On the public citation graph
Characterization of Bacillus subtilis -glutamyltransferase and its involvement in the degradation of capsule poly- -glutamate
0 signed · 152 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/bbrc.1999.1298openalex-snapshot
A Poly-γ-glutamate Synthetic System of Bacillus subtilis IFO 3336: Gene Cloning and Biochemical Analysis of Poly-γ-glutamate Produced by Escherichia coli Clone Cells
inferredcites →https://doi.org/10.1007/bf00232585openalex-snapshot
γ-Glutamyl transpeptidase: catalytic, structural and functional aspects
inferredcites →https://doi.org/10.1007/s00018-002-8431-9openalex-snapshot
Bacillus subtilis sporulation and stationary phase gene expression
inferredcites →https://doi.org/10.1016/0076-6879(80)66525-2openalex-snapshot
[95] Folylpolyglutamate endopeptidase from chicken intestine: Isolation with the aid of affinity chromatography
inferredcites →https://doi.org/10.1016/0076-6879(87)53044-0openalex-snapshot
[1] Production of single-stranded plasmid DNA
inferredcites →https://doi.org/10.1016/0141-8130(94)90032-9openalex-snapshot
γ-Poly(glutamic acid) formation by Bacillus licheniformis 9945a: physiological and biochemical studies
inferredcites →https://doi.org/10.1016/0378-1119(95)00652-4openalex-snapshot
Antibiotic-resistance cassettes for Bacillus subtilis
inferredcites →https://doi.org/10.1016/s0021-9258(20)82150-4openalex-snapshot
Isolation and characterization of pteroylpolyglutamate hydrolase from rat intestinal mucosa.
inferredcites →https://doi.org/10.1016/s0076-6879(85)13053-3openalex-snapshot
[50] γ-Glutamyl transpeptidase from kidney
inferredcites →https://doi.org/10.1016/s0141-0229(02)00314-9openalex-snapshot
Salt-tolerant γ-glutamyltranspeptidase from Bacillus subtilis 168 with glutaminase activity
inferredcites →https://doi.org/10.1016/s0168-6445(98)00003-5openalex-snapshot
Rolling-circle plasmids from Bacillus subtilis: complete nucleotide sequences and analyses of genes of pTA1015, pTA1040, pTA1050 and pTA1060, and comparisons with related plasmids from Gram-positive bacteria
inferredcites →https://doi.org/10.1016/s0378-1119(96)00404-0openalex-snapshot
Plasmids for ectopic integration in Bacillus subtilis
inferredcites →https://doi.org/10.1021/bi00075a026openalex-snapshot
Extracellular glutathione is a source of cysteine for cells that express .gamma.-glutamyl transpeptidase
inferredcites →https://doi.org/10.1038/36786openalex-snapshot
The complete genome sequence of the Gram-positive bacterium Bacillus subtilis
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.02069.xopenalex-snapshot
Divergent structure of the ComQXPA quorum‐sensing components: molecular basis of strain‐specific communication mechanism in Bacillus subtilis
inferredcites →https://doi.org/10.1073/pnas.93.15.7923openalex-snapshot
Growth retardation and cysteine deficiency in gamma-glutamyl transpeptidase-deficient mice.
