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Cloning and expression analysis of a long type peptidoglycan recognition protein(PGRP-L) from Xenopus tropicalis 被引量:2
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作者 齐志涛 张启焕 +4 位作者 王资生 王爱民 黄贝 昌鸣先 聂品 《Zoological Research》 CAS CSCD 北大核心 2011年第4期371-378,共8页
Peptidoglycan recognition proteins(PGRPs) are a family of pattern recognition receptors(PRRs) of the immune system,which bind and hydrolyze bacterial peptidoglycan.Here,a long type PGRP(PGRP-L) was first cloned ... Peptidoglycan recognition proteins(PGRPs) are a family of pattern recognition receptors(PRRs) of the immune system,which bind and hydrolyze bacterial peptidoglycan.Here,a long type PGRP(PGRP-L) was first cloned in the lower vertebrate species Xenopus tropicalis(Xt).The XtPGRP-L possessed a conserved genomic structure with five exons and four introns.The alignment and phylogenetic analysis indicated that XtPGRP-L might be a type of amidase-like PGRP.The 3-D model showed that XtPGRP-L possessed a conserved structure compared with the Drosophila PGRP-Lb.During embryonic development,XtPGRP-L was not expressed until the 72 h tadpole stage.In adult tissues,it was strongly expressed in the liver,lung,intestine,and stomach.Furthermore,after LPS stimulation,the expression of XtPGRP-L was up-regulated significantly in the liver,intestine and spleen,indicating that XtPGRP-L may play an important role in the innate immunity of Xenopus tropicalis. 展开更多
关键词 peptidoglycan recognition protein Gene clone Expression analysis Xenopus tropicalis
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Influence of whole peptidoglycan of bifidobacterium on cytotoxic effectors produced by mouse peritoneal macrophages 被引量:15
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作者 Li Sheng Wang~1 Hui Ming Zhu~1 Dian Yuan Zhou~2 Yu Lin Wang~1 Wan Dai Zhang~2 ~1Departrnent of Gastroenterology,Shenzhen Municipal People’s Hospital,Jinan University of Medical Sciences,Shenzhen 518020,Guangdong Province,China ~2Chinese PLA Institute of Digestion,the First Military Medical University,Guangzhou 510515,Guangdong Province,ChinaLi Sheng Wang graduated and obtained Ph.D,from the First Military Medical University in 1998,now working at Department of Gastroenterology,Shenzhen Municipal People’s Hospital.Jinan University of Medical Sciences.having 35 papers published. 《World Journal of Gastroenterology》 SCIE CAS CSCD 2001年第3期440-443,共4页
INTRODUCTIONBifidobacteria are physiologically beneficial bacteria which are perdominant in human intestine ,and possess the most important functions .They play an important role in maintaining microbial balance of th... INTRODUCTIONBifidobacteria are physiologically beneficial bacteria which are perdominant in human intestine ,and possess the most important functions .They play an important role in maintaining microbial balance of the intestine .Furthermore , their presence is thought to be an important indication of health of the body [1-4].Whole peptidoglycan ( WPG) is the major component in the cell wall of bifidobacterium ,which is also a biological responsemodifier with nontoxic side dffcets. 展开更多
关键词 BIFIDOBACTERIUM Animals INTERLEUKIN-12 Interleukin-6 INTESTINES Macrophages Peritoneal MICE Mice Inbred BALB C Mice Nude Microscopy Confocal Nitric Oxide peptidoglycan Research Support Non-U.S. Gov't Tumor Necrosis Factor-alpha
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Distinct immune response induced by peptidoglycan derived from Lactobacillus sp 被引量:14
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作者 Jin Sun Yong-Hui Shi +1 位作者 Guo-Wei Le Xi-Yi Ma 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第40期6330-6337,共8页
