Analysis of microbiomes in three traditional starters and volatile components of the Chinese rice wines

Chen Lihua,Ren Lixia,Dongna Li,Xia Ma 한국식품과학회 2021 Food Science and Biotechnology Vol.30 No.1

To understand the effect of microbial communityon the flavor of fermented rice wine, microbiomes inthree traditional starters (CMQ, NBQ, and YCQ) fromdifferent origins for making Chinese rice wines wereevaluated and the volatile components of their rice wineswere compared. The results showed that the dominantgenera in CMQ were Pantoea, Bacillus, Rhizopus, andCandida, the dominant microorganisms in NBQ were Pediococcus,Lactobacillus, Acetobacter, Weissella, Bacillus,Rhizopus, Candida, and Aspergillus, the dominantmicroorganisms in YCQ were Pediococcus, Lactobacillus,Leuconostoc, Weissella, Lactococcus, Ochrobactrum,Rhizopus, and Mucor. There were significant differences insensory properties of the wines brewed by three starters. Although the major aroma components were benzyl alcohol,2-octanone, benzoic acid, and phenethyl acetate, eachrice wine had its own main aroma components include1-octanol, 1-pentanol, ethyl acetate, etc. The resultsshowed that the different microbial communities in starterresults in the significant difference of the aroma componentsin its fermented rice wine.

Defining the N-Linked Glycosylation Site of Hantaan Virus Envelope Glycoproteins Essential for Cell Fusion

Zheng, Feng,Ma, Lixian,Shao, Lihua,Wang, Gang,Chen, Fengzhe,Zhang, Ying,Yang, Song The Microbiological Society of Korea 2007 The journal of microbiology Vol.45 No.1

The Hantaan virus (HTNV) is an enveloped virus that is capable of inducing low pH-dependent cell fusion. We molecularly cloned the viral glycoprotein (GP) and nucleocapsid (NP) cDNA of HTNV and expressed them in Vero E6 cells under the control of a CMV promoter. The viral gene expression was assessed using an indirect immunofluorescence assay and immunoprecipitation. The transfected Vero E6 cells expressing GPs, but not those expressing NP, fused and formed a syncytium following exposure to a low pH. Monoclonal antibodies (MAbs) against envelope GPs inhibited cell fusion, whereas MAbs against NP did not. We also investigated the N-linked glycosylation of HTNV GPs and its role in cell fusion. The envelope GPs of HTNV are modified by N-linked glycosylation at five sites: four sites on G1 (N134, N235, N347, and N399) and one site on G2 (N928). Site-directed mutagenesis was used to construct eight GP gene mutants, including five single N-glycosylation site mutants and three double-site mutants, which were then expressed in Vero E6 cells. The oligosaccharide chain on residue N928 of G2 was found to be crucial for cell fusion after exposure to a low pH. These results suggest that G2 is likely to be the fusion protein of HTNV.

One-Stage Anterolateral Debridement, Bone Grafting, and Internal Fixation for Treating Lumbosacral Tuberculosis

Tao Zhang,Lihua Ma,Xu Lan,Ping Zhen,Shiyong Wang,Zhilin Li 대한척추외과학회 2017 Asian Spine Journal Vol.11 No.2

Study Design: Retrospective case series. Purpose: To investigate the clinical efficacy and feasibility of one-stage anterolateral debridement, bone grafting, and internal fixation for treating lumbosacral tuberculosis. Overview of Literature: There has been no consensus regarding the optimal means of treating lumbosacral tuberculosis. The onestage anterolateral extraperitoneal approach for radical debridement, bone grafting, and internal fixation for treating lumbosacral tuberculosis is rare in literature. Methods: Twenty-one patients with lumbosacral tuberculosis were retrospectively analyzed. All patients underwent the surgery of anterolateral debridement after regularly antituberculous drugs therapy. We evaluated the erythrocyte sedimentation rate, C-reactive protein, radiography, computed tomography, magnetic resonance imaging, visual analogue score, and Oswestry disability index before and after surgery. Results: All patients completed a follow-up survey 9–48 months after surgery. All patients’ wounds healed well without chronic infection or sinus formation, and all patients with low-back pain reported relief after surgery. All cases had no tuberculosis recurrence. Solid bony fusion was achieved within 6–12 months. At final follow-up, evaluated the erythrocyte sedimentation rate decreased from 38.1±12.5 to 11.3±7.1 mm/hr, C-reactive protein decreased from 6.2±4.2 to 1.6±1.3 mg/dL, the visual analog scale score decreased from 4.6±1.1 to 1.4±1.0, the Oswestry disability index score decreased from 50.2%±11.9% to 13.0%±6.6%, and the lumbosacral angle increased from 20.0°±4.8° to 29.0°±3.9° (p <0.05). Conclusions: One-stage anterolateral debridement, bone grafting, and internal instrument fixation for treating lumbosacral tuberculosis is safe and effective.