inferredcites →https://doi.org/10.1074/jbc.m008484200openalex-snapshot
Expression of γ-Glutamyl Transpeptidase Protects Ramos B Cells from Oxidation-induced Cell Death
inferredcites →https://doi.org/10.1086/341299openalex-snapshot
Effect of the Lower Molecular Capsule Released from the Cell Surface of Bacillus anthracis on the Pathogenesis of Anthrax
inferredcites →https://doi.org/10.1093/nar/23.16.3214openalex-snapshot
Characterization of the replication region of the acillus subtilis plasmid pLS20: a noval type to replicon
inferredcites →https://doi.org/10.1096/fasebj.13.1.69openalex-snapshot
Hydrogen peroxide produced during γ‐glutamyl transpeptidase activity is involved in prevention of apoptosis and maintainance of proliferation in U937 cells
inferredcites →https://doi.org/10.1099/00221287-143-6-1885openalex-snapshot
An important role for glutathione and γ-glutamyltranspeptidase in the supply of growth requirements during nitrogen starvation of the yeast Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1099/mic.0.27045-0openalex-snapshot
Roles and regulation of the glutamate racemase isogenes, racE and yrpC, in Bacillus subtilis
inferredcites →https://doi.org/10.1111/j.1365-2958.1988.tb00041.xopenalex-snapshot
Cloning and CO2‐dependent expression of the genetic region for encapsulation from Bacillus anthracis
inferredcites →https://doi.org/10.1111/j.1365-2958.1993.tb01710.xopenalex-snapshot
Identification of a novel gene, dep, associated with depolymerization of the capsular polymer in Bacillus anthracis
inferredcites →https://doi.org/10.1128/aem.69.5.2491-2497.2003openalex-snapshot
Characterization of Poly-γ-Glutamate Hydrolase Encoded by a Bacteriophage Genome: Possible Role in Phage Infection of Bacillus subtilis Encapsulated with Poly-γ-Glutamate
inferredcites →https://doi.org/10.1128/jb.168.3.1325-1331.1986openalex-snapshot
gamma-Glutamyltranspeptidase from Escherichia coli K-12: purification and properties
inferredcites →https://doi.org/10.1128/jb.171.2.722-730.1989openalex-snapshot
Molecular characterization and protein analysis of the cap region, which is essential for encapsulation in Bacillus anthracis
inferredcites →https://doi.org/10.1128/jb.175.18.6038-6040.1993openalex-snapshot
Escherichia coli K-12 can utilize an exogenous gamma-glutamyl peptide as an amino acid source, for which gamma-glutamyltranspeptidase is essential
inferredcites →https://doi.org/10.1128/jb.178.14.4319-4322.1996openalex-snapshot
Identification, sequence, and expression of the gene encoding gamma-glutamyltranspeptidase in Bacillus subtilis
inferredcites →https://doi.org/10.1128/jb.184.12.3377-3384.2002openalex-snapshot
Characterization and Regulation of the gbuA Gene, Encoding Guanidinobutyrase in the Arginine Dehydrogenase Pathway of Pseudomonas aeruginosa PAO1
inferredcites →https://doi.org/10.1128/jb.184.2.337-343.2002openalex-snapshot
Characterization of the Bacillus subtilis ywsC Gene, Involved in γ-Polyglutamic Acid Production
inferredcites →https://doi.org/10.1128/jb.185.7.2379-2382.2003openalex-snapshot
Characterization of the Bacillus subtilis ywtD Gene, Whose Product Is Involved in γ-Polyglutamic Acid Degradation
inferredcites →https://doi.org/10.1128/jb.186.4.1213-1214.2004openalex-snapshot
γ-Glutamyltranspeptidase, but Not YwrD, Is Important in Utilization of Extracellular Glutathione as a Sulfur Source in Bacillus subtilis
inferredcites →https://doi.org/10.1146/annurev.micro.53.1.217openalex-snapshot
DNA Uptake in Bacteria
inferredcites →https://doi.org/10.1271/bbb.57.2148openalex-snapshot
Purification and Characterization of Poly(γ-glutamic acid) Hydrolase from a Filamentous Fungus,Myrotheciumsp. TM-4222
inferredcites →https://doi.org/10.1271/bbb.61.1596openalex-snapshot
DNA Sequence ofBacillus subtilis(natto) NR-1γ-Glutamyltranspeptidase Gene,ggt
inferredcites →https://doi.org/10.1271/bbb.61.1621openalex-snapshot
Purification and Properties of Two Isozymes of γ-Glutamyltranspeptidase fromBacillus subtilisTAM-4
inferredcites →https://doi.org/10.1271/bbb1961.55.2971openalex-snapshot
Purification and Properties of .GAMMA.-Glutamyltranspeptidase from Bacillus subtilis (natto).