AIM: To analyze the distinct immune responses induced by Lactobacillus peptidoglycan (PG). METHODS: BALB/c mice were intraperitoneally injected with PG once a day for three consecutive days, Peritoneal macrophage ... AIM: To analyze the distinct immune responses induced by Lactobacillus peptidoglycan (PG). METHODS: BALB/c mice were intraperitoneally injected with PG once a day for three consecutive days, Peritoneal macrophage and splenocyte mRNA was extracted and the gene expression profile was studied using high-density oligonudeotide microarrays. Inhibitory effects of Lactobacillus PG on colon tumor tissue were studied in vitro and in vivo, RESULTS: The gene expression profiles revealed that the TLR-NF-kB and Jak-STAT signaling pathways were highly activated. An inflammatory phenotype was induced when peritoneal macrophages were initially exposed to Lactobacillus PG and switched to a more complex phenotype when BALB/c mice were treated with three doses of Lactobacillus PG. A protective physiological inflammatory response was induced after three consecutive days of PG treatment. It was tending toward Thl dominant immune response. Lactobacillus PG also appeared to induce a significant in vivo anti-colon tumor effect. CONCLUSION: Lactobacillus PG is responsible for certain immune responses induced by Lactobacilli. Anti-tumor effects of Lactobacilliare likely to attribute to the activation of macrophages by PG expressed on the bacterial cell surface. 展开更多
关键词 Lactobacillus peptidoglycan Gene expression Immune response
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THE APOPTOSIS OF EXPERIMENTAL COLORECTAL CARCINOMA CELLS INDUCED BY PEPTIDOGLYCAN OF BIFIDOBACTERIUM AND THE EXPRESSION OF APOPTOTIC REGULATING GENES 被引量:5
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作者 王立生 潘令嘉 +3 位作者 施理 孙勇 张亚历 周殿元 《Chinese Journal of Cancer Research》 SCIE CAS CSCD 1999年第3期184-187,共4页
Objective: To explore the antitumor mechanisms of whole peptidoglycan of bifidobacterium. Methods: The apoptotic cells and the positive expression of bcl-2 and bax oncoprotein were studied nude mice transplantation tu... Objective: To explore the antitumor mechanisms of whole peptidoglycan of bifidobacterium. Methods: The apoptotic cells and the positive expression of bcl-2 and bax oncoprotein were studied nude mice transplantation tumors of colorectal carcinoma by employing in situ end labeling technique and immunohistochemical staining. Results: The apoptotic cell density, the positive rate and the staining intensity of bax oncoprotein of the transplantation tumor of colorectal carcinoma in the whole peptidoglycan injection group were significantly higher when compared with the tumor control group. The positive rate of bcl-2 oncoportein in the whole peptidoglycan injection group was obviously lower than that in the tumor control group (P<0.01). Conclusion: Whole peptidoglycan of Bifidobacterium bifidum could induce cell apoptosis of nude mice transplantation tumors of colorectal carcinoma by down-regulating the expression of the bcl-2 gene and upregulating the expression of the bax gene. 展开更多
关键词 BIFIDOBACTERIUM Whole peptidoglycan APOPTOSIS Colorectal carcinoma
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Chemistry and Pharmacological Activity of Peptidoglycan from Lycium Barbaruml
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作者 Zhao, CJ He, YQ +1 位作者 Li, RZ Cui, GH 《Chinese Chemical Letters》 SCIE CAS CSCD 1996年第11期1009-1010,共2页
Two homogeneous new peptidoglycans were obtained from Lycium barbarum L. Theywere found to be effective ingredients capable of resining lipid peroxidation. The componentsand linkages of the two homogeneous polysacchar... Two homogeneous new peptidoglycans were obtained from Lycium barbarum L. Theywere found to be effective ingredients capable of resining lipid peroxidation. The componentsand linkages of the two homogeneous polysaccharides were studied by means of complete acidhydrolysis, periodate oxidation. Smith degradation enzyme hydrolysis, IR, GC and aminoacid analysis. Homogeneous polysaccharide LBPC2 was found to be a β(1→4)(1→6) peptidoglycanwith MW of 1.2×104, composed of Xyl, Rha. Man in a molar ratio of8.8:2.3;1, LBPC4 was foundto be a a(1→4)(1→6) peptidoglycan with MW of 1.0×104, composed of glucans. 展开更多
