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Xiaoyan Liu,Jinshun Lv,Jiaxing Xu,Jun Xia,Benlin Dai,Xiangqian Xu,Jiming Xu 한국식품과학회 2017 Food Science and Biotechnology Vol.26 No.4
Mutants of Yarrowia lipolytica with high erythritol production were generated through an atmospheric and room temperature plasma (ARTP) mutation system. Among these mutants, Y. lipolytica M53 exhibited the highest erythritol yield. In a batch culture, M53 produced 64.8 g/L erythritol from 100 g/L glycerol. The yields of byproducts (e.g. mannitol, arabitol, and a-ketoglutaric acid) were low, and the mechanisms underlying these changes were examined by measuring enzyme activities in the pentose phosphate pathway. Up to 145.2 g/L erythritol was produced by M53 from 200 g/L of glycerol, and erythritol accumulation was promoted by 3.7 mg/L of Cu2?, 10.15 mg/L of Mn2?, and 30.37 g/L of NaCl. Fed-batch cultivation of M53 in a 5-L fermentor produced 169.3 g/L erythritol with low levels of byproducts within 168 h. This finding confirmed the potential of M53 as an erythritol producer on a commercial scale.
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Dehydration reaction of bio-ethanol to ethylene over modified SAPO catalysts
Yu Chen,Ling Tao,Bin Dai,Mingde Yang,Zhen Chen,Xiaoyan Zhu,Yulong Wu 한국공업화학회 2010 Journal of Industrial and Engineering Chemistry Vol.16 No.5
Mnmodified SAPO-11 (Mn-SAPO-11), Zn-SAPO-11, Mn-SAPO-34 and Zn-SAPO-34 were first synthesized with hydrothermal method in the laboratory. Dehydration of ethanol to ethylene over SAPO-11, SAPO-34and four materials above as catalysts was carried out and Mn-SAPO-34 exhibited the best conversion and selectivity (99.35% and 98.44%, respectively) at 340 8C. The introduction of Mn2+ or Zn2+ into the SAPO channel generated in Mn-SAPO or Zn-SAPO samples was proved by X-ray diffraction (XRD), scanning electron microscopy (SEM) and nitrogen adsorption. NH3-TPD study revealed that modification of Mn2+or Zn2+ in the SAPO framework led to increase the weak acid strength and give rise to weak acid sites. The effects of operation parameters, such as loading amount, modification methods, reaction time, reaction temperature, mass space velocity and concentration of ethanol have also been investigated experimentally. 2010 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
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Gang Wang,Baisha Ouyang,Fang Jing,Xiaoyan Dai 대한약리학회 2023 The Korean Journal of Physiology & Pharmacology Vol.27 No.1
The poor outcome of advanced ovarian cancer under conventional therapy necessitates new strategies to improve therapeutic efficacy. β-glucosidase (encoded by GBA) is a lysosomal enzyme and is involved in sphingolipids metabolism. Recent studies revealed that β-glucosidase plays a role in cancer development and chemoresistance. In this work, we systematically evaluated the expression and role of GBA in ovarian cancer. Our work demonstrates that inhibition of β-glucosidase has therapeutic potential for ovarian cancer. Gene Expression Profiling Interactive Analysis database, western blot and immunohistochemistry analyses of patient samples demonstrated that GBA mRNA and protein expression levels were significantly increased in ovarian cancer compared to normal tissues. Functional studies using gainof- function and loss-of-function approaches demonstrated that GBA overexpression did not affect growth and migration but alleviated cisplatin’s efficacy in ovarian cancer cells. In addition, GBA depletion resulted in growth inhibition, apoptosis induction, and enhancement of cisplatin’s efficacy. Of note, we found that GBA inhibition specifically decreased receptor tyrosine kinase AXL level, leading to the suppression of AXL-mediated signaling pathways. Our data suggest that GBA represents a promising target to inhibit AXL signaling and overcome cisplatin resistance in ovarian cancer.
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