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透明颤菌血红蛋白基因在银耳中的染色体整合及其生理作用。

Chromosomal integration of the Vitreoscilla hemoglobin gene and its physiological actions in Tremella fuciformis.

作者信息

Zhu Hu, Wang Tian-Wen, Sun Shu-Jing, Shen Ya-Ling, Wei Dong-Zhi

机构信息

State Key Laboratory of Bioreactor Engineering, New World Institute of Biotechnology, East China University of Science and Technology, Shanghai 200237, People's Republic of China.

出版信息

Appl Microbiol Biotechnol. 2006 Oct;72(4):770-6. doi: 10.1007/s00253-006-0322-9. Epub 2006 Feb 25.

Abstract

The Vitreoscilla hemoglobin (VHb) gene was expressed in yeast-like conidia (YLCs) of Tremella fuciformis (T. fuciformis) to increase cell density in submerged fermentation by enhancing oxygen uptake. With the intention of doing this, an integrated expression vector containing the VHb gene and the hygromycin B phosphotransferase (hph) gene derived from Escherichia coli (E. coli) as the selectable marker was constructed, and then transformed into protoplasts of YLCs from T. fuciformis with restriction enzyme-mediated DNA integration (REMI). Hygromycin-resistant transformants had been generated during the transformation. Molecular evidences including PCR assay, Southern blotting, and Western blot analysis indicated the VHb gene had been integrated into the genome of transgenic T. fuciformis strains and was expressed successfully. Shake-flask fermentation and bioreactor cultivation results showed that the expression of VHb in this fungus could enhance growth of YLCs. The final cell density was higher in the culture of VHb-expressing strain than that of the wild-type strain. Moreover, these results also suggested that CaMV35S promoter was capable of driving the expression of heterologous genes in T. fuciformis.

摘要

将透明颤菌血红蛋白(VHb)基因在银耳的酵母状分生孢子(YLCs)中表达,以通过增强氧气摄取来提高深层发酵中的细胞密度。为此,构建了一个包含VHb基因和源自大肠杆菌(E. coli)的潮霉素B磷酸转移酶(hph)基因作为选择标记的整合表达载体,然后通过限制酶介导的DNA整合(REMI)将其转化到银耳YLCs的原生质体中。转化过程中产生了潮霉素抗性转化体。包括PCR检测、Southern杂交和Western印迹分析在内的分子证据表明,VHb基因已整合到转基因银耳菌株的基因组中并成功表达。摇瓶发酵和生物反应器培养结果表明,该真菌中VHb的表达可促进YLCs的生长。表达VHb的菌株培养物中的最终细胞密度高于野生型菌株。此外,这些结果还表明CaMV35S启动子能够驱动异源基因在银耳中的表达。

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