关键词 ACTIVITY PHARMACOLOGICAL peptidoglycan LYCIUM Barbaruml
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Effects of different enzymatic hydrolysis methods on the bioactivity of peptidoglycan in Litopenaeus vannamei
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作者 宋晓玲 张悦 +1 位作者 韦嵩 黄倢 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2013年第2期374-383,共10页
The effects of different hydrolysis methods on peptidoglycan (PG) were assessed in terms of their impact on the innate immunity and disease resistance of Pacific white shrimp, Litopenaeus vannamei. PG derived from B... The effects of different hydrolysis methods on peptidoglycan (PG) were assessed in terms of their impact on the innate immunity and disease resistance of Pacific white shrimp, Litopenaeus vannamei. PG derived from Bifidobacteriurn thermophilum was prepared in the laboratory and processed with lysozyme and protease under varying conditions to produce several different PG preparations. A standard shrimp feed was mixed with 0.05% PG preparations to produce a number of experimental diets for shrimp. The composition, concentration, and molecular weight ranges of the soluble PG were analyzed. Serum phenoloxidase and acid phosphatase activity in the shrimp were determined on Days 6-31 of the experiment. The protective activity of the PG preparations was evaluated by exposing shrimp to white spot syndrome virus (WSSV). Data on the composition of the PG preparations indicated that preparations hydrolyzed with lysozyme for 72 h had more low-molecular-weight PG than those treated for 24 h, and hydrolysis by protease enhanced efficiency of hydrolysis compared to lysozyme. SDS-PAGE showed changes in the molecular weight of the soluble PG produced by the different hydrolysis methods. Measurements of serum phenoloxidase and acid phosphatase activity levels in the shrimp indicated that the PG preparations processed with enzymes were superior to the preparation which had not undergone hydrolysis in enhancing the activity of the two serum enzymes. In addition, the preparation containing more low-molecular-weight PG enhanced the resistance of the shrimp to WSSV, whereas no increased resistance was observed for preparations containing less low-molecular-weight PG. These findings suggest that the immunity-enhancing activity of PG is related to its molecular weight and that increasing the quantity of low-molecular-weight PG can fortify the effect of immunity enhancement. 展开更多
关键词 peptidoglycan enzymatic hydrolysis Litopenaeus vannamei PHENOLOXIDASE acid phosphatase resistance to WSSV
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Influence of whole peptidoglycan of Bifidobacterium bifidum on cytokines production by peritoneal macrophages of nude mice
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作者 王立生 潘令嘉 +3 位作者 施理 孙勇 张亚历 周殿元 《Journal of Medical Colleges of PLA(China)》 CAS 1999年第2期83-86,共4页
Objective: To explore the functions of whole peptidoglycan (WPG ) of bifidobacterium in regulating immune reactions. Methods: IL- 1 activity produced by peritoneal macrophages was investigated by murine thymocyte prol... Objective: To explore the functions of whole peptidoglycan (WPG ) of bifidobacterium in regulating immune reactions. Methods: IL- 1 activity produced by peritoneal macrophages was investigated by murine thymocyte proliferating method; The content of IL-6 and IL-12 was detected by ELISA. Results: IL--1 activity and the contents of IL--6 and IL--12 secreted by peritoneal macrophages of nude mice in the WPG injection group were significantly higher than those in the control group (P < 0. 01 ). Conclusion: WPG of bifidobacteria can activate peritoneal macrophages to secret relatively large amount of IL- 1. IL- 6 and IL- 12. 展开更多