Defining the N-Linked Glycosylation Site of Hantaan Virus Envelope Glycoproteins Essential for Cell Fusion

Feng Zheng,Lixian Ma,Lihua Shao,Gang Wang,Fengzhe Chen,Ying Zhang,Song Yang 한국미생물학회 2007 The journal of microbiology Vol.45 No.1

The Hantaan virus (HTNV) is an enveloped virus that is capable of inducing low pH-dependent cell fusion. We molecularly cloned the viral glycoprotein (GP) and nucleocapsid (NP) cDNA of HTNV and expressed them in Vero E6 cells under the control of a CMV promoter. The viral gene expression was assessed using an indirect immunofluorescence assay and immunoprecipitation. The transfected Vero E6 cells expressing GPs, but not those expressing NP, fused and formed a syncytium following exposure to a low pH. Monoclonal antibodies (MAbs) against envelope GPs inhibited cell fusion, whereas MAbs against NP did not. We also investigated the N-linked glycosylation of HTNV GPs and its role in cell fusion. The envelope GPs of HTNV are modified by N-linked glycosylation at five sites: four sites on G1 (N134, N235, N347, and N399) and one site on G2 (N928). Site-directed mutagenesis was used to construct eight GP gene mutants, including five single N-glycosylation site mutants and three double-site mutants, which were then expressed in Vero E6 cells. The oligosaccharide chain on residue N928 of G2 was found to be crucial for cell fusion after exposure to a low pH. These results suggest that G2 is likely to be the fusion protein of HTNV.

Dihydroartemisinin inhibits HepG2.2.15 proliferation by inducing cellular senescence and autophagy

( Jiang Zou ),( Qiang Ma ),( Ru Sun ),( Jiajing Cai ),( Hebin Liao ),( Lei Xu ),( Jingruo Xia ),( Guangcheng Huang ),( Lihua Yao ),( Yan Cai ),( Xiaowu Zhong ),( Xiaolan Guo ) 생화학분자생물학회(구 한국생화학분자생물학회) 2019 BMB Reports Vol.52 No.8

Dihydroartemisinin (DHA) has been reported to possess anti-cancer activity against many cancers. However, the pharmacologic effect of DHA on HBV-positive hepatocellular carcinoma (HCC) remains unknown. Thus, the objective of the present study was to determine whether DHA could inhibit the proliferation of HepG2.2.15 cells and uncover the underlying mechanisms involved in the effect of DHA on HepG2.2.15 cells. We found that DHA effectively inhibited HepG2.2.15 HCC cell proliferation both in vivo and in vitro. DHA also reduced the migration and tumorigenicity capacity of HepG2.2.15 cells. Regarding the underlying mechanisms, results showed that DHA induced cellular senescence by up-regulating expression levels of proteins such as p-ATM, p-ATR, γ-H₂AX, P53, and P21 involved in DNA damage response. DHA also induced autophagy (green LC3 puncta gathered together and LC3II/LC3I ratio increased through AKT-mTOR pathway suppression). Results also revealed that DHA-induced autophagy was not linked to senescence or cell death. TPP1 (telomere shelterin) overexpression could not rescue DHA-induced anticancer activity (cell proliferation). Moreover, DHA down-regulated TPP1 expression. Gene knockdown of TPP1 caused similar phenotypes and mechanisms as DHA induced phenotypes and mechanisms in HepG2.2.15 cells. These results demonstrate that DHA might inhibit HepG2.2.15 cells proliferation through inducing cellular senescence and autophagy. [BMB Reports 2019; 52(8): 520-525]

pH-Responsive Multifunctional Materials with Switchable Superamphiphobicity and Superoleophobicity-Superhydrophilicity for Controllable Oil/Water Separation

Mengnan Qu,Yichen Zhou,Lili Ma,Yi Zhang,Jiaxin Wang,Shanxin Xiong,Lihua Shen,Jinmei He 한국섬유공학회 2021 Fibers and polymers Vol.22 No.3

Stimulus-responsive materials with controllable oil/water separation performance have prodigious potentialapplication. Here, a new thought for low-cost, time-saving, flexible approach has been developed to prepare a pH-responsivematerial with switchable superamphiphobicity and superoleophobicity-superhydrophilicity. The as-prepared material can beeasily applied onto multifarious substrates and presents stable superamphiphobicity. However, when the modified material istreated by alkaline solution, its surface wettability turns superhydrophilicity and superoleophobicity, thus water is allowed topenetrate through the material whereas the oil was blocked on the surface. Moreover, the surface wettability can be recoveredto superamphiphobicity quickly via treating the material with acidic aqueous. Hence, such a controllable water wettabilityand stable oil repellency property endows the as-prepared material with excellent capability to separate water from oil/watermixture. In addition, the pH-responsive materials can maintain switchable wettability after being treated by acid and alkalinumerous cycles. Furthermore, the obtained materials also exhibit excellent recyclable, self-cleaning and flame-resistantperformance, which shows potential applications for smart water-oil separators and fire-shielding protectors.