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Relevant bibliographies by topics / Lb-Protease

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Academic literature on the topic 'Lb-Protease'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Lb-Protease"

1

Swaroop, Sarkar, V.V.S.Suryanarayana, and Shankar S.R.Madhan. "CLONING AND EXPRESSION OF LB-PROTEASE FROM CDNA CLONE OF FOOT-AND- MOUTH DISEASE VIRUS." International Journal of Research - Granthaalayah 5, no. 9SE (2017): 62–71. https://doi.org/10.5281/zenodo.1020885.

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Foot-and –Mouth disease virus (FMDV) is a positive sense RNA virus and the genome codes for single polyprotein. The FMDV L protein is located at the N terminus of the polyprotein and is the first gene product released from the nascent polyprotein. The leader L protease which is involved in pathogenesis has two known functions: (i) auto-catalytic removal from the N terminus of the viral polyprotein and (ii) cleavage of the p220 subunit of the eukaryotic initiation factor 4F complex, which helps to shut off host protein synthesis. To explore the role of L protease in FMDV pathogenesis we generat

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2

Goo, Eunhye, and Ingyu Hwang. "Essential roles of Lon protease in the morpho-physiological traits of the rice pathogen Burkholderia glumae." PLOS ONE 16, no. 9 (2021): e0257257. http://dx.doi.org/10.1371/journal.pone.0257257.

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The highly conserved ATP-dependent Lon protease plays important roles in diverse biological processes. The lon gene is usually nonessential for viability; however, lon mutants of several bacterial species, although viable, exhibit cellular defects. Here, we show that a lack of Lon protease causes pleiotropic effects in the rice pathogen Burkholderia glumae. The null mutation of lon produced three colony types, big (BLONB), normal (BLONN), and small (BLONS), in Luria–Bertani (LB) medium. Colonies of the BLONB and BLONN types were re-segregated upon subculture, while those of the BLONS type were

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3

Grujović, Mirjana, Katarina Mladenović, Violeta Jakovljević, and Ljiljana Čomić. "Detection of enzymes produced by lactic acid bacteria isolated from traditionally made Serbian cheese and their role in the formation of its specific flavor." Acta agriculturae Serbica 25, no. 50 (2020): 165–69. http://dx.doi.org/10.5937/aaser2050165g.

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Nine species (sixteen isolates) of lactic acid bacteria (LAB) isolated from traditionally made Serbian cheese were evaluated for their enzymatic activities in order to select indigenous strains of technical interest for the manufacture of cheese. These strains were selected based on their previously determined biochemical and physiological characteristics, as well as their antimicrobial activity, and were identified as Lactococcus lactis subsp. lactis (one isolate), Lc. lactis subsp. lactis biovar. diacetylactis (five isolates), Lactobacillus fermentum (two isolates), Lb. plantarum (one isolat

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4

Alifiya, Q., E. Taufik, M. S. Soenarno, M. Arifin, and C. Budiman. "Utilization of whey-based growth media for production of recombinant papain-like protease of SARS- CoV-2 under Escherichia coli host cells." IOP Conference Series: Earth and Environmental Science 1359, no. 1 (2024): 012014. http://dx.doi.org/10.1088/1755-1315/1359/1/012014.

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Abstract The Papain-like protease (Plpro) of the SARS-CoV-2 virus represents a potential therapeutic target for combating Coronavirus Disease 2019 (COVID-19). Due to its practicality and cost-effectiveness, recombinant production of Plpro is conventionally achieved through Escherichia coli. However, this process’s synthetic Luria-Bertani (LB) medium remains economically burdensome. This study explores the feasibility of substituting LB medium with whey, a by-product of cheese processing renowned for its rich nutritional profile. Employing whey as an alternative growth medium for E. coli, the s

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5

ACHMAD, DWI ISYANA, IHSANAWATI, and RUKMAN HERTADI. "ISOLATION AND CHARACTERIZATION OF A SURFACTANT-STABLE PROTEASE FROM HALOPHILIC BACTERIA Chromohalobacter Japonicus BK-AB18." Malaysian Applied Biology 49, no. 2 (2021): 37–42. http://dx.doi.org/10.55230/mabjournal.v49i2.1520.

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The protease from Chromohalobacter japonicus BK-AB18 was produced by growing bacteria in a LB medium containing 5% casein and 5% NaCl. The crude protease was partially purified by three levels of ammonium sulfate concentration (ranges of 0–70%, 70–75% and 75–80%) and the highest specific activity was exhibited in the range of 75–80%. The enzyme has a relative molecular weight of 65 kDa. The protease in this fraction had the highest activity in the following optimum conditions: 7.5% NaCl, a pH of 9.0 and a temperature of 45°C. The activity of the enzyme at the optimum pH and temperature was enh

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6

Ramlucken, Uraisha, Krishna Suresh Babu Naidu, and Patrick Govender. "Improved Production of HIV-1 Subtype C Protease from Transgenic E. Coli." Open Microbiology Journal 15, no. 1 (2021): 168–76. http://dx.doi.org/10.2174/1874285802115010168.

