Development Center for Biotechnology, 81 Chang Hsing Street, Taipei, Taiwan, ROC.
World J Microbiol Biotechnol. 1990 Jun;6(2):127-43. doi: 10.1007/BF01200932.
Pseudomonas sp. strains, isolated from soil, utilized toluene as their sole carbon source through ameta cleavage pathway. Strains metabolizing toluene through anortho cleavage pathway were selected from the wild typemeta strain. Theortho pathway strains were subjected to chemostat selection to obtain a fast-growing strain with doubling time reduced from 14 to 1.2 h. Benzoale and antibiotics enrichment selection procedures were utilized to select a blocked mutant. The blocked mutant grew on acetate as its sole carbon source and oxidatively converted toluene tocis, cis-muconic acid. Double-blocked and muconate-permeable mutants were also selected to reduce reversion frequency and to enhance muconic acid production. In shake-flask experiments, muconic acid at 3.5 g/l was obtained after 2 days of fermentation. In a 14 l fermenter, muconic acid was produced at 45 g/l in 4 days of controlled fed-batch fermentation. The oxidative bioconversion process was also demonstrated in a 1500 l fermenter.
从土壤中分离出的假单胞菌菌株通过 meta 裂解途径将甲苯用作唯一的碳源。从野生型 meta 菌株中选择通过邻位裂解途径代谢甲苯的菌株。将邻位途径菌株进行恒化器选择,以获得倍增时间从 14 小时缩短至 1.2 小时的快速生长菌株。利用苯并酸盐和抗生素富集选择程序选择受阻突变体。受阻突变体可以以乙酸盐作为唯一碳源生长,并将甲苯氧化转化为顺式,顺式-粘康酸。还选择了双重受阻和粘康酸通透突变体,以降低回复频率并提高粘康酸产量。在摇瓶实验中,经过 2 天的发酵可得到 3.5 g/L 的粘康酸。在 14 L 发酵罐中,通过 4 天的控制补料分批发酵可生产 45 g/L 的粘康酸。在 1500 L 发酵罐中也证明了氧化生物转化过程。