Saika Azusa, Koike Hideaki, Yarimizu Tohru, Watanabe Takashi, Kitamoto Hiroko, Morita Tomotake
Research Institute for Sustainable Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 5-2, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8565, Japan.
Bioproduction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba Central 6-9, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8566, Japan.
AMB Express. 2019 Jul 6;9(1):100. doi: 10.1186/s13568-019-0825-2.
The basidiomycetous yeast Pseudozyma antarctica (currently designated Moesziomyces antarcticus) produces extracellular enzymes and glycolipids, including mannosylerythritol lipids (MELs), which are biosurfactants. Strain GB-4(0) of this species was previously isolated from rice husks and produces biodegradable plastic-degrading enzyme (Pseudozyma antarctica esterase; PaE). In this study, we generated a MEL biosynthesis-deficient strain (∆PaEMT1) by deleting the gene PaEMT1, which is essential to MEL biosynthesis in strain GB-4(0). The resulting ∆PaEMT1 strain showed deficient PaE activity, and the corresponding signal was hardly detected in its culture supernatant through western blotting analysis using rabbit anti-PaE serum. On the other hand, the relative expression of the gene PaCLE1, encoding PaE, was identical between GB-4(0) and ∆PaEMT1 based on quantitative real-time PCR. When strain ∆PaEMT1 was grown in culture media supplemented with various surfactants, i.e., Tween20, BRIJ35 and TritonX-100, and MELs, PaE activity and secretion recovered. We also attempted to detect intracellular PaE using cell-free extract, but observed no signal in the soluble or insoluble fractions of ∆PaEMT1. This result suggested that the PaCLE1 gene was not translated to PaE, or that expressed PaE was degraded immediately in ∆PaEMT1. Based on these results, MEL biosynthesis is an important contributor to PaE production.
担子菌酵母南极假丝酵母(目前命名为南极莫氏酵母)能产生细胞外酶和糖脂,包括甘露糖赤藓糖醇脂(MELs),这些都是生物表面活性剂。该物种的GB-4(0)菌株先前从稻壳中分离得到,可产生可生物降解塑料的降解酶(南极假丝酵母酯酶;PaE)。在本研究中,我们通过缺失对GB-4(0)菌株中MEL生物合成至关重要的PaEMT1基因,构建了一个MEL生物合成缺陷菌株(∆PaEMT1)。所得的∆PaEMT1菌株显示出PaE活性缺陷,并且通过使用兔抗PaE血清的蛋白质印迹分析,在其培养上清液中几乎检测不到相应信号。另一方面,基于定量实时PCR,编码PaE的PaCLE1基因在GB-4(0)和∆PaEMT1之间的相对表达是相同的。当∆PaEMT1菌株在补充有各种表面活性剂(即吐温20、BRIJ35和曲拉通X-100)和MELs的培养基中生长时,PaE活性和分泌得以恢复。我们还尝试使用无细胞提取物检测细胞内的PaE,但在∆PaEMT1的可溶性或不溶性部分均未观察到信号。该结果表明,PaCLE1基因未翻译成PaE,或者在∆PaEMT1中表达的PaE立即被降解。基于这些结果,MEL生物合成是PaE产生的一个重要因素。