive to the concentration of mineral phosphorus in the medium. The optimal concentration of phosphorus for biosynthesis of novobiocin is almost within the same ranges as that for biosynthesis of streptomycin, tetracyclines and oleandomycin.  相似文献   

4.
A synthetic medium containing optimal levels of the sources of carbon, nitrogen and inorganic phosphorus and providing satisfactory yields of polymyxin B was developed for 2 strains of Bac. polymyxa 933 and VK-153. The consumption of phosphorus in the medium by the strains and the antibiotic biosynthesis levels depended on the form of phosphorus added to the medium. Optimal biosynthesis of polymyxin B was observed at lower concentration levels of soluble soluble phosphorus in the medium than the bacterial growth.  相似文献   

5.
在常氧孵育中,当孵育介质自由钙离子浓度升高时,离体心肌线粒体钙含量显著增加。同时,线粒体状态4呼吸速率也明显加快并与其钙含量的增加呈正相关关系。在低氧孵育中,当孵育介质自由钙离子浓度升高时,离体心肌线粒体钙含量没有明显的增加,其状态4呼吸速率虽有加快但程度明显较常氧孵育时低。另外,在低孵育介质自由钙离子浓度(pCa8.0)的条件下,低氧可引起轻微的线粒体状态4呼吸速率加快。从以上结果作者推测,低氧引起心肌细胞的线粒体损伤可能主要不是低氧直接对线粒体作用所造成的,而是由低氧引起的心肌细胞胞浆环境变化对线粒体破坏的结果。其中胞浆自由钙离子的升高可能是一个的原因。  相似文献   

6.
Studying relationships between tobacco mosaic virus reproduction, anthocyanin biosynthesis and phosphorus content in cultivation medium, it was found thatMartin's (1958) finding of an indirect proportion between anthocyanin and virus synthesis is valid even under the complicated conditions of pathological anthocyanin formation induced by phosphorus deficiency. A decrease of anthocyanin biosynthesis with simultaneous stimulation of virus reproduction takes place at temperatures below 20°C. Increased anthocyanin biosynthesis accompanied with the inhibition of virus reproduction occurs at temperatures above 20°C. The obtained results suggest that enzyme systems and substrates participating in considerably increased anthocyanin biosynthesis induced by phosphorus deficiency, differ from those taking part in anthocyanin synthesis induced by virus infection. The enhanced phosphorus content in the cultivation medium does not influence anthocyanin biosynthesis significantly. Nevertheless, a highly significant inhibition of tobacco mosaic virus reproduction takes place at temperatures above 20°C. This inhibition may be in correlation with some other metabolic systems affected probably by the enhanced phosphorus concentration in the nutrient medium.  相似文献   

7.
The optimal concentrations of mineral phosphorus for the growth of the tobramycin-producing organism and for the production of the antibiotic by it in the synthetic medium were determined. Introduction of an additional source of mineral phosphorus into the rich soybean medium resulted in decreased levels of antibiotic production. The stimulating effect of manganese sulfate on the biosynthesis of tobramycin in the rich medium was shown. The stimulating effect of soybean, linseed and palm oils on the production of tobramycin was evident when the fermentation period was longer.  相似文献   

8.
Attempts were devoted to use Streptomyces aureofaciens and Streptomyces erythreus, the antibiotics producers as sources for the biosynthesis of cobalamine. The constituents of the fermentation medium and the strain play an important role in the biosynthesis of vitamin B12. The same strain produced different amounts of antibiotic and vitamin on the two different constitutive media. The increase of the phosphorus concentration in the fermentation medium—within limits—increased the vitamin B12 biosynthesis. The optimal concentration of phosphorus favourable for the synthesis of cobalamine was inhibitive for the antibiotic production. The phosphorus level in the fermentation medium plays an important role in the metabolism of carbohydrate and consequently on the biosynthesis of antibiotics. Low concentration of 5,6-dimethylbenzimidazole (cobalamine precursor) in the presence of suitable phosphorus induced the microorganism to increase its biosynthetic potentiality for the vitamin B12 production.  相似文献   

