Institute for Agro-environmental Sciences, National Agriculture and Food Research Organization (NARO), Tsukuba, Japan.
Biosci Biotechnol Biochem. 2020 May;84(5):1077-1087. doi: 10.1080/09168451.2020.1713718. Epub 2020 Jan 20.
Fungi play an important role in the degradation of biodegradable plastics (BPs) in soil. However, little is known about their dynamics in the soil during the degradation of BPs. We studied the community dynamics of BP-degrading fungi during poly(butylene succinateadipate) (PBSA) film degradation in two different types of soils using culture-dependent and culture-independent methods. The Fluvisol and the Andosol soils degrade embedded PBSA films at high and low speeds, respectively. The number of PBSA emulsion-degrading fungi that increased in the Fluvisol soil was higher than that in the Andosol soil after embedding with PBSA films. We succeeded in detecting internal transcribed spacer 1 (ITS1) regions those matched that of the fungi by polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) in both soils. Our results suggest that fungal community analyses using PCR-DGGE in combination with BP degraders isolation techniques enables the monitoring of BP films-degrading fungi.
真菌在土壤中可生物降解塑料(BPs)的降解中发挥着重要作用。然而,对于它们在 BPs 降解过程中在土壤中的动态变化却知之甚少。我们使用依赖培养和非依赖培养的方法研究了聚丁二酸丁二醇酯(PBSA)薄膜在两种不同类型土壤中的降解过程中,BP 降解真菌的群落动态。在 Fluvisol 和 Andosol 土壤中,嵌入 PBSA 薄膜的降解速度分别较快和较慢。在 Fluvisol 土壤中,与 PBSA 薄膜嵌入后相比,能够降解 PBSA 乳状液的真菌数量增加。我们通过聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)成功地在两种土壤中检测到了与真菌 ITS1 区相匹配的内部转录间隔区 1(ITS1)区域。我们的结果表明,使用 PCR-DGGE 结合 BP 降解菌分离技术进行真菌群落分析,可以监测 BP 薄膜降解真菌。