首页> 外文期刊>BMC Biotechnology >High level production of tyrosinase in recombinant Escherichia coli
【24h】

High level production of tyrosinase in recombinant Escherichia coli

机译:重组大肠杆菌中酪氨酸酶的大量生产

获取原文
获取外文期刊封面目录资料

摘要

Background Tyrosinase is a bifunctional enzyme that catalyzes both the hydroxylation of monophenols to o -diphenols (monophenolase activity) and the subsequent oxidation of the diphenols to o -quinones (diphenolase activity). Due to the potential applications of tyrosinase in biotechnology, in particular in biocatalysis and for biosensors, it is desirable to develop a suitable low-cost process for efficient production of this enzyme. So far, the best production yield reported for tyrosinase was about 1?g?L-1, which was achieved by cultivating the filamentous fungus Trichoderma reesei for 6?days . Results In this work, tyrosinase from Verrucomicrobium spinosum was expressed in Escherichia coli and its production was studied in both batch and fed-batch cultivations. Effects of various key cultivation parameters on tyrosinase production were first examined in batch cultures to identify optimal conditions. It was found that a culture temperature of 32?°C and induction at the late growth stage were favorable, leading to a highest tyrosinase activity of 0.76 U mL-1. The fed-batch process was performed by using an exponential feeding strategy to achieve high cell density. With the fed-batch process, a final biomass concentration of 37?g?L-1 (based on optical density) and a tyrosinase activity of 13 U mL-1 were obtained in 28?hours, leading to a yield of active tyrosinase of about 3?g?L-1. The highest overall volumetric productivity of 103?mg of active tyrosinase per liter and hour (corresponding to 464?mU?L-1?h-1) was determined, which is approximately 15 times higher than that obtained in batch cultures. Conclusions We have successfully expressed and produced gram quantities per liter of active tyrosinase in recombinant E. coli by optimizing the expression conditions and fed-batch cultivation strategy. Exponential feed of substrate helped to prolong the exponential phase of growth, to reduce the fermentation time and thus the cost. A specific tyrosinase production rate of 103?mg?L?1?h?1 and a maximum volumetric activity of 464?mU?L?1?h-1 were achieved in this study. These levels have not been reported previously.
机译:背景技术酪氨酸酶是一种双功能酶,其催化单酚的羟基化为邻二酚(单酚酶活性)和随后的二酚氧化为邻醌(二酚酶活性)。由于酪氨酸酶在生物技术中,特别是在生物催化中和在生物传感器中的潜在应用,期望开发一种合适的低成本方法以有效生产这种酶。迄今为止,据报道,酪氨酸酶的最佳产量约为1?g?L -1 ,这是通过将丝状真菌里氏木霉培养6天来实现的。结果在这项工作中,来自棘皮疣状疣的酪氨酸酶在大肠杆菌中表达,并在分批和分批分批培养中研究了其产生。首先在分批培养中检查了各种关键培养参数对酪氨酸酶生产的影响,以确定最佳条件。结果表明,培养温度为32℃,生长后期诱导较为有利,酪氨酸酶活性最高,为0.76 U mL -1 。补料分批工艺是通过使用指数补料策略来实现的,以实现高细胞密度。通过分批补料工艺,最终生物量浓度为37?g?L -1 (基于光密度),酪氨酸酶活性为13 U mL -1 在28小时内即可获得,因此活性酪氨酸酶的产量约为3?g?L -1 。确定了最高的总容积生产率,每升和每小时103?mg活性酪氨酸酶(相当于464?mU?L -1 ?h -1 ),即大约比分批培养获得的高15倍。结论通过优化表达条件和分批补料培养策略,我们已经成功地在重组大肠杆菌中表达并产生了每升活性酪氨酸酶克数。底物的指数进料有助于延长生长的指数期,减少发酵时间并因此降低成本。酪氨酸酶的比生产率为103?mg?L ?1 ?h ?1 ,最大体积活度为464?mU?L ?1 ?h -1 在本研究中获得了。这些水平以前没有报告过。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号