首页> 外文期刊>Applied Biochemistry and Biotechnology >A Process to Produce Penicillin G Acylase by Surface-Adhesion Fermentation Using Mucor griseocyanus to Obtain 6-Aminopenicillanic Acid by Penicillin G Hydrolysis
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A Process to Produce Penicillin G Acylase by Surface-Adhesion Fermentation Using Mucor griseocyanus to Obtain 6-Aminopenicillanic Acid by Penicillin G Hydrolysis

机译:一种利用Mucor griseocyanus通过表面黏附发酵生产青霉素G酰基转移酶的方法,该方法通过青霉素G的水解获得6-氨基戊酸

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The production of extracellular and mycelia-associated penicillin G acylase (maPGA) with Mucor griseocyanus H/55.1.1 by surface-adhesion fermentation using Opuntia imbricata, a cactus, as a natural immobilization support was studied. Enzyme activity to form 6-aminopencillanic acid (6-APA) from penicillin G was assayed spectrophotometrically. The penicillin G hydrolysis to 6-APA was evaluated at six different times using PGA samples recovered from the skim milk medium at five different incubation times. Additionally, the effect of varying the penicillin G substrate concentration level on the PGA enzyme activity was also studied. The maximum reaction rate, V max, and the Michaelis constant, K M, were determined using the Michaelis–Menten model. The maximum levels for maPGA and extracellular activity were found to be 2,126.50 international unit per liter (IU/l; equal to 997.83 IU/g of support) at 48 h and 755.33 IU/l at 60 h, respectively. Kinetics of biomass production for total biomass showed a maximum growth at 60 h of 3.36 and 2.55 g/l (equal to 0.012 g of biomass per gram of support) for the immobilized M. griseocyanus biomass. The maPGA was employed for the hydrolysis of penicillin G to obtain 6-APA in a batch reactor. The highest quantity of 6-APA obtained was 226.16 mg/l after 40-min reaction. The effect of substrate concentration on maPGA activity was evaluated at different concentrations of penicillin G (0–10 mM). K M and V max were determined to be 3.0 × 10−3 M and 4.4 × 10−3 mM/min, respectively.
机译:研究了使用仙人掌仙人掌(仙人掌)作为天然固定载体,通过表面黏附发酵生产带有Mucor griseocyanus H / 55.1.1的细胞外和与菌丝体相关的青霉素G酰基转移酶(maPGA)。分光光度法测定了从青霉素G生成6-氨基青霉酸(6-APA)的酶活性。使用从脱脂牛奶培养基中回收的PGA样品在五个不同的孵育时间,在六个不同的时间评估了青霉素G水解成6-APA的能力。另外,还研究了改变青霉素G底物浓度水平对PGA酶活性的影响。使用Michaelis–Menten模型确定最大反应速率V max 和米氏常数K M 。发现在48小时时maPGA和细胞外活性的最高水平分别为每升2,126.50国际单位(IU / l;等于997.83 IU / g支持物),在60 h时为755.33 IU / l。总生物量的生物量生产动力学显示,固定化灰黄藻生物量在60 h时最大增长为3.36和2.55 g / l(相当于每克载体0.012 g生物量)。将maPGA用于青霉素G的水解,以在间歇反应器中获得6-APA。反应40分钟后获得的最高6-APA量为226.16 mg / l。在不同浓度的青霉素G(0–10 mM)下评估了底物浓度对maPGA活性的影响。确定K M 和V max 为3.0×10 -3 M和4.4×10 -3 mM / min。

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