Department of Pharmaceutical Technology & Biochemistry, Gdańsk University of Technology, 11/12 Narutowicza St., 80-233, Gdańsk, Poland.
Mycopathologia. 2010 Dec;170(6):397-402. doi: 10.1007/s11046-010-9337-y. Epub 2010 Jun 23.
Two genes, LYS21 and LYS22, encoding isoforms of homocitrate synthase, an enzyme catalysing the first committed step in the lysine biosynthetic pathway, were disrupted in Candida albicans using the SAT1 flipper strategy. The double null lys21Δ/lys22Δ mutant lacked homocitrate synthase activity and exhibited lysine auxotrophy in minimal media that could be fully rescued by the addition of 0.5-0.6 mM L: -lysine. On the other hand, its virulence in vivo in the model of disseminated murine candidiasis appeared identical to that of the mother, wild-type strain. These findings strongly question a possibility of exploitation of homocitrate synthase and possibly also other enzymes of the lysine biosynthetic pathway as targets in chemotherapy of disseminated fungal infections.
两个基因,LYS21 和 LYS22,编码同型柠檬酸合酶的同工型,该酶催化赖氨酸生物合成途径中的第一步,在白色念珠菌中使用 SAT1 flipper 策略被破坏。双缺失 lys21Δ/lys22Δ 突变体缺乏同型柠檬酸合酶活性,并在最小培养基中表现出赖氨酸营养缺陷,可通过添加 0.5-0.6 mM L: -赖氨酸完全挽救。另一方面,它在体内传播性鼠念珠菌病模型中的毒力与母株野生型菌株相同。这些发现强烈质疑将同型柠檬酸合酶和可能还有其他赖氨酸生物合成途径的酶作为靶向药物用于治疗播散性真菌感染的可能性。