Penkhrue Watsana, Kanpiengjai Apinun, Khanongnuch Chartchai, Masaki Kazuo, Pathom-Aree Wasu, Punyodom Winita, Lumyong Saisamorn
a Department of Biology , Faculty of Science, Chiang Mai University, Muang District , Chiang Mai , Thailand.
b Division of Biotechnology, School of Agro-Industry, Faculty of Agro-Industry, Chiang Mai University, Muang District , Chiang Mai , Thailand.
Prep Biochem Biotechnol. 2017 Aug 9;47(7):730-738. doi: 10.1080/10826068.2017.1315597. Epub 2017 Apr 17.
This study aims to find the optimal medium and conditions for polylactic acid (PLA)-degrading enzyme production by Amycolatopsis sp. SCM_MK2-4. Screening of the most effective components in the enzyme production medium by Plackett-Burman design revealed that the silk cocoon and PLA film were the most significant variables enhancing the PLA-degrading enzyme production. After an response surface methodology, a maximum amount of PLA-degrading enzyme activity at 0.74 U mL was predicted and successfully validated at 95% after 0.39% (w/v) silk cocoon and 1.62% (w/v) PLA film were applied to the basal medium. The optimal initial pH value, temperature, and inoculum size were evaluated by a method considering one-factor-at-a-time. The values were recorded at an initial pH in the range of 7.5-9.0, a temperature of 30-32°C, and an inoculum size of 4-10%. The highest activity of approximately 0.95 U mL was achieved after 4 days of cultivation using the optimized medium and under optimized conditions in a shake flask. Upscaling to the use of a 3-L stirred tank fermenter was found to be successful with a PLA-degrading activity of 5.53 U mL; which represents a 51-fold increase in the activity compared with that obtained from the nonoptimized medium and conditions in the shake flask.
本研究旨在寻找拟无枝酸菌SCM_MK2 - 4产生聚乳酸(PLA)降解酶的最佳培养基和条件。通过Plackett - Burman设计筛选酶生产培养基中最有效的成分,结果表明蚕茧和PLA薄膜是提高PLA降解酶产量的最显著变量。经过响应面法,预测在基础培养基中添加0.39%(w/v)蚕茧和1.62%(w/v)PLA薄膜后,PLA降解酶活性的最大值为0.74 U/mL,并在95%的置信度下成功验证。通过一次只考虑一个因素的方法评估了最佳初始pH值、温度和接种量。记录的值为初始pH值在7.5 - 9.0范围内,温度为30 - 32°C,接种量为4 - 10%。在摇瓶中使用优化培养基并在优化条件下培养4天后,获得了约0.95 U/mL的最高活性。扩大规模至使用3-L搅拌罐发酵罐取得成功,PLA降解活性为5.53 U/mL;与在摇瓶中使用未优化的培养基和条件所获得的活性相比,活性提高了51倍。