9.
When glucose is substituted for sucrose in the fermentation medium for Streptomyces antibioticus, the pH of the cultural broth becomes more acidic, the rate of protein synthesis in the mycelium rises, and the rate of oleandomycin synthesis decreases abruptly. The dynamics of cAMP (cyclic monophosphate) accumulation was studied in the process of biosynthesis by the culture in different media. Most of the synthesized cAMP (80-90%) was shown to be excreted into the medium. Glucose stimulates cAMP synthesis and excretion from the mycelium by a factor of 1.5-3. No distinct correlation was found between cAMP content in S. antibioticus cells and the level of oleandomycin biosynthesis. A correlation between changes in the concentration of exocellular cAMP and protein synthesis in the mycelium suggests that the excreted cAMP may be involved in regulating the growth of the culture producing the antibiotic.  相似文献   

10.
Cytotoxicity of RNAase from Bacillus intermedius was studied in vitro and in vivo. It was shown that the enzyme had slightly pronounced cytotoxicity according to the tests with inhibition of cell proliferation and biosynthesis of cell nucleic acids. The RNAase was also shown to impair the vital staining by neutral red. The efficiency of the impairment much more depended on the enzyme catalytic activity than on the proliferation and biosynthesis of nucleic acids. In vivo toxicity of RNAase from B. intermedius was 3-5 times higher than that of pancreatic RNAase. Possible mechanisms of the different toxicity of the enzymes are discussed.  相似文献   

11.
The effect of RNAase A on the activation of the estrogen receptor from fetal guinea pig uterus was studied by DNA-cellulose binding assay and immunorecognition of the estradiol-receptor complex by the monoclonal antibody D547 raised against the human estrogen receptor. After RNAase treatment at 4 degrees C or 25 degrees C the binding of the receptor to DNA-cellulose doubled. This stimulation was partially prevented by sodium molybdate. RNAase treatment did not modify the interaction of the receptor with the monoclonal antibody D547; this antibody, as was demonstrated previously, selectively recognizes the activated form of the receptor when activation has been induced by temperature, time or high salt concentrations. In addition, RNAase had little or no effect on the transformation of the 8-9 S receptor to more slowly sedimenting forms under low salt concentrations. These observations suggest that even if RNAase induces receptor activation, which can be inferred from the increase in its binding to DNA-cellulose, the conformational modifications of the receptor molecule involved in this process are apparently different from those induced by factors such as temperature, time or high-salt concentrations.  相似文献   

12.
研究了磷酸盐限量对产甘油假丝酵母甘油合成与胞内磷积累的影响。结果表明, 当酵母细胞从适磷或富磷培养基转接入低磷培养基时, 发酵过程中胞内积累的磷逐渐减少; 而当菌体从低磷培养基转接入适磷或富磷培养基时, 发酵过程中胞内聚磷酸盐的积累量迅速增加。当细胞在第14小时和第38小时从适磷培养基转接入低磷培养基时甘油得率分别高达60.9%和61.4%, 而甘油产率则分别为2.03 g/(L·h)和2.23 g/(L·h)。这些现象说明限制发酵培养基中的磷浓度是产甘油假丝酵母高产甘油的必要条件, 并为其反复分批发酵法生产甘油提供了重要依据。  相似文献   

13.
氮磷浓度对藻-溞-草间相互作用的影响   总被引:2,自引:0,他引:2  
为了解氮磷浓度对生物操纵效果的影响, 以小球藻、大型溞和金鱼藻分别作为浮游植物、浮游动物和大型沉水植物的代表, 建立了它们之间相互作用的水生微宇宙模型。研究了在25℃、2000—3000 lx 的温度和光照下, 不同氮磷浓度对三者生长的影响。结果表明: 两者共培养时, 在高氮(10.5 mg/L)条件下, 磷浓度小于0.1 mg/L 对大型溞繁殖和金鱼藻的生长有利; 磷浓度介于0.1—2 mg/L 时小球藻呈大暴发趋势, 而金鱼藻的生长则明显受抑制。在低氮(0.5 mg/L)条件下, 磷浓度不大于0.5 mg/L, 大型溞对小球藻有较好的抑制作用, 金鱼藻与小球藻无显著互抑现象; 磷浓度增大为2 mg/L 时, 小球藻对金鱼藻生长产生明显抑制。在0.05—2 mg/L 的磷浓度范围及高氮和低氮条件下三者共培养时, 大型溞数量及金鱼藻生物量均不同程度的升高,且小球藻数量得到了有效抑制, 以磷浓度为0.1—0.5 mg/L 时效果最佳; N/P 比值对藻、溞、草间的相互作用有重要影响, 在藻-溞系统中, 大型沉水植物的加入可以大大提高控藻效果, 减小N/P 比值波动带来的不利影响。与低氮情况相比, 高氮条件对金鱼藻、大型溞及小球藻的增长均存在一定抑制作用。磷浓度为0.5 mg/L时的水体氮磷去除效果好于其他磷浓度梯度。    相似文献   