inferredcites →https://doi.org/10.2323/jgam.43.139openalex-snapshot
Chemical analysis of poly-.GAMMA.-glutamic acid produced by plasmid-free Bacillus subtilis (natto): Evidence that plasmids are not involved in poly-.GAMMA.-glutamic acid production.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4639636openalex-extracted
Genomic Characterization and Related Functional Genes of Γ-Polyglutamic Acid-Producing Bacillus Subtilis
inferred← citeshttps://doi.org/10.1002/bit.24846openalex-snapshot
Knockout of pgdS and ggt genes improves γ‐PGA yield in B. subtilis
inferred← citeshttps://doi.org/10.1002/btpr.3293openalex-snapshot
Online measurement of the viscosity in shake flasks enables monitoring of γ‐PGA production in depolymerase knockout mutants of Bacillus subtilis with the phosphate‐starvation inducible promoter P pst
inferred← citeshttps://doi.org/10.1002/btpr.417openalex-snapshot
Chromosomal integration of a synthetic expression control sequence achieves poly‐γ‐glutamate production in a Bacillus subtilis strain
inferred← citeshttps://doi.org/10.1002/jctb.4261openalex-snapshot
Enhanced expression of pgdS gene for high production of poly‐γ‐glutamic aicd with lower molecular weight in Bacillus licheniformis WX ‐02
inferred← citeshttps://doi.org/10.1002/jctb.6420openalex-snapshot
Oxygen transfer rate determines molecular weight and production of poly( γ‐ glutamic acid) as well as carbon utilization by Bacillus velezensis 83
inferred← citeshttps://doi.org/10.1002/jsfa.4120openalex-snapshot
Development of efficient enzymatic production of theanine by γ‐glutamyltranspeptidase from a newly isolated strain of Bacillus subtilis, SK11.004
inferred← citeshttps://doi.org/10.1002/jsfa.4635openalex-snapshot
Effects of pH and dissolved oxygen on the synthesis of γ‐glutamyltranspeptidase from Bacillus subtilis SK 11.004
inferred← citeshttps://doi.org/10.1002/prot.23229openalex-snapshot
Crystal structure of bacteriophage ϕNIT1 zinc peptidase PghP that hydrolyzes γ‐glutamyl linkage of bacterial poly‐γ‐glutamate
inferred← citeshttps://doi.org/10.1007/978-3-031-06600-9_9openalex-snapshot
Recent Advances in Poly-(γ-Glutamic Acid) Production by Microbial Fermentation
inferred← citeshttps://doi.org/10.1007/978-3-642-12453-2_6openalex-snapshot
Enzymatic Degradation of Poly-Gamma-Glutamic Acid
inferred← citeshttps://doi.org/10.1007/s00203-014-1057-0openalex-snapshot
γ-Glutamyl transpeptidase (GgtA) of Aspergillus nidulans is not necessary for bulk degradation of glutathione
inferred← citeshttps://doi.org/10.1007/s00253-009-1894-yopenalex-snapshot
Development of natto with germination-defective mutants of Bacillus subtilis (natto)
inferred← citeshttps://doi.org/10.1007/s00253-014-5729-0openalex-snapshot
Functions of poly-gamma-glutamic acid (γ-PGA) degradation genes in γ-PGA synthesis and cell morphology maintenance
inferred← citeshttps://doi.org/10.1007/s00289-021-03820-9openalex-snapshot
Biopolymer production in microbiology by application of metabolic engineering
inferred← citeshttps://doi.org/10.1007/s10930-006-9025-4openalex-snapshot
Identification and Characterization of a Gamma-Glutamyl Transpeptidase from a Thermo-Alcalophile Strain of Bacillus pumilus
inferred← citeshttps://doi.org/10.1007/s11274-018-2443-6openalex-snapshot
Regulatory phosphorylation of poly-γ-glutamic acid with phosphate salts in the culture of Bacillus subtilis (natto)
inferred← citeshttps://doi.org/10.1007/s11274-022-03364-8openalex-snapshot
Structural and genetic insights into a poly-γ-glutamic acid with in vitro antioxidant activity of Bacillus velezensis VCN56
inferred← citeshttps://doi.org/10.1007/s11515-014-1288-0openalex-snapshot
Gamma-glutamyl transferases: A structural, mechanistic and physiological perspective
inferred← citeshttps://doi.org/10.1007/s12010-017-2654-6openalex-snapshot
Selection of an Effective Indicator for Rapid Detection of Microorganisms Producing γ-Polyglutamic Acid and Its Biosynthesis Under Submerged Fermentation Conditions Using Bacillus methylotrophicus
