Paliy Oleg, Gunasekera Thusitha S
Department of Biochemistry and Molecular Biology, Wright State University, 256 BioSciences, 3640 Col. Glenn Hwy, Dayton, OH 45435, USA.
Appl Microbiol Biotechnol. 2007 Jan;73(5):1169-72. doi: 10.1007/s00253-006-0554-8. Epub 2006 Aug 30.
Escherichia coli strain BL21 is commonly used as a host strain for protein expression and purification. For structural analysis, proteins are frequently isotopically labeled with deuterium (2H), 13C, or 15N by growing E. coli cultures in a medium containing the appropriate isotope. When large quantities of fully deuterated proteins are required, E. coli is often grown in minimal media with deuterated succinate or acetate as the carbon source because these are less expensive. Despite the widespread use of BL21, we found no data on the effect of different minimal media and carbon sources on BL21 growth. In this study, we assessed the growth behavior of E. coli BL21 in minimal media with different gluconeogenic carbon sources. Though BL21 grew reasonably well on glycerol and pyruvate, it had a prolonged lag-phase on succinate (20 h), acetate (10 h), and fumarate (20 h), attributed to the physiological adaptation of E. coli cells. Wild-type strain NCM3722 (K12) grew well on all the substrates. We also examined the growth of E. coli BL21 in minimal media that differed in their salt composition but not in their source of carbon. The commonly used M9 medium did not support the optimum growth of E. coli BL21 in minimal medium. The addition of ferrous sulphate to M9 medium (otherwise lacking it) increased the growth rate of E. coli cultures and significantly increased their cell density in the stationary phase.
大肠杆菌BL21菌株通常用作蛋白质表达和纯化的宿主菌株。对于结构分析,通过在含有适当同位素的培养基中培养大肠杆菌培养物,蛋白质经常用氘(2H)、13C或15N进行同位素标记。当需要大量完全氘代的蛋白质时,大肠杆菌通常在以氘代琥珀酸盐或乙酸盐作为碳源的基本培养基中生长,因为这些更便宜。尽管BL21被广泛使用,但我们未找到关于不同基本培养基和碳源对BL21生长影响的数据。在本研究中,我们评估了大肠杆菌BL21在含有不同糖异生碳源的基本培养基中的生长行为。尽管BL21在甘油和丙酮酸上生长良好,但在琥珀酸盐(20小时)、乙酸盐(10小时)和富马酸盐(20小时)上有延长的滞后期,这归因于大肠杆菌细胞的生理适应。野生型菌株NCM3722(K12)在所有底物上都生长良好。我们还研究了大肠杆菌BL21在盐组成不同但碳源相同的基本培养基中的生长情况。常用的M9培养基不支持大肠杆菌BL21在基本培养基中的最佳生长。向M9培养基中添加硫酸亚铁(否则缺乏硫酸亚铁)可提高大肠杆菌培养物的生长速率,并显著增加其在稳定期的细胞密度。