关键词 WHOLE peptidoglycan MACROPHAGE INTERLEUKIN 1 INTERLEUKIN 6 INTERLEUKIN 12
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Identification,Phylogeny and Expressional Profiles of Peptidoglycan Recognition Protein(PGRP)Gene Family in Sinonovacula constricta
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作者 MENG Yiping LÜLiyuan +3 位作者 DAI Wenfang ZHANG Weiwei LIN Zhihua DONG Yinghui 《Journal of Ocean University of China》 SCIE CAS CSCD 2022年第4期1051-1060,共10页
Peptidoglycan recognition protein(PGRP)plays a vital role in invertebrate innate immunity system as a specific pattern recognition receptor for peptidoglycan.Bivalves possess various PGRP systems for self-defense;howe... Peptidoglycan recognition protein(PGRP)plays a vital role in invertebrate innate immunity system as a specific pattern recognition receptor for peptidoglycan.Bivalves possess various PGRP systems for self-defense;however,it has not been characterized in razor clam Sinonovacula constricta.In this study,eight PGRP coding sequences were identified and analyzed from S.constricta genome,which are designated as ScPGRP-S1,ScPGRP-S2,ScPGRP-S3,ScPGRP-S4,ScPGRP-S5,ScPGRP-S6,ScPGRP-S7,ScPGRP-S8.The results of molecular evolutionary analyses showed that all eight ScPGRP genes were highly conserved and exhi-bited a typical PGRP/amidase_2 domain as PGRP genes in other mollusks.Moreover,the presence of signal peptides was predicted in ScPGRP-S2,ScPGRP-S3 and ScPRP-S6,while a transmembrane structure only existed in ScPGRP-S6.Notably,a tertiary struc-ture analysis indicated that no disulfide bond was observed in ScPGRP-S5 and ScPGRP-S7.The mRNA transcripts analysis of ScPGRPs revealed that the high expression patterns of ScPGRP-S1 and ScPGRP-S4 were found in mantle,adductor muscle and foot,while those of ScPGRP-S2,ScPGRP-S3 and ScPGRP-S6 were observed in hepatopancreas.Furthermore,the temporal expression profiles of ScPGRPs in the hepatopancreas were analyzed by qPCR<https://www.sciencedirect.com/topics/immunology-and-microbiology/real-time-polymerase-chain-reaction>after Gram-negative Vibrio parahaemolyticus and Gram-positive Staphylococcus aureus challenges.The mRNA expressions of ScPGRP-S2,ScPGRP-S3 and ScPGRP-S6 could be induced by V.pa-rahaemolyticus and S.aureus.Overall,our findings indicated that ScPGRPs were involved in the immune defense against invaders,which constituted a comprehensive understanding of the potential role of PGRP genes in S.constricta. 展开更多
关键词 Sinonovacula constricta peptidoglycan recognition protein gene family gene expression
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The effect of nebivolol on the production of nitric oxide induced by bacterial lipopolysaccharide and peptidoglycan in mice
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作者 Fadi El-Rami Hampartsoum Barsoumian +1 位作者 Joseph Simaan Alexander M. Abdelnoor 《Natural Science》 2010年第12期1360-1368,共9页
Nitric oxide (NO) plays a pivotal role in main- taining balance of physiological events in many systems including the autonomic, cardiovas- cular, hematological, and pulmonary systems. Lipopolysaccharide (LPS) and pep... Nitric oxide (NO) plays a pivotal role in main- taining balance of physiological events in many systems including the autonomic, cardiovas- cular, hematological, and pulmonary systems. Lipopolysaccharide (LPS) and peptidoglycan (PGN), components of the outer cell membranes of Gram-negative bacteria and cell walls of Gram-positive bacteria respectively, are in- criminated in NO-induced septic shock. Ne- bivolol is a third generation β1- adrenoceptor blocker with a vasodilatory property attributed to enhanced availability of nitric oxide and re- duction of cellular oxidative stress through an unknown mechanism. The current study ex- plored the hypothesis that if nebivolol enhances the availability of NO, pretreatment with ne- bivolol may enhance production of NO in re- sponse to