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Background: Human Immunodeficiency Virus 1 (HIV-1) subtype C is responsible for the majority of infections of patients in Southern Africa. The HIV protease is a primary target for the development of highly efficient anti-retroviral pharmaceuticals because of its pivotal role in the maturation of the virus in the host cell. For target validation of novel HIV protease inhibitors, there is a need for the availability of an abundance of this protease. Objective: This study reports an optimized method to produce HIV-1 protease derived from HIV-1 subtype C. Methods: It involves the use of a transgen

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7

Sarkar, Swaroop, V. V. S. Suryanarayana, and S. R. Madhan Shankar. "CLONING AND EXPRESSION OF Lb-PROTEASE FROM cDNA CLONE OF FOOT-AND- MOUTH DISEASE VIRUS." International Journal of Research -GRANTHAALAYAH 5, no. 9(SE) (2017): 62–71. http://dx.doi.org/10.29121/granthaalayah.v5.i9(se).2017.2258.

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Foot-and –Mouth disease virus (FMDV) is a positive sense RNA virus and the genome codes for single polyprotein. The FMDV L protein is located at the N terminus of the polyprotein and is the first gene product released from the nascent polyprotein. The leader L protease which is involved in pathogenesis has two known functions: (i) auto-catalytic removal from the N terminus of the viral polyprotein and (ii) cleavage of the p220 subunit of the eukaryotic initiation factor 4F complex, which helps to shut off host protein synthesis. To explore the role of L protease in FMDV pathogenesis we generat

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8

Aihara, Morio, Ken Tamura, Ryuko Kawarada, Keizou Okawa, and Yutaka Yoshida. "Glycoprotein Ib Has a Partial Role in Platelet-von Willebrand Factor Collagen Interaction." Thrombosis and Haemostasis 60, no. 02 (1988): 182–87. http://dx.doi.org/10.1055/s-0038-1647026.

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SummaryThe adhesion of human fixed washed platelets (FWP) to collagen was decreased after treatment with Serratia marcescens protease (SP), which removed 95% of the glycocalicin from platelet membrane glycoprotein (GP) lb. However, the diminished adhesion of SP treated FWP to collagen could still be increased in the presence of purified von Willebrand factor (vWF). This ability of vWF to increase FWP adhesion to collagen is defined as collagen cofactor (CCo). The adhesion of FWP to collagen was not affected by a monoclonal antibody (MAb) to GP Ilb/IIIa (10E5), that inhibits ADP and collagen in

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9

Saima Bibi, Haroon Ibrahiam, and Arzoo Nazir. "Detection of Proteases from Bacillus Species Isolated from Agricultural Soil." Indus Journal of Bioscience Research 3, no. 3 (2025): 108–14. https://doi.org/10.70749/ijbr.v3i3.774.

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Present research project was conducted to investigate the protease production by gram positive Bacillus species and to investigate their role in dehairing of animal hides. Proteases are widely employed as they have replaced the use of conventional chemical based dehairing methods as they are ecofriendly, easy to cultivate and have high productivity rate. Experimental work was conducted in September, 2022 to July, 2023. 25 agricultural soil samples were collected from different local areas of Haripur and subjected to isolation and purification of Bacillus strains using LB media. Out of 25 sampl

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10

McInerney, Gerald M., Andrew M. Q. King, Natalie Ross-Smith, and Graham J. Belsham. "Replication-competent foot-and-mouth disease virus RNAs lacking capsid coding sequences." Microbiology 81, no. 7 (2000): 1699–702. http://dx.doi.org/10.1099/0022-1317-81-7-1699.

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RNA transcripts were prepared from plasmids encoding an infectious cDNA of foot-and-mouth disease virus (FMDV) or derivatives in which the leader (Lab and Lb) and capsid protein coding sequences were deleted or replaced by sequences encoding chloramphenicol acetyltransferase (CAT). The transcripts were electroporated into BHK cells and the expression of CAT and the FMDV 3C protease was monitored. Detection of CAT and 3C was dependent on the ability of the transcript to replicate. All of the Lb coding sequence and 94% of P1 (the capsid protein precursor) coding sequence could be deleted without

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Conference papers on the topic "Lb-Protease"

1

Sun, Xiao-Xin, Xia He, Li Yin, Rosalie Sears, and Mushui Dai. "Abstract LB-074: The nucleolar ubiquitin-specific protease USP36 deubiquitinates and stabilizes c-Myc." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-lb-074.

