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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2009, Vol. 29 Issue (04): 56-60    
研究报告     
福氏痢疾杆菌组氨酸合成中双功能焦磷酸水解酶和磷酸核糖环化水解酶双功能蛋白的初步研究
陆庆宇1,王其海2,张占钰1,袁道鹏1,高伟1,仓怀兴2,毕汝昌2
1. 北京林业大学理学院
2. 中国科学院生物物理所
cyclohydrolase/Phosphoribosyl-ATP pyrophosphatase In Histidine Biosynthesis Pathway From Shigella flexneri 2a
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摘要: 福志贺氏菌属是一类革兰氏阴性杆菌,是引起人类细菌性痢疾的主要致病源。以福志贺氏痢疾杆菌2a型301株全基因组为模板、以pET22b-(+)为载体、克隆了一个关键基因:组氨酸合成途径中双功能焦磷酸水解酶和磷酸核糖环化水解酶蛋白(简称:sf2088)。以BL21(DE3)为表达菌株,优化表达条件,获得了可溶表达的蛋白。经过亲和层析和分子筛层析获得目标蛋白。采用分析超速离心和动态光散射实验,对纯化后的蛋白进行稳定聚集状态的条件搜索,结果发现锌离子对稳定其聚合状态很重要。通过正交实验,获得蛋白保持稳定聚集态的条件。这对该酶的进一步研究奠定了基础。
关键词: 组氨酸合成途径;双功能蛋白;PR-ATP焦磷酸水解酶和PR-AMP解环酶;表达与纯化    
Abstract: The metabolic pathway of histidine biosynthesis is significant for its various gene organizations and protein structures. HisI/E gene, that can express a bifunctional phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-pyrophosphatase protein, which could catalyze the second and the third step in the histidine biosynthetic pathway, has been successfully cloned by using Shigella flexneri 2α(strain 301) genomic DNA as PCR temple. The protein was soluble expressed in pET22b vector, and purified by Ni-NTA cartridge and Superdex75 molecular filter. Then the soluble highly purified protein was characterized by preliminary crystal analysis, including dynamic light scattering, Analytical Ultracentrifugation and initially screened with Crystal Screens I and II and Index Screen (Hampton Research). The buffer of 50mmol/L Tris–HCl, pH 10.0, 300mmol/L NaCl, 0.05mmol/L ZnCl2 is the best solution for both the maintenance of oligomerization state of the protein and crystallization.
Key words: histidine biosynthesis pathway;bifunctional protein;phosphoribosyl-AMP cyclohydrolase/phosphoribosyl-ATP pyrophosphatase;expressing and purification
收稿日期: 2008-11-06 出版日期: 2009-04-27
基金资助:

国家林业局重点项目(编号:2006-59),中国科学院创新项目;中国科学院创新项目

通讯作者: 高伟   
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陆庆宇
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张占钰
袁道鹏
高伟
仓怀兴
毕汝昌

引用本文:

陆庆宇,王其海,张占钰,袁道鹏,高伟,仓怀兴,毕汝昌. 福氏痢疾杆菌组氨酸合成中双功能焦磷酸水解酶和磷酸核糖环化水解酶双功能蛋白的初步研究[J]. 中国生物工程杂志, 2009, 29(04): 56-60.

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https://manu60.magtech.com.cn/biotech/CN/Y2009/V29/I04/56

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