Wang Xiao-Ling, Ding Zhong-Yang, Zhao Yan, Liu Gao-Qiang, Zhou Guo-Ying
Hunan Provincial Key Laboratory for Forestry Biotechnology, College of Life Science and Technology, Central South University of Forestry & Technology, Changsha, P.R. China.
National Engineering Laboratory for Cereal Fermentation Technology, Jiangnan University, Wuxi, PR. China.
Int J Med Mushrooms. 2017;19(5):419-431. doi: 10.1615/IntJMedMushrooms.v19.i5.40.
Triterpene acids are among the major bioactive constituents of lucidum. However, submerged fermentation techniques for isolating triterpene acids from G. lucidum have not been optimized for commercial use, and the antitumor activity of the mycelial triterpene acids needs to be further proven. The aim of this work was to optimize the conditions for G. lucidum culture with respect to triterpene acid production, scaling up the process, and examining the in vitro antitumor activity of mycelial triterpene acids. The key conditions (i.e., initial pH, fermentation temperature, and rotation speed) were optimized using response surface methodology, and the in vitro antitumor activity was evaluated using the MTT method. The optimum key fermentation conditions for triterpene acid production were pH 6.0; rotation speed, 161.9 rpm; and temperature, 30.1°C, resulting in a triterpene acid yield of 291.0 mg/L in the validation experiment in a 5-L stirred bioreactor; this yield represented a 70.8% increase in titer compared with the nonoptimized conditions. Furthermore, the optimized conditions were then successfully scaled up to a production scale of 200 L, and a triterpene productivity of 47.9 mg/L/day was achieved, which is, to our knowledge, the highest reported in the large-scale fermentation of G. lucidum. In addition, the mycelial triterpene acids were found to be cytotoxic to the SMMC-7721 and SW620 cell lines in vitro. Chemical analysis showed that the key active triterpene acid compounds, ganoderic acids T and Me, predominated in the extract, at 69.2 and 41.6 mg/g, respectively. Thus, this work develops a simple and feasible batch fermentation technique for the large-scale production of antitumor triterpene acids from G. lucidum.
三萜酸是灵芝的主要生物活性成分之一。然而,从灵芝中分离三萜酸的深层发酵技术尚未针对商业用途进行优化,且菌丝体三萜酸的抗肿瘤活性有待进一步证实。本研究的目的是优化灵芝培养条件以提高三萜酸产量,扩大生产规模,并检测菌丝体三萜酸的体外抗肿瘤活性。采用响应面法对关键条件(即初始pH值、发酵温度和转速)进行优化,并使用MTT法评估体外抗肿瘤活性。三萜酸生产的最佳关键发酵条件为pH 6.0、转速161.9 rpm、温度30.1°C,在5 L搅拌式生物反应器的验证实验中,三萜酸产量达到291.0 mg/L;与未优化条件相比,该产量的效价提高了70.8%。此外,优化后的条件随后成功扩大到200 L的生产规模,三萜酸生产率达到47.9 mg/L/天,据我们所知,这是灵芝大规模发酵中报道的最高生产率。此外,发现菌丝体三萜酸在体外对SMMC - 7721和SW620细胞系具有细胞毒性。化学分析表明,提取物中的关键活性三萜酸化合物灵芝酸T和灵芝酸Me分别占主导地位,含量分别为69.2和41.6 mg/g。因此,本研究开发了一种简单可行的分批发酵技术,用于从灵芝中大规模生产抗肿瘤三萜酸。