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在重复分批发酵中,用于生物质 - 胞外多糖 - 胞内多糖的三联总生产及其抗口腔癌β - 葡聚糖反应的颗粒直径。

Pellet diameter of in a repeated-batch fermentation for the trio total production of biomass-exopolysaccharide-endopolysaccharide and its anti-oral cancer beta-glucan response.

作者信息

Abdullah Nur Raihan, Sharif Faez, Azizan Nur Hafizah, Hafidz Ismail Fitri Mohd, Supramani Sugenendran, Usuldin Siti Rokhiyah Ahmad, Ahmad Rahayu, Wan-Mohtar Wan Abd Al Qadr Imad

机构信息

Functional Omics and Bioprocess Development Laboratory, Institute of Biological Sciences, Faculty of Science, Universiti of Malaya, 50603, Kuala Lumpur, Malaysia.

Department of Biotechnology, Kulliyyah of Science, International Islamic University Malaysia, 25200 Kuantan, Pahang, Malaysia.

出版信息

AIMS Microbiol. 2020 Oct 22;6(4):379-400. doi: 10.3934/microbiol.2020023. eCollection 2020.

DOI:10.3934/microbiol.2020023
PMID:33364534
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7755588/
Abstract

The pellet morphology and diameter range (DR) of were observed in a repeated-batch fermentation (RBF) for the trio total production of biomass, exopolysaccharide (EPS) and endopolysaccharide (ENS). Two factors were involved in RBF; broth replacement ratio (BRR: 60%, 75% and 90%) and broth replacement time point (BRTP: log, transition and stationary phase) in days. In RBF, 34.31 g/L of biomass favoured small-compact pellets with DR of 20.67 µm< d < 24.00 µm (75% BRR, day 11 of BRTP). EPS production of 4.34 g/L was prone to ovoid-starburst pellets with DR of 34.33 µm< d <35.67 µm (75% BRR, day 13 of BRTP). Meanwhile, the highest 2.43 g/L of ENS production favoured large-hollow pellets with DR of 34.00 µm< d < 38.67 µm (90% BRR, day 13 of BRTP). In addition, RBF successfully shortened the biomass-EPS-ENS fermentation period (31, 33 and 35 days) from batch to 5 days, in seven consecutive cycles of RBF. In a FTIR detection, β-glucan (BG) from EPS and ENS extracts were associated with β-glycosidic linkages (2925 cm, 1635 cm, 1077 cm, 920 cm and 800 cm wavelengths) with similar H NMR spectral behaviour (4.58, 3.87 and 3.81 ppm). Meanwhile, 4 mg/L of BG gave negative cytotoxic effects on normal gingival cell line (hGF) but induced antiproliferation (IC = 0.23 mg/mL) against cancerous oral Asian cellosaurus cell line (ORL-48). Together, this study proved that mycelial pellets could withstand seven cycles of long fermentation condition and possessed anti-oral cancer beta-glucan, which suits large-scale natural drug fermentation.

摘要

在重复批次发酵(RBF)中观察了 的颗粒形态和直径范围(DR),以实现生物质、胞外多糖(EPS)和胞内多糖(ENS)的三联总生产。RBF涉及两个因素;肉汤替换率(BRR:60%、75%和90%)和肉汤替换时间点(BRTP:对数期、过渡期和稳定期,以天数计)。在RBF中,34.31 g/L的生物质有利于形成小而紧密的颗粒,DR为20.67 µm < d < 24.00 µm(75% BRR,BRTP第11天)。4.34 g/L的EPS产量倾向于形成卵形星爆颗粒,DR为34.33 µm < d < 35.67 µm(75% BRR,BRTP第13天)。同时,最高2.43 g/L的ENS产量有利于形成大的中空颗粒,DR为34.00 µm < d < 38.67 µm(90% BRR,BRTP第13天)。此外,RBF成功地将生物质-EPS-ENS发酵周期(31、33和35天)从分批发酵缩短至5天,在RBF的七个连续周期中实现。在傅里叶变换红外光谱(FTIR)检测中,EPS和ENS提取物中的β-葡聚糖(BG)与β-糖苷键(波长为2925 cm、1635 cm、1077 cm、920 cm和800 cm)相关,具有相似的氢核磁共振(1H NMR)光谱行为(4.58、3.87和3.81 ppm)。同时,4 mg/L的BG对正常牙龈细胞系(hGF)具有阴性细胞毒性作用,但对口腔癌亚洲细胞系(ORL-48)具有抗增殖作用(IC50 = 0.23 mg/mL)。总之,本研究证明 菌丝球能够承受七个周期的长时间发酵条件,并拥有抗口腔癌的β-葡聚糖,适合大规模天然药物发酵。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/507fc5470b60/microbiol-06-04-023-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/859ca5b5e214/microbiol-06-04-023-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/e161736a66d0/microbiol-06-04-023-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/2f196ea27dba/microbiol-06-04-023-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/70e714bac224/microbiol-06-04-023-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/375ecd55c609/microbiol-06-04-023-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/03b8ece26526/microbiol-06-04-023-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/73771349033f/microbiol-06-04-023-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/507fc5470b60/microbiol-06-04-023-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/859ca5b5e214/microbiol-06-04-023-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/e161736a66d0/microbiol-06-04-023-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/2f196ea27dba/microbiol-06-04-023-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/70e714bac224/microbiol-06-04-023-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/375ecd55c609/microbiol-06-04-023-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/03b8ece26526/microbiol-06-04-023-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/73771349033f/microbiol-06-04-023-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f5f/7755588/507fc5470b60/microbiol-06-04-023-g008.jpg

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