subsequent treatment with LPS and PGN, an observation that may have relevance in clinical septic shock. Groups of female BALB/c mice each containing 12 mice (6-8 weeks old) were injected intraperitoneally with LPS (30 μg/mouse), PGN (100 μg/mouse), nebivolol (0.25 μg/g, 0.35 μg/g, 0.7 μg/g), LPS and nebivolol (0.25 μg/g), LPS and nebivolol (0.35 μg/g), LPS and nebivolol (0.7 μg/g), PGN and nebivolol (0.25 μg/g), PGN and nebivolol (0.35μg/g). One group of mice was injected with saline and an- other served as control. Three mice from each group were bled 1, 3, 6 and 9 hours post-injec- tion, the blood was pooled and the nitrite serum levels, reflecting NO concentration, were de- termined using Greiss reagent. The following results were obtained: 1) Treatment with saline did not induce NO production;2) LPS induced NO production to a maximal limit of 545% at 9 hours as compared to treatment with saline;3) PGN did not induce NO production;4) nebivolol at most doses and periods (7 out of 10 deter- minations) increased NO production over a range of 18-110% as compared to treatment with saline;5) Nebivolol enhanced LPS-induced production of NO by 58% at a dose of 0.7 μg/gm at 9 hours. It is concluded that nebivolol in- duces NO production. At low doses nebivolol initially appeared to have a suppressive or no effect on NO production induced by LPS. In- crease in the dose of nebivolol resulted in augmentation of LPS-induced production of NO. PGN, in the dose tested, did not have an effect on NO production. 展开更多
关键词 NEBIVOLOL peptidoglycan LIPOPOLYSACCHARIDE NITRIC Oxide β1- ADRENOCEPTOR BLOCKER
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Combatting Pathogenic Bacteria with Synthetic Immunotherapeutics from Chitosan:Antibody Recruiting at Engineered Bacterial Surface with Peptidoglycan Analogs
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作者 Yuan Xu Shihao Song +2 位作者 Hongwei Duan Yinyue Deng Xue-Wei Liu 《CCS Chemistry》 CSCD 2024年第6期1448-1457,共10页
The emergence of microbial drug resistance,coupled with the paucity of new antibiotics poses an impending threat to public health.In this work,we drew inspiration from synthetic peptidoglycan oligomers and successfull... The emergence of microbial drug resistance,coupled with the paucity of new antibiotics poses an impending threat to public health.In this work,we drew inspiration from synthetic peptidoglycan oligomers and successfully constructed antibody-recruiting peptidoglycan analogs,2a-d,with excellent safety profiles and high efficiencies in recruiting antibodies across different conditions.Further,we demonstrated that these peptidoglycan analogs could be readily incorporated into bacteria cell walls,whereby both simple monoclonal and pooled human serum antibodies effectively congregated to the surfaceengineered bacteria,leading to the complete extermination of the engineered bacterial cells both in vitro and in vivo.Our peptidoglycan analog agents for recruiting endogenous antibodies to combat pathogenic bacteria enable further development of promising broad-spectrum immunotherapeutics. 展开更多
关键词 CHITOSAN bacterial infection endogenous antibodies bacterial surface engineering peptidoglycan analogs
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Antiviral function of peptidoglycan recognition protein in Spodoptera exigua(Lepidoptera:Noctuidae)
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作者 Jie Li Jie Li +7 位作者 Zhaohao Jing Qianlong Yu Guiling Zheng Bin Zhang Longsheng Xing Huan Zhang Fanghao Wan Changyou Li 《Insect Science》 SCIE CAS CSCD 2023年第4期1092-1104,共13页