inferred← citeshttps://doi.org/10.1007/s13399-021-01467-0openalex-snapshot
Poly-gamma-glutamic acid biopolymer: a sleeping giant with diverse applications and unique opportunities for commercialization
inferred← citeshttps://doi.org/10.1007/s40710-016-0161-3openalex-snapshot
Glutamic Acid Independent Production of Bioflocculants by Bacillus subtilis UPMB13
inferred← citeshttps://doi.org/10.1016/b978-0-12-396983-5.00003-xopenalex-snapshot
Proteins and Poly(Amino Acids)
inferred← citeshttps://doi.org/10.1016/b978-0-12-820084-1.00026-0openalex-snapshot
Biosynthesis of polyglutamic acid (γ-PGA), a biodegradable and economical polyamide biopolymer for industrial applications
inferred← citeshttps://doi.org/10.1016/b978-0-12-821888-4.00021-6openalex-snapshot
Production and applications of polyglutamic acid
inferred← citeshttps://doi.org/10.1016/b978-0-443-33524-2.00004-1openalex-snapshot
Types of microbial biopolymers
inferred← citeshttps://doi.org/10.1016/b978-0-443-33524-2.00006-5openalex-snapshot
Biopolymer composites
inferred← citeshttps://doi.org/10.1016/b978-0-444-63662-1.00030-0openalex-snapshot
Production and Application of Poly-γ-glutamic Acid
inferred← citeshttps://doi.org/10.1016/j.biortech.2011.02.047openalex-snapshot
Poly (glutamic acid) – An emerging biopolymer of commercial interest
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2018.05.006openalex-snapshot
Genetic and metabolic engineering for microbial production of poly-γ-glutamic acid
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2022.108049openalex-snapshot
Building a circular economy around poly(D/L-γ-glutamic acid)- a smart microbial biopolymer
inferred← citeshttps://doi.org/10.1016/j.cdc.2020.100538openalex-snapshot
Green synthesis, characterization, catalytic and antibacterial studies of copper iodide nanoparticles synthesized using Brassica oleracea var. capitata f. rubra extract
inferred← citeshttps://doi.org/10.1016/j.colsurfb.2012.03.021openalex-snapshot
A novel study of antibacterial activity of copper iodide nanoparticle mediated by DNA and membrane damage
inferred← citeshttps://doi.org/10.1016/j.envres.2021.111759openalex-snapshot
Effect of shape and anthocyanin capping on antibacterial activity of CuI particles
inferred← citeshttps://doi.org/10.1016/j.enzmictec.2011.08.005openalex-snapshot
γ-Glutamyl transpeptidase from Bacillus pumilus KS 12: Decoupling autoprocessing from catalysis and molecular characterization of N-terminal region
inferred← citeshttps://doi.org/10.1016/j.enzmictec.2018.04.001openalex-snapshot
Evidences on the role of the lid loop of γ-glutamyltransferases (GGT) in substrate selection
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.09.020openalex-snapshot
Targeting gamma-glutamyl transpeptidase: A pleiotropic enzyme involved in glutathione metabolism and in the control of redox homeostasis
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2014.12.017openalex-snapshot
Purification and characterization of gamma poly glutamic acid from newly Bacillus licheniformis NRC20
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2016.03.007openalex-snapshot
Branched chain amino acids maintain the molecular weight of poly(γ-glutamic acid) of Bacillus licheniformis ATCC 9945 during the fermentation
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2019.05.014openalex-snapshot
Poly-γ-glutamic acid production of Bacillus subtilis (natto) in the absence of DegQ: A gain-of-function mutation in yabJ gene
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2019.08.003openalex-snapshot
Knockout of pgdS and ggt gene changes poly-γ-glutamic acid production in Bacillus licheniformis RK14-46
inferred← citeshttps://doi.org/10.1016/j.lwt.2019.108811openalex-snapshot
Sterilization of Bacillus tequilensis isolated from aerogenic vinegar by intense pulsed light
inferred← citeshttps://doi.org/10.1016/j.molcatb.2006.06.021openalex-snapshot
Production, purification and properties of γ-glutamyltranspeptidase from a newly isolated Bacillus subtilis NX-2
inferred← citeshttps://doi.org/10.1016/j.molcatb.2007.12.027openalex-snapshot
