Kumar Dhirendra, Dubey Kashyap Kumar
Microbial Biotechnology Laboratory, University Institute of Engineering and Technology, Maharshi Dayanand University Rohtak, Rohtak, Haryana, 124001, India.
Department of Biotechnology, Central University of Haryana, Jant-Pali, Mahendergarh, Haryana, 123031, India.
3 Biotech. 2017 Jul;7(3):157. doi: 10.1007/s13205-017-0759-9. Epub 2017 Jun 16.
Betulinic acid as a derivative of betulin is widely reported for its anti-HIV and antitumor activities. Betulin has three most significant positions, i.e., primary hydroxyl group at position C-28, secondary hydroxyl group at position C-3, and alkene moiety at position C-20, where chemical modifications were performed to yield pharmacologically more active derivatives. Bioconversion optimization was performed for the enhancement in the percentage of conversion using statistical approach by opting temperature, pH and betulin concentration as independent variables. Three hundred fifty isolates were screened from natural sources under selective medium containing up to 3 g/l of betulin for their tolerance and bioconversion efficiency. Isolate KD235 was found to grow in 3 g/l betulin with 23.34 ± 0.57 g/l biomass and 0.67 ± 0.06 g/l betulinic acid production. New isolate KD235 was characterized by molecular analysis and named as Bacillus megaterium KD235. Molecular characterization of a potentially active isolate for the transformation of betulin to betulinic acid was suggested as isolate Bacillus megaterium KD235. Maximum bioconversion (22 ± 1.5%) was found at optimized conditions, i.e., pH 6.5, temperature 30 °C and at 3 g/l betulin. Validations of experiments as ~11% more bioconversion i.e., 1 ± 0.1 g/l betulinic acid were obtained using 5 l lab fermenter as compared to shake flask.
桦木酸作为桦木醇的衍生物,因其抗HIV和抗肿瘤活性而被广泛报道。桦木醇有三个最重要的位置,即C-28位的伯羟基、C-3位的仲羟基和C-20位的烯烃部分,可对这些位置进行化学修饰以产生药理活性更强的衍生物。通过选择温度、pH值和桦木醇浓度作为自变量,采用统计方法进行生物转化优化,以提高转化率。在含有高达3 g/l桦木醇的选择性培养基中,从天然来源筛选了350株菌株,检测它们的耐受性和生物转化效率。发现菌株KD235能在3 g/l桦木醇中生长,生物量为23.34±0.57 g/l,桦木酸产量为0.67±0.06 g/l。新菌株KD235通过分子分析进行了表征,并命名为巨大芽孢杆菌KD235。建议将潜在活性菌株巨大芽孢杆菌KD235作为将桦木醇转化为桦木酸的菌株进行分子表征。在优化条件下,即pH 6.5、温度30℃和桦木醇浓度为3 g/l时,发现最大生物转化率为(22±1.5%)。与摇瓶相比,使用5 l实验室发酵罐进行实验验证,生物转化率提高了约11%,即桦木酸产量为1±0.1 g/l。