Abstract
The purpose of this study was to develop a method for detecting microbial activity based on soil esterase activity during biodegradation of polyester biodegradable mulch films after plowing the field. Herein, we report that the p-nitrophenyl butyrate (pNP–C4) substrate, among five pNP fatty acid substrates (pNP–acetate (C2), –C4, –hexanoate (C6), –decanoate (C10), and dodecanoate (C12)) in a cultivated field, is a specific indicator for detecting microbial activity associated with biodegradation of biodegradable polyesters. To evaluate film degradation by loss of weight and visual area, pieces of three different films were placed independently in meshed plastic bags and buried in a cultivated field in Japan, for seven months. One was made from poly(butylene succinate-co-adipate) (PBSA), and two were biodegradable polyester (poly(butylene terephthalate-co-adipate) and poly(butylene succinate)-type polymer)-based commercial films (hereafter described as films A and B) and weathered for three months in the cultivated field. The soil that adhered to the mesh bag and film was retrieved and mixed, and their esterase activities were measured using the five pNP fatty acid substrates. From the loss of visual area, the time taken from burial to accelerated degradation increased, in the order of PBSA, film A, and film B. The reproducibility of the hydrolytic activity values of pNP–C2, –C4, and –C6 in bulk soil were considered sufficient to measure baselines for the enzymatic activities. Among these substrates, the hydrolytic activity of pNP–C4 was significantly higher in the degradation process of PBSA and film A. In addition, unlike the pNP–C2 and –C6, the hydrolytic activity of the pNP–C4 in the bulk soil was not affected by changes in soil temperature and moisture under the conditions of this experiment. Therefore, the pNP–C4 hydrolytic activity can aid in the detection of the microbial activity associated with the biodegradation of polyester-based biodegradable mulch films in cultivated field soils.
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