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Meyer, M., I. Schellenberg, B. Hofmann, and G. Vogel. "A GENETIC VARIANT OP PLATELET MEMBRANE GLYCOPROTEIN lb ASSOCIATED WITH A MILD BLEEDING DISORDER." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643510.

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Mild bleeding symptoms in a female patient were shown to be related to defective platelet function: Aggregation induced by ADP and PAP was decreased and platelet spreading was disturbed. Platelet membrane glycoproteins were analyzed by various electrophoretic procedures (SDS electrophoresis, nonreduced-reduced 2-dimensional and high resolution 2-dimensional electrophoresis). These studies revealed a decreased concentration of normal glycoprotein lb (GP Ib) and the appearance of an additional glycopeptide with an apparent Mr of 160.000 under reducing conditions. This component was strongly labe

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Pant, Shishir Mani, Topi Tervonen, Denis Belitskin, et al. "Abstract LB-204: Oncogenic Ras signaling requires serine protease hepsin to induce invasive breast cancer phenotype." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-lb-204.

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4

Aakhus, A. M., N. O. Solum, and I. Hagen. "EFFECTS OF SOME ORGANIC SOLVENTS ON GP lb AND ACTIN-BINDING PROTEIN IN BLOOD PLATELETS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643511.

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Effects on filamentous proteins appear to be a central phenomenon in the neuronal toxic effects of organic solvents. We have therefore compared the effects of some organic solvents (particularly isopropylalcohol, IPA) to the previously observed effects of dibucaine (DBC) on platelet cytoskeletal proteins. Incubation of platelets with 6% IPA at 37° C, like DBC, initiates a degradation of actin-binding protein (ABP) as substrate for a calcium activated protease (CAP), shown by SDS-PAGE. IPA leads to an increase followed by a decrease in bovine von Willebrand factor-induced agglutination. The dec

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5

Godeau, François, Patricia Leneuve, Laetitia D. Costa, Yves L. Bouc, and Jack-Michel Renoir. "Abstract LB-238: Antitumor activity of mini-IGFBP-3, a protease-resistant derivative of human IGF binding protein-3." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-lb-238.

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Gocheva, Vasilena, Hao-Wei Wang, Bedrick Gadea, et al. "Abstract LB-379: IL-4 induces cathepsin protease activity in tumor-associated macrophages to promote cancer growth and invasion." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-lb-379.

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7

Sas, G. "DEFECTS IN SERINE PROTEASE INHIBITORS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643714.

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Several serine protease inhibitorsof plasma inhibit the activated coagulation enzymes but only antithrombin III(AT-III)and heparin cofactor II (HC-II) are implicated in the pathogenesisof the familial thrombosis. Since thefirst publication (1965) many thrombophilic families with reduced AT-III synthesis have been investigated. These studies have proved that the disorder is associated with a high risk forvenous thrombosis and the inheritanceis autosomal dominant. The AT-III activity in the plasma of the affected patients is about 50% of the normalvalue.In recent years the heterogeneity of the i

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Oh, Eunhye, Daeil Sung, Yoon-Jae Kim, et al. "Abstract LB-311: Inhibition of ubiquitin-specific protease 34 (USP34) regenerates mammary glands via induction of epithelial-mesenchymal transition (EMT) and stemness." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-lb-311.

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9

Pareti, F. I., K. Nliya, P. J. Kostel, J. M. McPherson, T. S. Zimmerman, and Z. M. Ruggeri. "IDENTIFICATION OF A SECOND COLLAGEN-BINDING DOMAIN IN HUMAN VON WILLEBRAND FACTOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642877.

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We have recently reported (Journal of Biological Chemistry 261: 15310-15315, 1986) that von Willebrand factor (vWF) possesses a collagen-binding domain localized in a reduced and alkylated tryptic fragment of apparent 52/48 kDa molecular weight extending between residues Val (449) and Lys (728) of the constituent subunit. This proteolytic fragment of vWF also contains a glycoprotein lb-binding domain and a heparin-binding domain. We have now identified a second collagen-binding domain in the Staphylococcus aureus V8 protease-generated fragment I that extends from residue Gly (911) to Glu (1365

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10

Wyler, B., and K. J. Clemetson. "THE ROLE OF GPIb IN PLATELET ACTIVATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642922.

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Platelet membrane glycoprotein lb (GPIb) is known to contain a receptor for von Willebrand factor (vWf) and for thrombin. The role of GPIb in platelet activation was investigated by comparing the effect of removal of the binding sites by specific proteolysis with that of blocking them using specific antibodies. Specific removal of the 45 kDa outer part of GPIb by treatment of platelets with human leukocyte elastase caused loss of platelet agglutination response to von Willebrand factor (vWf) but also a weaker activation by thrombin similar to that found with Bernard-Soulier syndrome platelets

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