14.
Glycerol as the sole carbon source was added to the medium or biosynthesis of heliomycin by Streptomyces olivocinereus and the effect of its concentration on the culture growth and antibiotic production was studied. The culture growth and the amount of the antibiotic synthesized per 1 unit of the fermentation broth were limited by glycerol added in quantities of 0.05 to 1 per cent. Further increasing of the glycerol concentration had no significant effect on the culture growth and antibiotic biosynthesis. The amount of the antibiotic synthesized per 1 unit of the mycelial mass relatively slightly depended on the glycerol concentration. The rate of glycerol consumption by the young 24-hour culture in batch fermentations markedly exceeded that of glycerol consumption by the 48-hour culture. The younger mycelium significantly increased its rate of glycerol consumption when the initial concentration was increased whereas the rate of glycerol consumption by the more mature mycelium did not depend on the initial concentration of the carbon source (within 0.5-2 per cent). The rate of heliomycin biosynthesis practically slightly depended on the initial concentration of glycerol.  相似文献   

15.
为了解磷浓度对水生植被恢复和生物操纵效果的影响, 分别用小环藻(Cyclotella sp.)、大型溞(Daphnia magna)和金鱼藻(Ceratophyllum demersum)代表浮游植物、浮游动物和大型沉水植物建立水生微宇宙模型, 在25℃、2600 lx光强和11 mg/L氮浓度条件下, 分别研究小环藻与大型溞、小环藻与金鱼藻、小环藻-大型溞-金鱼藻共培养时4种磷浓度(0.05、0.1、0.5和2 mg/L)下小环藻、大型溞、金鱼藻的增长率以及培养液中氮磷去除率的变化。结果表明: 小环藻与大型溞、小环藻与金鱼藻两两共培养时, 磷浓度为0.05-2 mg/L时, 金鱼藻和大型溞均生长良好, 小环藻受到明显抑制, 其密度保持较小幅度的正增长。在小环藻-大型溞-金鱼藻三者共培养时, 在0.05-2 mg/L的磷浓度范围内大型溞和金鱼藻生长良好, 与两两共培养相比, 小环藻则受到了更大程度的抑制, 在磷浓度为0.05-0.1 mg/L时藻密度呈现负增长. 这说明在水生态系统中, 大型浮游动物和沉水植物对浮游藻类的联合控制效果远好于各自单独的控制效果, 该控制效果随磷浓度的提高而减弱, 以0.1 mg/L的磷浓度为最佳。在实验结束后测定氮磷去除率发现, 在最低磷浓度(0.05 mg/L),即磷限制时, 水中磷去除率最高, 在最高磷浓度(2 mg/L), 即氮限制时, 水中氮去除率最高。  相似文献   

16.
采用沙培试验对水曲柳幼苗磷胁迫与叶绿素合成、光合作用和生物量分配的关系进行了研究.结果表明,在磷胁迫下,水曲柳幼苗叶片内5-氨基乙酰丙酸(ALA)合成速率和胆色素原(PBG)合成酶活性下降,但叶片中叶绿素a、叶绿素b、总叶绿素以及类胡萝卜素含量没有显著变化;水曲柳幼苗叶片和根中N浓度下降。P在各个部位的浓度也相应减少。表明N和P在苗木生理过程中具有协同作用.叶片中N浓度下降引起光系统Ⅱ(PSⅡ)最大光量子效率(Fv/Fm)、PSⅡ的光化学效率(ΦpsⅡ)、电子传递速率(ETR)以及最大光合速率(Amax)下降.磷胁迫对叶绿素合成的影响与Amax下降无关.在磷胁迫下,水曲柳幼苗总生物量下降,且生物量分配倾向于地下部分。而在P充足或过剩条件下,生物量主要分配于地上部分.  相似文献   