Peptidoglycan recognition proteins(PGRPs)are a class of molecules that play a critical role in insect immunity.Understanding the function of PGRPs is important to improve the efficiency of microbial insecticides.In th... Peptidoglycan recognition proteins(PGRPs)are a class of molecules that play a critical role in insect immunity.Understanding the function of PGRPs is important to improve the efficiency of microbial insecticides.In this study,we investigated the role of PGRP-LB(a long type PGRP)in insect immunity against viruses using Spodoptera exigua and Spodoptera exigua multiple nucleopolyhedrovirus(SeMNPV)as an insect-virus model.We cloned and identified a PGRP-LB gene from S.exigua;the gene consisted of 7 exons that encoded a polypeptide of 234 amino acids with a signal peptide and a typical amidase domain.Expression analysis revealed that the abundance of SePGRP-LB transcripts in the fat body was greater than in other tissues.Overexpression of SePGRP-LB resulted in a significant decrease of 49%in the rate of SeMNPV-infected cells.In addition,the multiplication of SeMNPV was significantly decreased:a decrease of 79%in the production of occlusion-derived virion(ODV),and a maximum decrease of 50%in the production of budded virion(BV).In contrast,silencing of SePGRP-LB expression by RNA interference resulted in a significant 1.65-fold increase in the rate of SeMNPV-infected cells,a significant 0.54-fold increase in ODV production,a maximum 1.57-fold increase in BV production,and the larval survival dropped to 21%.Our findings show that SePGRP-LB has an antiviral function against SeMNPV,and therefore this gene may provide a target for lepidopteran pest control using virus insecticides. 展开更多
关键词 ANTIVIRAL long-type peptidoglycan recognition protein gene PGRP-LB Spodoptera exigua multiple nucleopolyhedrovirus Spodoptera exigua
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乳酸菌肽聚糖的提取纯化及其对河豚毒素的毒性消减效果研究
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作者 刘畅 王嫦娥 卢瑛 《食品与发酵工业》 CAS CSCD 北大核心 2024年第5期48-53,66,共7页
乳酸菌中提取的肽聚糖已被发现对河豚毒素具有消减作用。但肽聚糖提取工艺复杂、效率低下,阻碍了毒素消减研究。该研究以具有A3α,A1γ,A4α三种类型肽聚糖的乳酸菌为原料,通过对磷壁酸去除条件、脂质去除试剂和蛋白质的酶解工艺进行优... 乳酸菌中提取的肽聚糖已被发现对河豚毒素具有消减作用。但肽聚糖提取工艺复杂、效率低下,阻碍了毒素消减研究。该研究以具有A3α,A1γ,A4α三种类型肽聚糖的乳酸菌为原料,通过对磷壁酸去除条件、脂质去除试剂和蛋白质的酶解工艺进行优化获得高纯度肽聚糖,并采用小鼠生物法评价了纯化后的3种肽聚糖对河豚毒素(tetrodotoxin, TTX)的毒性消减效果。溶菌酶及扫描电镜结果显示,采用100 g/L三氯乙酸去除磷壁酸、50 g/L十二烷基硫酸钠溶液去除脂质、胰蛋白酶与链霉蛋白酶联用去除蛋白质后,3种肽聚糖呈现完整的球状形态,表明优化后的提取工艺对肽聚糖的球形结构完整性影响小。酶联免疫吸附法和小鼠生物法结果显示,纯化后的3种肽聚糖可以去除78%以上的TTX含量,并降低87%以上的毒性,消减效果均优于灭活菌株。由此可见,优化后的肽聚糖提取纯化工艺不会破坏肽聚糖消减TTX的主要组分,并能显著提高效率,为肽聚糖的工业化应用和毒素控制研究提供了理论基础。 展开更多
关键词 肽聚糖 乳酸菌 提取工艺 毒性消减
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Comparative analysis of peptidoglycan recognition proteins in endoparasitoid wasp Microplitis mediator 被引量:4
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作者 Rui-Juan Wang Zhe Lin +5 位作者 Hong Jiang Jiancheng Li Tusar T. Saha Ziyun Lu Zhiqiang Lu Zhen Zou 《Insect Science》 SCIE CAS CSCD 2017年第1期2-16,共15页
Peptidoglycan recognition proteins (PGRPs) are a family of innate immune receptors that specifically recognize peptidoglycans (PGNs) on the surface of a number of pathogens. Here, we have identified and characteri... Peptidoglycan recognition proteins (PGRPs) are a family of innate immune receptors that specifically recognize peptidoglycans (PGNs) on the surface of a number of pathogens. Here, we have identified and characterized six PGRPs from endoparasitoid wasp, Microplitis mediator (MmePGRPs). To understand the roles of PGRPs in parasitoid wasps, we analyzed their evolutionary relationship and orthology, expression profiles during different developmental stages, and transcriptional expression following infection with Gram-positive and -negative bacteria and a fungus. MmePGRP-S1 was significantly induced in response to pathogenic infection. This prompted us to evaluate the effects of RNA interference mediated gene specific knockdown ofMmePGRP-S1. The knockdown of MmePGRP-S1 (iMmePGRP-S1) dramatically affected wasps' survival following challenge by Micrococcus luteus, indicating the involvement of this particular PGRP in immune responses against Gram-positive bacteria. This action is likely to be mediated by the Toll pathway, but the mechanism remains to be determined. MmePGRP-S 1 does not play a significant role in anti-fungal immunity as indicated by the survival rate of iMmePGRP-S wasps. This study provides a comprehensive characterization of PGRPs in the economically important hymenopteran species M. mediator. 展开更多
