Isolation of ethanol- and acid-resistant Acinetobacter baumannii from daqu for efficient esterification of acidic
Jiacheng Li1, Yuan Zou1, Yumei Jiang1
1School of Food and Liquor Engineering, Sichuan University of Science & Engineering, Yinbin, China.
Abstract:
A large amount of highly acidic wastewater, known as Huangshui, is produced during liquor brewing. To improve its utilization rate and achieve resource recovery of liquor by-products. A strain with high esterifying ability was screened from Daqu and identified as Acinetobacter baumannii. The strain exhibited an esterification enzyme activity of (16.79 ± 0.03) U/mL and an esterification capacity of (45.37 ± 0.33) mg/g. It was able to grow normally under conditions of 7% ethanol and pH 4.0, demonstrating strong acid and ethanol tolerance, indicating its potential for preparing a Huangshui esterification solution. Subsequently, Huangshui was esterified using ethanol, caproic acid and Daqu powder prepared with this strain. Analysis of trace components in Huangshui before and after esterification showed that the ethyl caproate content in the esterified Huangshui reached (649.26 ± 2.39) mg/L, which was 13.19 times higher than that before esterification, while ethyl lactate decreased by 15.35%. These results indicate a notable ability to enhance ethyl caproate and reduce ethyl lactate. It is expected that the application of this Huangshui esterification solution could improve the flavor and quality of Non-gxiangxing Baijiu by increasing ethyl caproate and decreasing ethyl lactate, thus providing a reliable experimental basis for the resource utilization of Huangshui.
More Related Videos
08:37The Application of Open Searching-based Approaches for the Identification of Acinetobacter baumannii O-linked Glycopeptides
Published on: November 2, 2021
08:21Isolation and Screening from Soil Biodiversity for Fungi Involved in the Degradation of Recalcitrant Materials
Published on: May 16, 2022
Related Concept Videos
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Acid Halides to Esters: Alcoholysis
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