17.
为了解氮浓度对生物操纵和草-藻竞争的影响, 选取铜绿微囊藻、大型溞和金鱼藻分别作为浮游植物、浮游动物和沉水植物的代表, 在温度25℃, 光强2600 lx, 光暗比14h﹕10h, 磷浓度1.5 mg/L时, 研究5种氮浓度(0.5、2、4、8和16 mg/L, 用KNO3溶液配制)下, 溞-藻, 草-藻和溞-草-藻共培养时各自的增长率和培养液中氮磷削减率的变化。结果表明: 在单独培养铜绿微囊藻时, 氮浓度控制在1.97 mg/L以下, 可有效降低培养液中藻的增长率。在溞-藻共培养时, 大型溞有效控藻的氮浓度范围为0.5—4 mg/L; 在草-藻共培养时, 有效控藻的氮浓度范围为0.5—2 mg/L, 对应氮浓度下(0.5和2 mg/L), 实验末期铜绿微囊藻细胞密度分别是溞-藻共培养的23.89%和21.51%, 控藻效果更好; 在溞-草-藻三者共培养时, 有效控藻的氮浓度范围为0.5—16 mg/L, 且氮浓度为0.5—4 mg/L时, 大型溞和金鱼藻的增长率均显著大于铜绿微囊藻, 铜绿微囊藻的增长率均为负值, 控藻效果最好。大型沉水植物的加入, 可以有效提高生物操纵的控藻效果, 减少水中氮磷含量, 长期有效地改善水质。  相似文献   

18.
We have developed a rapid and sensitive method for detecting ribonuclease (RNAase). The method makes use of a RNa-Pyronine Y complex which has a different absorption spectrium from that of Pyronine Y alone. When the RNA is hydrolyzed by RNAase, the spectrum of the complex changes to that of unbound Pyronine Y. The resultant decrease in absorbance at 572 nm is linear for final RNAase concentrations ranging from 2 to 45 ng/ml. Optimal assay conditions were 11.5 μg/ml Pyronine Y, 0.56 mg/ml RNA, 80 μmol/ml Tris-HCl buffer, pH 7.8 and 2–45 ng/ml RNAase. The effect of complex concentration, PH, molarity and temperature upon the rate of the reaction were determined.The assay is applicable to crude cell-free extracts.  相似文献   

19.
The effect of a carbohydrate component of the medium, trace elements and aeration on biosynthesis of the alkaloids costaclavine and epicostaclavine was studied with Penicillium gorlenkoanum. Alkaloid biosynthesis was shown to depend on the nature of a carbohydrate component: virtually no alkaloids were accumulated in media with glucose and fructose although these were synthesized at a high rate in a medium with mannitol. The quantity of synthesized alkaloids and the dynamics of the biosynthesis depended on carbohydrate concentration. The growth and alkaloid synthesis were influenced by traces of zinc, iron, copper and manganese. A more intensive aeration stimulated biomass accumulation but suppressed alkaloid biosynthesis.  相似文献   

20.
Escherichia coli strains BN and CAN are unable to support the growth of bacteriophage T4 psu1+-amber double mutants. For strain BN, this phenotype has been attributed to a defect in 3′ processing of the precursor to psu1+ tRNASer. Since RNAase D and RNAase II are the only well-characterized 3′ exoribonucleases to be implicated in tRNA processing, the status of these activities and their genes in the mutant strains was investigated. Although extracts of strains BN and CAN were defective for hydrolysis of the artificial tRNA precursor, tRNA-C-U, these strains contained normal levels of RNAase D and RNAase II, and purified RNAase D or RNAase II could only partially complement the mutant extracts. Introduction of the wild-type RNAase D gene into strains BN and CAN did not correct the mutant phenotype. Likewise, strains defective in RNAase D and/or RNAase II plated T4psu1+-amber phage normally. These results indicate that the tRNA processing defect in strains BN and CAN is not due to a mutation in either RNAase U or RNAase II. The possibility that the mutation in these strains affects another exoribonuclease or a factor influencing the activity and specificity of RNAase D or RNAase II is discussed.  相似文献   

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