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利用琼脂糖凝胶中长春花固定化原生质体生产细胞壁积累酶。

Production of cell wall accumulative enzymes using immobilized protoplasts of Catharanthus roseus in agarose gel.

作者信息

Mera Nobuaki, Aoyagi Hideki, DiCosmo Frank, Tanaka Hideo

机构信息

Institute of Applied Biochemistry, University of Tsukuba, Tsukuba, Ibaraki 305-8572, Japan.

出版信息

Biotechnol Lett. 2003 Oct;25(20):1687-93. doi: 10.1023/a:1026025617123.

Abstract

Catharanthus roseus cells and protoplasts were used for production of peroxidase and alpha-galactosidase which are accumulated in the cell wall. Only 4% (0.026 U ml(-1)) of the total peroxidase was secreted into the broth by cultured cells while in cultured protoplasts, 45% (0.12 U ml(-1)) was secreted. Protoplasts were protected against the physical and osmotic stresses by immobilizing them in 3% agarose gel (high mass transfer, non-electric charge, low gelation temperature). In order to increase peroxidase production, the immobilized protoplasts were cultivated in shake cultures at low osmotic pressure (12.3 to 16.4 atm) without disruption. During batch peroxidase production, the total activities obtained with free cells at 4.9 atm, free protoplasts at 19.3 atm, and immobilized protoplasts at 12.3 atm were 0.17, 2.54, and 5.16 U, respectively. When four repeated-batch cultures of the immobilized protoplasts were performed at 16.4 atm, 11.8 U of peroxidase was obtained. This system was also useful for the production of alpha-galactosidase.

摘要

长春花细胞和原生质体被用于生产过氧化物酶和α-半乳糖苷酶,这些酶积累在细胞壁中。培养细胞仅将总过氧化物酶的4%(0.026 U ml⁻¹)分泌到培养液中,而在培养的原生质体中,45%(0.12 U ml⁻¹)被分泌出来。通过将原生质体固定在3%琼脂糖凝胶中(传质率高、无电荷、凝胶化温度低)来保护它们免受物理和渗透胁迫。为了提高过氧化物酶的产量,将固定化原生质体在低渗透压(12.3至16.4个大气压)下进行摇瓶培养而不被破坏。在分批生产过氧化物酶的过程中,在4.9个大气压下的游离细胞、19.3个大气压下的游离原生质体和12.3个大气压下的固定化原生质体所获得的总活性分别为0.17、2.54和5.16 U。当在16.4个大气压下对固定化原生质体进行四次重复分批培养时,获得了11.8 U的过氧化物酶。该系统也可用于生产α-半乳糖苷酶。

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