关键词 endoparasitoid wasp insect immunity microbial infection Microplitis mediator peptidoglycan recognition protein
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乳酸菌肽聚糖对雏鸭饲粮中黄曲霉毒素B 1的脱毒效果研究
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作者 邵怡豪 王煜琦 +3 位作者 张宇豪 张广明 肖发沂 李庆梅 《动物营养学报》 CAS CSCD 北大核心 2024年第7期4339-4349,共11页
本试验旨在探究乳酸菌肽聚糖对黄曲霉毒素B_(1)(AFB_(1))的吸附作用,为乳酸菌肽聚糖的制备和饲粮中AFB_(1)的脱毒提供科学依据及理论基础。试验以4种乳酸菌(嗜酸乳杆菌、嗜热链球菌、罗伊氏乳杆菌和植物乳杆菌)为原料提取乳酸菌肽聚糖,... 本试验旨在探究乳酸菌肽聚糖对黄曲霉毒素B_(1)(AFB_(1))的吸附作用,为乳酸菌肽聚糖的制备和饲粮中AFB_(1)的脱毒提供科学依据及理论基础。试验以4种乳酸菌(嗜酸乳杆菌、嗜热链球菌、罗伊氏乳杆菌和植物乳杆菌)为原料提取乳酸菌肽聚糖,采用高效液相色谱法比较4种乳酸菌肽聚糖对AFB_(1)的体外吸附率,选取体外吸附效果最好的罗伊氏乳杆菌肽聚糖进行动物试验。选择1日龄健康樱桃谷鸭120只,随机分为5组,每组4个重复,每个重复6只。对照组饲喂基础饲粮,AFB_(1)组在基础饲粮中添加0.10 mg/kg AFB_(1),试验组在AFB_(1)组饲粮中分别添加0.10%(Ⅰ组)、0.15%(Ⅱ组)和0.20%(Ⅲ组)罗伊氏乳杆菌肽聚糖。预试期3 d,正试期21 d。结果表明:1)乳酸菌肽聚糖种类、添加量及二者的交互作用均能够显著影响AFB_(1)的体外吸附率(P<0.05),其中10.0 mg/mL罗伊氏乳杆菌肽聚糖对AFB_(1)的体外吸附率最高,达75.29%。2)与对照组相比,AFB_(1)组的平均日增重、平均日采食量显著降低(P<0.05),料重比显著升高(P<0.05);血浆谷草转氨酶(AST)、谷丙转氨酶(ALT)、碱性磷酸酶(AKP)活性及丙二醛(MDA)含量显著升高(P<0.05),肝脏、脾脏、胸腺和法氏囊指数显著升高(P<0.05),血浆免疫球蛋白G(IgG)、免疫球蛋白M(IgM)、γ-干扰素(IFN-γ)、白细胞介素-2(IL-2)、白细胞介素-4(IL-4)含量和超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)活性及总抗氧化能力(T-AOC)显著降低(P<0.05)。3)与AFB_(1)组相比,Ⅰ、Ⅱ、Ⅲ组的平均日增重显著升高(P<0.05),料重比显著降低(P<0.05);Ⅰ、Ⅱ、Ⅲ组的血浆IgG、IFN-γ、IL-2、IL-4含量和SOD、GSH-Px活性显著升高(P<0.05),血浆AST、AKP、ALT活性及MDA含量显著降低(P<0.05);Ⅱ、Ⅲ组的胸腺和法氏囊指数显著降低(P<0.05)。由此可见,不同乳酸菌肽聚糖对AFB_(1)体外吸附效果不同,饲粮中添加罗伊氏乳杆菌肽聚糖能够部分消除AFB_(1)对雏鸭造成的生长性能下降,改善AFB_(1)所导致的免疫功能降低以及肝脏毒性。 展开更多
关键词 肽聚糖 乳酸菌 黄曲霉毒素B 1 生长性能 脱毒效果
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强直性脊柱炎患者血清PGLYRP-1、PTX3水平及其与炎症水平、骨密度的相关性
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作者 田洪波 汲会静 胡敬暖 《检验医学与临床》 CAS 2024年第20期3063-3067,共5页
目的探讨血清肽聚糖识别蛋白1(PGLYRP-1)、正五聚蛋白3(PTX3)水平及其与强直性脊柱炎(AS)患者炎症水平、骨密度(BMD)的相关性。方法选取2021年1月至2023年1月该院收治的68例AS患者作为AS组,另选取同期健康体检者68例作为非AS组。检测所... 目的探讨血清肽聚糖识别蛋白1(PGLYRP-1)、正五聚蛋白3(PTX3)水平及其与强直性脊柱炎(AS)患者炎症水平、骨密度(BMD)的相关性。方法选取2021年1月至2023年1月该院收治的68例AS患者作为AS组,另选取同期健康体检者68例作为非AS组。检测所有研究对象血清PGLYRP-1、PTX3水平。采用Pearson相关分析AS患者血清PGLYRP-1、PTX3水平与炎症相关因子水平及不同部位处BMD的相关性。采用多因素Logistic回归分析PGLYRP-1、PTX3对AS发生的影响。结果AS组与非AS组工作状况、身高、身体质量指数、体质量、婚姻状况比较,差异均无统计学意义(P>0.05)。AS组红细胞沉降率、巴氏强直性脊柱炎疾病活动性指数评分、巴氏强直性脊柱炎功能指数评分均明显高于非AS组,差异均有统计学意义(P<0.05)。AS组PGLYRP-1、PTX3水平均高于非AS组,差异均有统计学意义(P<0.05)。AS组IL-1β、IL-6、IL-17、IL-18、TNF-α、CRP水平均高于非AS组,差异均有统计学意义(P<0.05)。AS组腰椎、股骨颈、华氏三角、股骨粗隆处的BMD显著低于非AS组(P<0.05)。AS患者血清PGLYRP-1、PTX3水平与IL-1β、IL-6、IL-17、IL-18、TNF-α、CRP水平均呈正相关(P<0.05)。AS患者血清PGLYRP-1、PTX3水平与腰椎、股骨颈、华氏三角、股骨粗隆处BMD均呈负相关(P<0.05)。多因素Logistic回归分析结果显示,PGLYRP-1、PTX3水平升高均是AS发生的独立危险因素(P<0.05)。结论AS患者血清PGLYRP-1、PTX3表达水平较高,与炎症因子水平的上升有关,且与患者不同部位BMD呈负相关,可能成为AS病情监测的有效标志物。 展开更多
关键词 强直性脊柱炎 肽聚糖识别蛋白1 正五聚蛋白3 炎症水平 骨密度 相关性
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用于标记细菌肽聚糖的荧光D-氨基酸的研究进展
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作者 李龙辉 涂其冬 《山东化工》 CAS 2024年第9期92-97,共6页
肽聚糖(Peptidoglycan,PG)是细菌细胞壁的主要组成成分,对于维持细胞形态、稳定胞体渗透压起重要作用,干扰PG的生物合成会破坏细胞壁结构,导致细菌死亡。细菌中普遍存在L-和D-氨基酸,其中D-氨基酸是PG合成的基本单元。荧光D-氨基酸(Fluo... 肽聚糖(Peptidoglycan,PG)是细菌细胞壁的主要组成成分,对于维持细胞形态、稳定胞体渗透压起重要作用,干扰PG的生物合成会破坏细胞壁结构,导致细菌死亡。细菌中普遍存在L-和D-氨基酸,其中D-氨基酸是PG合成的基本单元。荧光D-氨基酸(Fluorescent D-amino acids,FDAAs)是修饰有荧光基团的D-氨基酸类似物,可被细菌内源性转肽酶识别并整合在PG层中,所携带的荧光基团能够在新合成的PG上释放荧光信号。哺乳动物细胞通常无法识别D-氨基酸,因此,这种荧光标记策略能够在生物体内应用。近年来,FDAAs已成为可视化细菌PG生长和重塑的强大工具。本文围绕目前已开发的FDAAs展开讨论,并介绍这种标记策略在可视化PG增长、细菌抗生素敏感性分析、肠道菌群研究以及细菌感染治疗等的应用,最后对该研究方向的发展前景进行了展望。 展开更多
关键词 肽聚糖 细胞壁 荧光 D-氨基酸
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皱纹盘鲍肽聚糖识别蛋白的表达及免疫功能特性
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作者 乔琨 郑春花 +5 位作者 陈贝 苏永昌 郝华 许旻 蔡水淋 刘智禹 《大连海洋大学学报》 CAS CSCD 北大核心 2023年第6期947-955,共9页
