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首页> 外文期刊>Biochemical Engineering Journal >Biodesulfurisation of DBT with Pseudomonas putida CECT5279 by resting cells: Influence of cell growth time on reducing equivalent concentration and HpaC activity
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Biodesulfurisation of DBT with Pseudomonas putida CECT5279 by resting cells: Influence of cell growth time on reducing equivalent concentration and HpaC activity

机译:静息细胞将恶臭假单胞菌CECT5279对DBT进行生物脱硫:细胞生长时间对降低当量浓度和HpaC活性的影响

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Dibenzothiophene(DBT)biodesulfurisation(BDS)route using a genetically modified organism,Pseudomonas putida CECT 5279,is studied.Tests of BDS with whole cells and with homogenized cells are carried out by taking samples of the cells during growth.The influence of the growth phases in the evolution of the intermediates of the 4S DBT desulfurising route is shown.Conversions of the five key compounds of the 4S route(DBT,DBTO,DBTO_2,HBPS and HBP)are measured.DBT conversion values are maximal with cells obtained after 30 h of growth time.HBP conversion values do not coincide with DBT conversion values,the maximum HBP production is obtained with cells grown for 10 h.A greater intermediate DBTO and DBTO_2 accumulation in broth is produced with cells obtained at 5 and 10 h of growth time.Nevertheless,the accumulation in broth of HBPS,another intermediate,is considerably lower than that observed with cells obtained at 23,30 and 45 h of growth time.Also,the concentration of the reducing equivalents(NADH and FMNH_2)and flavin-oxido-reductase activity inside the cells is measured.This showed that the concentration of the reducing equivalents and the activity of the HpaC enzyme in the P.putida cytoplasm do not limit BDS rate.The influence of 4S compound transport across cellular membrane is studied by comparison of results obtained by resting cell assays(whole cells)and with homogenized cells assays(disrupted cells).The results show that there is no accumulation of any compound inside the cells,and that the transport rate across the cellular membrane does not limit the overall biodesulfurisation rate.
机译:研究了使用转基因生物恶臭假单胞菌CECT 5279进行的二苯并噻吩(DBT)生物脱硫(BDS)路线。通过在生长过程中采集细胞样本进行全细胞和均质化细胞的BDS测试。图中显示了4S DBT脱硫途径的中间体的演变阶段。测量了4S途径的五个关键化合物(DBT,DBTO,DBTO_2,HBPS和HBP)的转化率.30分钟后获得的细胞的DBT转化值最大HBP转化率值与DBT转化率值不一致,细胞生长10 h可获得最大HBP产量。在生长5和10 h时获得的细胞可产生更高的中间DBTO和肉汤中DBTO_2积累。然而,另一种中间体HBPS的肉汤中的积累却大大低于在生长时间23、30和45 h所获得的细胞中所观察到的。测定细胞内ts(NADH和FMNH_2)和黄素氧化还原酶的活性,这表明恶臭假单胞菌胞质中还原当量的浓度和HpaC酶的活性均不限制BDS的发生率。通过比较静息细胞试验(整个细胞)和匀浆细胞试验(破裂的细胞)获得的结果,研究了4S化合物跨细胞膜的转运。结果表明,细胞内没有任何化合物的积累,并且转运跨细胞膜的速率不限制整体生物脱硫速率。

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