Kim Seung-Rak, Kang Hyeon-Woo, Ro Hyeon-Su
Department of Microbiology and Research Institute of Life Sciences, Gyeongsang National University, Jinju 660-701, Korea.
Mycobiology. 2013 Sep;41(3):159-63. doi: 10.5941/MYCO.2013.41.3.159. Epub 2013 Sep 30.
A chemical mutagenesis technique was employed for development of mutant strains of Sparassis crispa targeting the shortened cultivation time and the high β-glucan content. The homogenized mycelial fragments of S. crispa IUM4010 strain were treated with 0.2 vol% methyl methanesulfonate, an alkylating agent, yielding 199 mutant strains. Subsequent screening in terms of growth and β-glucan content yielded two mutant strains, B4 and S7. Both mutants exhibited a significant increase in β-glucan productivity by producing 0.254 and 0.236 mg soluble β-glucan/mg dry cell weight for the B4 and S7 strains, respectively, whereas the wild type strain produced 0.102 mg soluble β-glucan/mg dry cell weight. The results demonstrate the usefulness of chemical mutagenesis for generation of mutant mushroom strains.
采用化学诱变技术培育皱盖乌芝突变菌株,目标是缩短培养时间并提高β-葡聚糖含量。用0.2体积%的甲磺酸甲酯(一种烷基化剂)处理皱盖乌芝IUM4010菌株的匀浆菌丝片段,得到199个突变菌株。随后根据生长情况和β-葡聚糖含量进行筛选,得到两个突变菌株B4和S7。两个突变菌株的β-葡聚糖产量均显著增加,B4菌株和S7菌株分别产生0.254和0.236毫克可溶性β-葡聚糖/毫克干细胞重量,而野生型菌株产生0.102毫克可溶性β-葡聚糖/毫克干细胞重量。结果表明化学诱变对于产生蘑菇突变菌株是有用的。