为研究皱纹盘鲍(Haliotis discus hannai)肽聚糖识别蛋白HdhPGRP-SC2-like的免疫功能特性,利用RACE技术克隆了HdhPGRP-SC2-like基因的全长cDNA序列,采用实时荧光定量PCR(qPCR)分析了HdhPGRP-SC2-like基因的组织分布特征,通过原核表达获... 为研究皱纹盘鲍(Haliotis discus hannai)肽聚糖识别蛋白HdhPGRP-SC2-like的免疫功能特性,利用RACE技术克隆了HdhPGRP-SC2-like基因的全长cDNA序列,采用实时荧光定量PCR(qPCR)分析了HdhPGRP-SC2-like基因的组织分布特征,通过原核表达获得了重组蛋白rHdhPGRP-SC2-like,并对其酰胺酶活性及免疫特性进行了验证。结果表明:HdhPGRP-SC2-like基因的cDNA全长为938 bp,开放阅读框为780 bp,编码260个氨基酸,包含保守的PGRP结构域和Ami_2结构域;HdhPGRP-SC2-like属于短型PGRP,与软体动物近缘物种PGRP具有高度相似性;qPCR分析显示,HdhPGRP-SC2-like mRNA在皱纹盘鲍各组织中均有表达,其中,鳃中表达量最高,外套膜、消化腺中表达量次之,腹足和血细胞中表达量较低;进一步构建原核表达载体pET-28a(+)-HdhPGRP-SC2-like,经诱导表达、分离纯化获得重组蛋白rHdhPGRP-SC2-like,该蛋白具有肽聚糖结合活性,且在Zn2+存在的情况下显示出酰胺酶活性。研究表明,HdhPGRP-SC2-like能够结合细菌肽聚糖成分,在机体抵御入侵细菌等免疫防御中发挥重要作用。 展开更多
关键词 皱纹盘鲍 肽聚糖识别蛋白 酰胺酶活性 免疫防御 细菌结合
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高表达GFP-PBP1b融合蛋白的猪链球菌菌株的构建及PBP1b蛋白细胞定位的研究 被引量:1
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作者 武柳君 卫东 +3 位作者 高广娟 陈平 刘思国 张跃灵 《中国预防兽医学报》 CAS CSCD 北大核心 2023年第11期1101-1107,共7页
为鉴定猪链球菌(Streptococcus suis)A型青霉素结合蛋白PBP1b在S.suis中的细胞定位,本研究经PCR扩增S.suis pbp1b基因融合位点上下游序列UP和DN、强启动子Peno基因片段及绿色荧光蛋白(GFP)gfp基因片段,再通过重叠延伸PCR扩增构建融合片... 为鉴定猪链球菌(Streptococcus suis)A型青霉素结合蛋白PBP1b在S.suis中的细胞定位,本研究经PCR扩增S.suis pbp1b基因融合位点上下游序列UP和DN、强启动子Peno基因片段及绿色荧光蛋白(GFP)gfp基因片段,再通过重叠延伸PCR扩增构建融合片段UP-Peno-GFP-DN。利用同源重组的方法将UP-Peno-GFP-DN转化含反向筛选标记的PSS-pbp1b中间菌株,经含7%蔗糖的TSAS平板筛选,挑单菌落进行PCR及测序鉴定。PCR及测序鉴定结果显示,获得的重组菌株中Peno-gfp片段替换了PSS-pbp1b中的PSS片段,表明融合强启动子Peno、GFP及PBP1b(GFP-PBP1b)的重组菌株P-GFP-pbp1b正确构建。以S.suis 05ZYH33株和本实验室前期构建的GFP-pbp1b为对照,培养P-GFP-pbp1b菌株并测定OD600nm值,绘制各菌株的生长曲线;采用western blot检测P-GFP-pbp1b菌株中GFP-PBP1b融合蛋白的表达水平,并与GFP-pbp1b菌株进行比较;利用Alexa Fluor 633-WGA染色,经超高分辨显微镜观察GFP-pbp1b和P-GFP-pbp1b菌株形态及GFP-PBP1b融合蛋白在S.suis细胞中的定位。生长曲线结果显示,S.suis融合菌株GFP-pbp1b和P-GFP-pbp1b均正常生长;western blot结果显示,GFP-pbp1b和P-GFP-pbp1b菌株均能够表达GFP-PBP1b融合蛋白,但强启动子驱动的P-GFP-pbp1b菌株中GFP-PBP1b蛋白表达量较GFP-pbp1b菌株提高了6倍(P<0.01);超高分辨显微镜观察结果显示,GFP-pbp1b和P-GFP-pbp1b菌株形态均正常,GFP-pbp1b菌株中GFP荧光较弱,难以定位GFP-PBP1b,而P-GFP-pbp1b菌株中GFP荧光较强,能够明显观察到融合蛋白GFP-PBP1b定位在S.suis的细胞横隔和两极。本研究通过构建高表达GFP-PBP1b融合蛋白的P-GFP-pbp1b菌株首次观察到PBP1b在S.suis中的细胞定位,为进一步研究PBP1b在S.suis细胞壁肽聚糖合成中的作用奠定了基础。 展开更多
关键词 猪链球菌 荧光蛋白融合菌株 A型青霉素结合蛋白 PBP1b 细胞壁肽聚糖合成
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枯草芽孢杆菌肽聚糖对绵羊瘤胃上皮细胞β-防御素-1(SBD-1)表达的影响 被引量:1
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作者 齐盟 辛雅明 +2 位作者 白绥明 胡亮 杨银凤 《中国兽医杂志》 CAS 北大核心 2023年第11期52-58,共7页
为了探究来源于枯草芽孢杆菌细胞壁的肽聚糖对绵羊瘤胃上皮细胞(ORECs)中β-防御素-1(SBD-1)表达的影响,本试验使用30μg/mL肽聚糖刺激ORECs不同时间(2、4、6、8、10和12 h),采用荧光定量PCR(qPCR)和酶联免疫吸附试验(ELISA)方法分别检... 为了探究来源于枯草芽孢杆菌细胞壁的肽聚糖对绵羊瘤胃上皮细胞(ORECs)中β-防御素-1(SBD-1)表达的影响,本试验使用30μg/mL肽聚糖刺激ORECs不同时间(2、4、6、8、10和12 h),采用荧光定量PCR(qPCR)和酶联免疫吸附试验(ELISA)方法分别检测SBD-1的mRNA和蛋白表达量,确定最佳刺激时间;再使用不同浓度的肽聚糖(0、10、20、30、40和50μg/mL)刺激ORECs 2 h,采用qPCR和ELISA方法检测SBD-1的mRNA和蛋白表达量,确定最佳刺激浓度。结果显示:(1)使用30μg/mL肽聚糖刺激ORECs不同时间时,SBD-1的mRNA和蛋白表达量随着时间的增加呈先下降后升高的趋势,2 h时表达量最多并极显著高于对照组(P<0.001)。(2)使用不同浓度肽聚糖刺激ORECs 2 h时,SBD-1的mRNA和蛋白表达量随着肽聚糖浓度的升高呈现先升高后降低的趋势,在20μg/mL时表达量最多并极显著高于对照组(P<0.001)。(3)不同时间刺激试验和不同浓度刺激试验均不会对ORECs产生细胞毒性作用。结果表明,来源于枯草芽孢杆菌的肽聚糖能够诱导ORECs表达SBD-1,最佳刺激条件为20μg/mL枯草芽孢杆菌肽聚糖刺激ORECs 2 h。 展开更多
关键词 枯草芽孢杆菌肽聚糖 绵羊瘤胃上皮细胞(ORECs) β-防御素-1(SBD-1) 荧光定量PCR(qPCR) 酶联免疫吸附试验(ELISA) CCK8
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硒化枯草芽孢杆菌肽聚糖的结构表征及体外抗氧化活性研究
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作者 杨智翔 殷海成 王金荣 《河南工业大学学报(自然科学版)》 CAS 北大核心 2023年第4期84-91,共8页
为探究硒化肽聚糖(Se-PG)的结构与抗氧化能力,以枯草芽孢杆菌(Bacillus subtilis)胞壁肽聚糖(PG)和亚硒酸钠为原料,利用HNO_(3)-Na_(2)SeO_(3)法对PG进行硒化修饰,制备Se-PG复合物。通过紫外光谱、傅里叶红外光谱及核磁共振研究Se-PG结... 为探究硒化肽聚糖(Se-PG)的结构与抗氧化能力,以枯草芽孢杆菌(Bacillus subtilis)胞壁肽聚糖(PG)和亚硒酸钠为原料,利用HNO_(3)-Na_(2)SeO_(3)法对PG进行硒化修饰,制备Se-PG复合物。通过紫外光谱、傅里叶红外光谱及核磁共振研究Se-PG结构特征,从对DPPH、ABTS、·OH自由基的清除能力评价其体外抗氧化活性。结果表明:Se-PG的硒含量为369.32μg/g,傅里叶红外光谱在890 cm_(-1)有吸收峰,表明形成亚硒酸酯键;Se-PG对DPPH、ABTS和·OH自由基清除率具有质量浓度依赖效应,当质量浓度达到5 mg/mL时,自由基清除率分别为39.51%±0.26%、39.47%±0.98%、48.38%±1.42%,显著高于亚硒酸钠和PG(P<0.05)。结构表征表明B.subtilis PG可进行硒化修饰且不改变PG的基本结构。Se-PG具有优越的体外自由基清除能力和抗氧化活性,可作为功能性抗氧化剂进行开发。 展开更多
关键词 硒化修饰 枯草芽孢杆菌肽聚糖 结构表征 抗氧化活性
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