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13th Annual Biotechnology Congress (BAC Madrid 2019): abstract collection
Authors:Ma  Wen-Tao  Liu  Qi  Ning  Meng-Xia  Qi  Yu-Xu  Rehman  Saad  Chen  De-Kun
Institution:1.Key Laboratory of Tobacco Biology and Processing, Tobacco Research Institute of Chinese Academy of Agricultural Sciences, Qingdao, 266101, People’s Republic of China
;2.CAS Key Laboratory of Biobased Materials, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, 266101, People’s Republic of China
;3.Haikou Cigar Research Institute, Hainan Provincial Branch of CNTC, Haikou, 571100, People’s Republic of China
;4.China Tobacco Standardization Research Center, Zhengzhou Tobacco Research Institute of CNTC, Zhengzhou, 450001, People’s Republic of China
;5.Research and Development Center, China Tobacco Anhui Industrial Co., Ltd., Hefei, 230088, People’s Republic of China
;
Abstract:Background

Tobacco stalk (TS), a major agricultural waste abundant in pectin, has resulted in concerns about the need for its reuse. The nicotine in TS is considered a chemical that is to\xic and hazardous to the environment.

Results

In this study, Bacillus tequilensis CAS-MEI-2-33 was isolated from cigar wrappers to produce alkaline pectinase using TS. Subsequently, the medium and fermentation conditions for the production of pectinase by B. tequilensis CAS-MEI-2-33 were optimized. The optimal fermentation period, pH of the initial fermentation medium, concentration of TS, and inoculum amount for B. tequilensis CAS-MEI-2-33 were 40 h, 40 g/L, 7.0, and 3%, respectively. Under optimal conditions, the pectinase activity was 1370 U/mL. Then, the enzymatic properties, such as the optimum pH, reaction temperature, temperature stability, and effects of metal ions, were studied. The optimal pH was determined to be 10.0, indicating that the enzyme was an alkaline pectinase. The optimal temperature was 40 °C, and pectinase activity was stable at 40 °C. The Ag+ metal ions were shown to remarkably promote enzyme activity. The pectinase was partly purified by ammonium sulfate precipitation, ion exchange chromatography, and Sephacryl S-100 chromatography. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and LC-MS/MS analyses were utilized to analyze the pectinase.

Conclusions

This study provided a new alkaline pectinase candidate and a new strategy for the use of TS.

Keywords:
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