Investigation on enzymatic degradation of γ-polyglutamic acid from Bacillus subtilis NX-2
inferred← citeshttps://doi.org/10.1016/j.myc.2016.07.002openalex-snapshot
Characterization of extracellular γ-glutamyl transpeptidase from Aspergillus nidulans
inferred← citeshttps://doi.org/10.1016/j.procbio.2017.02.017openalex-snapshot
Improved production of poly-γ-glutamic acid with low molecular weight under high ferric ion concentration stress in Bacillus licheniformis ATCC 9945a
inferred← citeshttps://doi.org/10.1016/j.procbio.2019.11.034openalex-snapshot
A newly isolated Bacillus siamensis SB1001 for mass production of poly-γ-glutamic acid
inferred← citeshttps://doi.org/10.1016/j.ymben.2019.08.011openalex-snapshot
Engineering Corynebacterium glutamicum for the de novo biosynthesis of tailored poly-γ-glutamic acid
inferred← citeshttps://doi.org/10.1021/acs.biomac.3c01000openalex-snapshot
Peptide Epimerase Responsible for d -Amino Acid Introduction in Poly-γ-glutamic Acid Biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c06139openalex-snapshot
Identification and Activity Characterization of γ-Glutamyltransferase from Bovine Milk
inferred← citeshttps://doi.org/10.1021/jf2003249openalex-snapshot
Purification and Characterization of γ-Glutamyltranspeptidase from Bacillus subtilis SK11.004
inferred← citeshttps://doi.org/10.1039/c9ra05941eopenalex-snapshot
Effect of the inserted active-site-covering lid loop on the catalytic activity of a mutant B. subtilis γ-glutamyltransferase (GGT)
inferred← citeshttps://doi.org/10.1049/mnl.2014.0014openalex-snapshot
Antibacterial mechanisms of silica/polydopamine/silver nanoparticles against gram positive and gram negative bacteria
inferred← citeshttps://doi.org/10.1074/jbc.m109.019034openalex-snapshot
Crystal Structure of Bacillus anthracis Transpeptidase Enzyme CapD
inferred← citeshttps://doi.org/10.1080/07388550601166458openalex-snapshot
Microbial Biosynthesis of Polyglutamic Acid Biopolymer and Applications in the Biopharmaceutical, Biomedical and Food Industries
inferred← citeshttps://doi.org/10.1080/07388551.2026.2666082openalex-snapshot
Tuning molecular weight of poly-γ-glutamic acid: advanced biosynthetic engineering approaches and diversified applications
inferred← citeshttps://doi.org/10.1093/bbb/zbaa037openalex-snapshot
Tetramer formation of Bacillus subtilis YabJ protein that belongs to YjgF/YER057c/UK114 family
inferred← citeshttps://doi.org/10.1093/bbb/zbaf194openalex-snapshot
L-γ-polyglutamate in Bacillus : stereocontrol by the PgsA epimerase and selective γ-PGA hydrolases
inferred← citeshttps://doi.org/10.1094/mpmi-21-9-1261openalex-snapshot
Transposon Mutagenesis Reveals Differential Pathogenesis of Ralstonia solanacearum on Tomato and Arabidopsis
inferred← citeshttps://doi.org/10.1099/mic.0.035857-0openalex-snapshot
Capsule depolymerase overexpression reduces Bacillus anthracis virulence
inferred← citeshttps://doi.org/10.1099/mic.0.081448-0openalex-snapshot
Poly-γ-glutamic acid: production, properties and applications
inferred← citeshttps://doi.org/10.1111/1751-7915.12136openalex-snapshot
Metabolic engineering of B acillus amyloliquefaciens for poly‐gamma‐glutamic acid (γ‐ PGA ) overproduction
inferred← citeshttps://doi.org/10.1111/febs.12591openalex-snapshot
pH‐Dependent hydrolase, glutaminase, transpeptidase and autotranspeptidase activities of Bacillus subtilis γ‐glutamyltransferase
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2005.04718.xopenalex-snapshot
Bacillus anthracis CapD, belonging to the γ‐glutamyltranspeptidase family, is required for the covalent anchoring of capsule to peptidoglycan
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2006.05099.xopenalex-snapshot
Streptococcus gordonii utilizes several distinct gene functions to recruit Porphyromonas gingivalis into a mixed community
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2006.05179.xopenalex-snapshot
Poly‐gamma‐glutamate in bacteria
inferred← citeshttps://doi.org/10.1111/j.1365-2958.2008.06533.xopenalex-snapshot
