Wu Shan, Lu Hong-Yun, Chen Qi-He, Xie Hui-Chun, Jiao Ying-Chun
College of Agriculture and Animal Husbandry, Qinghai University, No.251 Ningda Road, Xining, 810016, Qinghai, China.
Department of Food Science and Nutrition, Zhejiang University, 154 Yugu Road, Hangzhou, 310058, Zhejiang, China.
Bioprocess Biosyst Eng. 2021 Nov;44(11):2303-2313. doi: 10.1007/s00449-021-02605-8. Epub 2021 Jul 23.
Agaricus bitorquis (Quél.) Sacc. Chaidam (ABSC) is a wild edible fungus uniquely found in the Tibet Plateau. ABSC is rich in polysaccharides that are considered biologically active. This study aimed to determine the feasibility of enhancing exopolysaccharide (EPS) production by ABSC in shake flask culture by supplementing the fermentation medium with anthocyanin extract. Different concentrations of Lycium ruthenicum Murr. (LRM) anthocyanin crude extract were tested on ABSC fermentation. The activity of phosphoglucose isomerase (PGI), phosphoglucose mutase (PGM), and phosphomannose isomerase (PMI), enzymes presumably involved in EPS synthesis by ABSC, was determined. ABSC transcriptomic profile in response to the presence of anthocyanins during fermentation was also investigated. LRM anthocyanin crude extract (0.06 mg/mL) was most effective in increasing EPS content and mycelial biomass (by 208.10% and 105.30%, respectively, P < 0.01). The activity of PGI, PGM, and PMI was increased in a medium where LRM anthocyanin extract and its main components (proanthocyanidins and petunia anthocyanin) were added. RNA-Seq analysis showed that 349 genes of ABSC were differentially expressed during fermentation in the medium containing anthocyanin extract of LRM; 93 genes were up-regulated and 256 genes down-regulated. From gene ontology enrichment analysis, differentially expressed genes were mostly assigned to carbohydrate metabolism and signal transduction categories. Collectively, LRM anthocyanins extract positively affected EPS production and mycelial biomass during ABSC fermentation. Our study provides a novel strategy for improving EPS production and mycelial growth during ABSC liquid submerged fermentation.
双孢蘑菇(Agaricus bitorquis (Quél.) Sacc.)柴达木变种(ABSC)是青藏高原特有的一种野生可食用真菌。ABSC富含被认为具有生物活性的多糖。本研究旨在通过在摇瓶培养中向发酵培养基中添加花青素提取物来确定提高ABSC胞外多糖(EPS)产量的可行性。对不同浓度的黑果枸杞(LRM)花青素粗提物进行了ABSC发酵试验。测定了可能参与ABSC合成EPS的磷酸葡萄糖异构酶(PGI)、磷酸葡萄糖变位酶(PGM)和磷酸甘露糖异构酶(PMI)的活性。还研究了发酵过程中ABSC对花青素存在的转录组图谱。LRM花青素粗提物(0.06 mg/mL)在增加EPS含量和菌丝体生物量方面最有效(分别增加208.10%和105.30%,P < 0.01)。在添加了LRM花青素提取物及其主要成分(原花青素和矮牵牛花青素)的培养基中,PGI、PGM和PMI的活性增加。RNA测序分析表明,在含有LRM花青素提取物的培养基中发酵期间,ABSC有349个基因差异表达;93个基因上调,256个基因下调。从基因本体富集分析来看,差异表达基因大多被归类到碳水化合物代谢和信号转导类别。总体而言,LRM花青素提取物对ABSC发酵过程中的EPS产量和菌丝体生物量有积极影响。我们的研究为提高ABSC液体深层发酵过程中的EPS产量和菌丝体生长提供了一种新策略。