Xie Zhangzhang, Lin Weitie, Luo Jianfei
Guangdong Key Laboratory of Fermentation and Enzyme Engineering, College of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510006, China.
Biomed Res Int. 2017;2017:6304248. doi: 10.1155/2017/6304248. Epub 2017 Jul 17.
sp. PR1 is a xylanolytic and agarolytic bacterium isolated from the Pearl River. Strain PR1 is closely related to and (identity > 98%). The xylanase and agarase contents of strain PR1 reach up to 15.4 and 25.9 U/mL, respectively. The major cellular fatty acids consisted of C16:0 (36.7%), C18:0 (8.8%), C20:0 (6.8%), C iso 2-OH or/and C7c (17.4%), and C7c or/and C6c (6.7%). A total of 251 CAZyme modules (63 CBMs, 20 CEs, 128 GHs, 38 GTs, and 2 PLs) were identified from 3,730 predicted proteins. Genomic analysis suggested that strain PR1 has a complete xylan-hydrolyzing (5 -xylanases, 16 -xylosidases, 17 -arabinofuranosidases, 9 acetyl xylan esterases, 4 -glucuronidases, and 2 ferulic acid esterases) and agar-hydrolyzing enzyme system (2 -agarases and 2 -neoagarooligosaccharide hydrolases). In addition, the main metabolic pathways of xylose, arabinose, and galactose are established in the genome-wide analysis. This study shows that strain PR1 contains a large number of glycoside hydrolases.
sp. PR1是从珠江分离出的一种能分解木聚糖和琼脂的细菌。菌株PR1与[具体菌株1]和[具体菌株2]密切相关(相似度>98%)。菌株PR1的木聚糖酶和琼脂酶含量分别高达15.4和25.9 U/mL。主要的细胞脂肪酸由C16:0(36.7%)、C18:0(8.8%)、C20:0(6.8%)、C iso 2-OH或/和C7c(17.4%)以及C7c或/和C6c(6.7%)组成。从3730个预测蛋白中鉴定出总共251个碳水化合物活性酶模块(63个碳水化合物结合模块、20个碳水化合物酯酶、128个糖苷水解酶、38个糖基转移酶和2个多糖裂解酶)。基因组分析表明,菌株PR1具有完整的木聚糖水解酶系统(5个木聚糖酶、16个木糖苷酶、17个阿拉伯呋喃糖苷酶、9个乙酰木聚糖酯酶、4个葡萄糖醛酸酶和2个阿魏酸酯酶)和琼脂水解酶系统(2个琼脂酶和2个新琼脂寡糖水解酶)。此外,在全基因组分析中建立了木糖、阿拉伯糖和半乳糖的主要代谢途径。本研究表明,菌株PR1含有大量的糖苷水解酶。