Capsule anchoring in Bacillus anthracis occurs by a transpeptidation reaction that is inhibited by capsidin
inferred← citeshttps://doi.org/10.1111/mmi.12523openalex-snapshot
A poly‐γ‐ d ‐glutamic acid depolymerase that degrades the protective capsule of B acillus anthracis
inferred← citeshttps://doi.org/10.1117/12.2218040openalex-snapshot
Single molecule force spectroscopy study of γ-polyglutamic acid by using atomic force microscopy
inferred← citeshttps://doi.org/10.1128/9781555817107.ch21openalex-snapshot
HeterotypicStreptococcus gordonii‐Porphyromonas gingivalisCommunities: Formation, Gene Regulation, and Development
inferred← citeshttps://doi.org/10.1128/aem.00147-07openalex-snapshot
Plant Cell Wall Degradation by Saprophytic Bacillus subtilis Strains: Gene Clusters Responsible for Rhamnogalacturonan Depolymerization
inferred← citeshttps://doi.org/10.1128/aem.00448-11openalex-snapshot
Phylogenetic Analysis of Bacillus subtilis Strains Applicable to Natto (Fermented Soybean) Production
inferred← citeshttps://doi.org/10.1128/aem.05827-11openalex-snapshot
Mutations Suppressing the Loss of DegQ Function in Bacillus subtilis (natto) Poly-γ-Glutamate Synthesis
inferred← citeshttps://doi.org/10.1155/2014/216270openalex-snapshot
Effect of pH on the Hydrolytic Kinetics of Gamma-Glutamyl Transferase from Bacillus subtilis
inferred← citeshttps://doi.org/10.1186/s12866-018-1205-9openalex-snapshot
Whole genome sequencing and identification of Bacillus endophyticus and B. anthracis isolated from anthrax outbreaks in South Africa
inferred← citeshttps://doi.org/10.1186/s13068-016-0537-7openalex-snapshot
Microbial synthesis of poly-γ-glutamic acid: current progress, challenges, and future perspectives
inferred← citeshttps://doi.org/10.1263/jbb.102.60openalex-snapshot
Novel poly-γ-glutamate-processing enzyme catalyzing γ-glutamyl DD-amidohydrolysis
inferred← citeshttps://doi.org/10.1271/bbb.60108openalex-snapshot
Structure of the Hydrolyzed Product (F-2) Released from γ-Polyglutamic Acid by γ-Glutamyl Hydrolase YwtD ofBacillus subtilis
inferred← citeshttps://doi.org/10.1271/bbb.70223openalex-snapshot
Determination and Characterization of IS4Bsu1-Insertion Loci and Identification of a New Insertion Sequence Element of the IS256Family in a Natto Starter
inferred← citeshttps://doi.org/10.1271/bbb.80913openalex-snapshot
Expression of thepgsBEncoding the Poly-gamma- DL -glutamate Synthetase ofBacillus subtilis (natto)
inferred← citeshttps://doi.org/10.12938/bmfh.2021-084openalex-snapshot
Combination of poly-γ-glutamic acid and galactooligosaccharide improves intestinal microbiota, defecation status, and relaxed mood in humans: a randomized, double-blind, parallel-group comparison trial
inferred← citeshttps://doi.org/10.13141/jve.vol9.no1.pp49-54openalex-snapshot
Isolation, characterization of Bacillus sp. producing heavy metal absorption γ-PGA
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011295openalex-snapshot
Adaptations to nitrogen availability drive ecological divergence of chemosynthetic symbionts
inferred← citeshttps://doi.org/10.1371/journal.pone.0130810openalex-snapshot
γ-PGA Hydrolases of Phage Origin in Bacillus subtilis and Other Microbial Genomes
inferred← citeshttps://doi.org/10.1371/journal.pone.0141369openalex-snapshot
Whole-Genome Sequencing and Comparative Genome Analysis of Bacillus subtilis Strains Isolated from Non-Salted Fermented Soybean Foods
inferred← citeshttps://doi.org/10.1371/journal.pone.0222322openalex-snapshot
Antibacterial activity of silver nanoparticles of different particle size against Vibrio Natriegens
inferred← citeshttps://doi.org/10.1556/018.66.2015.2.10openalex-snapshot
Degradation of glutathione inAspergillus nidulans— Short communication
inferred← citeshttps://doi.org/10.2166/wst.2014.329openalex-snapshot
Solid-state fermentation of soybean residues for bioflocculant production in a pilot-scale bioreactor system
inferred← citeshttps://doi.org/10.2174/1874285802014010030openalex-snapshot
Production of Poly-γ-Glutamic Acid (γ-PGA) by Clinical Isolates of Staphylococcus Epidermidis
