scholarly journals Biodiesel synthesis by a one-step method in a genetically engineered Escherichia coli using rice straw hydrolysate and restaurant oil wastes as raw materials

2012 ◽  
Vol 113 (3) ◽  
pp. 531-540 ◽  
Author(s):  
B. Wang ◽  
H. Lin ◽  
J. Zhan ◽  
Y. Yang ◽  
Q. Zhou ◽  
...  
2020 ◽  
Vol 14 (2) ◽  
pp. 121-133 ◽  
Author(s):  
Maryam Ahankoub ◽  
Gashtasb Mardani ◽  
Payam Ghasemi-Dehkordi ◽  
Ameneh Mehri-Ghahfarrokhi ◽  
Abbas Doosti ◽  
...  

Background: Genetically engineered microorganisms (GEMs) can be used for bioremediation of the biological pollutants into nonhazardous or less-hazardous substances, at lower cost. Polycyclic aromatic hydrocarbons (PAHs) are one of these contaminants that associated with a risk of human cancer development. Genetically engineered E. coli that encoded catechol 2,3- dioxygenase (C230) was created and investigated its ability to biodecomposition of phenanthrene and pyrene in spiked soil using high-performance liquid chromatography (HPLC) measurement. We revised patents documents relating to the use of GEMs for bioremediation. This approach have already been done in others studies although using other genes codifying for same catechol degradation approach. Objective: In this study, we investigated biodecomposition of phenanthrene and pyrene by a genetically engineered Escherichia coli. Methods: Briefly, following the cloning of C230 gene (nahH) into pUC18 vector and transformation into E. coli Top10F, the complementary tests, including catalase, oxidase and PCR were used as on isolated bacteria from spiked soil. Results: The results of HPLC measurement showed that in spiked soil containing engineered E. coli, biodegradation of phenanthrene and pyrene comparing to autoclaved soil that inoculated by wild type of E. coli and normal soil group with natural microbial flora, were statistically significant (p<0.05). Moreover, catalase test was positive while the oxidase tests were negative. Conclusion: These findings indicated that genetically manipulated E. coli can provide an effective clean-up process on PAH compounds and it is useful for bioremediation of environmental pollution with petrochemical products.


2013 ◽  
Vol 35 (5) ◽  
pp. 689-693 ◽  
Author(s):  
Baosheng Ge ◽  
Yan Li ◽  
Haixiang Sun ◽  
Shuai Zhang ◽  
Peijie Hu ◽  
...  

2012 ◽  
Vol 476-478 ◽  
pp. 194-198 ◽  
Author(s):  
Zhi Chao Chen ◽  
Zheng Liang Xue ◽  
Wei Wang ◽  
Yue Yu ◽  
Qiang Liu ◽  
...  

Keywords: vanadium pentoxide;carbon black;reduction and nitridation;vanadium nitrogen alloy. Abstract. The V2O5 extracted from low vanadium shale and carbon black are used as raw materials to prepare briquetting samples through mixing, grinding and pressing. The samples are prereduced, final reduced and nitrated to produce vanadium nitrogen alloy with high nitrogen content. Thermodynamic analysis and experiment results show that:(1)In order to avoid V2O5 volatilization loss during reduction, the briquetting samples should be pre-reduced for 4 hours below the melting point 670°C of V2O5, which can transform V2O5 into low valence vanadium oxide.(2)During V2O5 being self-reduction under N2 atmosphere, if the final reduction temperature is below 1271°C, the VN is preferential formation; if more than 1271°C, the reduced product forms V4C3.(3)To make a product with high nitrogen and low carbon content, the final reduction and nitride temperature should be controlled below 1300°C.


2019 ◽  
Vol 366 (24) ◽  
Author(s):  
Yan Ge ◽  
Senlin Guo ◽  
Tao Liu ◽  
Chen Zhao ◽  
Duanhua Li ◽  
...  

ABSTRACT A nuclease from Yersinia enterocolitica subsp. palearctica (Nucyep) is a newly found thermostable nonspecific nuclease. The heat-resisting ability of this nuclease would be extremely useful in biological research or pharmaceutical production. However, the application of this nuclease is limited because of its poor yield. This research aimed to improve Nucyep productivity by producing a novel genetically engineered Escherichia coli and optimizing the production procedures. After 4 h of induction by lactose, the new genetically engineered E. coli can express a substantial amount of Nucyep in the form of inclusion bodies. The yield was approximately 0.3 g of inclusion bodies in 1 g of bacterial pellets. The inclusion bodies were extracted by sonication and solubilized in an 8 M urea buffer. Protein renaturation was successfully achieved by dilution method. Pure enzyme was obtained after subjecting the protein solution to anion exchange. The Nucyep showed its nonspecific and heat resistant properties as previously reported (Boissinot et  al. 2016). Through a quantification method, its activity was determined to be 1.3 × 10 6 Kunitz units (K.U.)/mg. These results can serve as a reference for increasing Nucyep production.


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