inferred← citeshttps://doi.org/10.22207/jpam.13.2.03openalex-snapshot
Comparative Genome Assessment of the Two Novel Poly-γ-Glutamic Acid Producing Bacillus Strains
inferred← citeshttps://doi.org/10.22207/jpam.13.2.10openalex-snapshot
Coherent Aspects of Multifaceted Eco-friendly Biopolymer - Polyglutamic Acid from the Microbes
inferred← citeshttps://doi.org/10.2323/jgam.57.35openalex-snapshot
Disruption of the cell wall lytic enzyme CwlO affects the amount and molecular size of poly-γ-glutamic acid produced by Bacillus subtilis (natto)
inferred← citeshttps://doi.org/10.3109/07388551.2012.743501openalex-snapshot
Recent Advances in Microbial Biopolymer Production and Purification
inferred← citeshttps://doi.org/10.3136/fstr.17.447openalex-snapshot
Loss of poly-.GAMMA.-glutamic Acid Synthesis of Bacillus subtilis (natto) Due to IS4Bsu1 Translocation to swrA Gene
inferred← citeshttps://doi.org/10.3136/fstr.27.497openalex-snapshot
Storage temperature and quality changes of natto
inferred← citeshttps://doi.org/10.3136/fstr.fstr-d-21-00312openalex-snapshot
Isolation and characterization of Bacillus subtilis from commercially available honey and its application in natto fermentation
inferred← citeshttps://doi.org/10.3136/nskkk.57.479openalex-snapshot
The Quality of Natto Produced by the Sporulation Mutants of Bacillus subtilis (natto)
inferred← citeshttps://doi.org/10.3136/nskkk.60.577openalex-snapshot
Black Soybean Fermentation using a rpoB Mutant Strain of Bacillus subtilis (natto)
inferred← citeshttps://doi.org/10.3389/fmicb.2015.00567openalex-snapshot
The Campylobacter jejuni RacRS two-component system activates the glutamate synthesis by directly upregulating γ-glutamyltranspeptidase (GGT)
inferred← citeshttps://doi.org/10.3389/fmicb.2021.641251openalex-snapshot
Bacterial Gamma-Glutamyl Transpeptidase, an Emerging Biocatalyst: Insights Into Structure–Function Relationship and Its Biotechnological Applications
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1348411openalex-snapshot
Poly (γ) glutamic acid: a unique microbial biopolymer with diverse commercial applicability
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1597704openalex-snapshot
Construction of an engineered Bacillus subtilis for production of poly-γ-glutamic acids with specific molecular weights
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1647287openalex-snapshot
Microbial production and functional assessment of γ-polyglutamic acid isolated from Bacillus sp. M-E6
inferred← citeshttps://doi.org/10.3389/fpls.2024.1344383openalex-snapshot
Genotype-specific germination behavior induced by sustainable priming techniques in response to water deprivation stress in rice
inferred← citeshttps://doi.org/10.3390/books978-3-03842-178-8openalex-snapshot
Extremophiles and Extreme Environments
inferred← citeshttps://doi.org/10.3390/foods11050739openalex-snapshot
Recent Advances in Microbial Synthesis of Poly-γ-Glutamic Acid: A Review
inferred← citeshttps://doi.org/10.3390/ijms18122644openalex-snapshot
Poly-γ-glutamic Acid Synthesis, Gene Regulation, Phylogenetic Relationships, and Role in Fermentation
inferred← citeshttps://doi.org/10.3390/life3010181openalex-snapshot
Pivotal Enzyme in Glutamate Metabolism of Poly-g-Glutamate-Producing Microbes
inferred← citeshttps://doi.org/10.3390/polym14142937openalex-snapshot
Microbial Poly-γ-Glutamic Acid (γ-PGA) as an Effective Tooth Enamel Protectant
inferred← citeshttps://doi.org/10.5483/bmbrep.2005.38.5.609openalex-snapshot
The Gene Encoding γ-Glutamyl Transpeptidase II in the Fission Yeast Is Regulated by Oxidative and Metabolic Stress
inferred← citeshttps://doi.org/10.55251/jmbfs.10075openalex-snapshot
POLY-GAMMA-GLUTAMIC ACID: A COMPREHENSIVE OVERVIEW OF BIOSYNTHESIS, CHARACTERISTICS, AND EMERGING APPLICATIONS
inferred← citeshttps://doi.org/10.6090/jarq.52.249openalex-snapshot
Poly-γ-glutamic Acid Production by Bacillus subtilis (natto) under High Salt Conditions
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.