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Optimization of arsB (Acr3) as a positive selection marker in the cyanobacterium Synechocystis sp. PCC 6803
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0061(199707)13:9<819::aid-yea142>3.0.co;2-yopenalex-snapshot
Isolation of Three Contiguous Genes,ACR1,ACR2 andACR3, Involved in Resistance to Arsenic Compounds in the YeastSaccharomyces cerevisiae
inferredcites →https://doi.org/10.1007/s00253-013-4838-5openalex-snapshot
Bacterial metabolism of environmental arsenic—mechanisms and biotechnological applications
inferredcites →https://doi.org/10.1007/s11120-006-9093-5openalex-snapshot
The diversity and complexity of the cyanobacterial thioredoxin systems
inferredcites →https://doi.org/10.1007/s11120-014-9980-0openalex-snapshot
Engineering cyanobacteria as photosynthetic feedstock factories
inferredcites →https://doi.org/10.1016/0378-1119(88)90605-1openalex-snapshot
A versatile class of positive-selection vectors based on the nonviability of palindrome-containing plasmids that allows cloning into long polylinkers
inferredcites →https://doi.org/10.1016/j.bbabio.2012.08.007openalex-snapshot
Arsenics as bioenergetic substrates
inferredcites →https://doi.org/10.1016/j.bj.2015.08.003openalex-snapshot
New mechanisms of bacterial arsenic resistance
inferredcites →https://doi.org/10.1016/j.copbio.2017.07.008openalex-snapshot
Systems and synthetic biology for the biotechnological application of cyanobacteria
inferredcites →https://doi.org/10.1016/j.envint.2019.02.058openalex-snapshot
Pathways of arsenic uptake and efflux
inferredcites →https://doi.org/10.1016/j.envpol.2017.05.005openalex-snapshot
Arsenic biotransformation by a cyanobacterium Nostoc sp. PCC 7120
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2011.04.008openalex-snapshot
Arsenic-induced oxidative stress and its reversibility
inferredcites →https://doi.org/10.1016/j.jmb.2006.07.002openalex-snapshot
Arsenate Reduction: Thiol Cascade Chemistry with Convergent Evolution
inferredcites →https://doi.org/10.1016/j.tibtech.2018.05.011openalex-snapshot
CRISPR-Based Technologies for Metabolic Engineering in Cyanobacteria
inferredcites →https://doi.org/10.1016/j.tplants.2011.12.003openalex-snapshot
Arsenic biomethylation by photosynthetic organisms
inferredcites →https://doi.org/10.1016/s0966-842x(99)01494-8openalex-snapshot
Families of arsenic transporters
inferredcites →https://doi.org/10.1017/s0033583512000157openalex-snapshot
Why nature really chose phosphate
inferredcites →https://doi.org/10.1021/acs.est.5b03357openalex-snapshot
Arsenic Demethylation by a C·As Lyase in Cyanobacterium Nostoc sp. PCC 7120
inferredcites →https://doi.org/10.1021/acs.est.6b04952openalex-snapshot
Arsenic Methyltransferase is Involved in Arsenosugar Biosynthesis by Providing DMA
inferredcites →https://doi.org/10.1021/acs.est.7b03180openalex-snapshot
Biochemical Characterization of ArsI: A Novel C–As Lyase for Degradation of Environmental Organoarsenicals
inferredcites →https://doi.org/10.1021/acs.est.8b04389openalex-snapshot
Identification of Steps in the Pathway of Arsenosugar Biosynthesis
inferredcites →https://doi.org/10.1021/bi200002aopenalex-snapshot
Arsenate Replacing Phosphate: Alternative Life Chemistries and Ion Promiscuity
inferredcites →https://doi.org/10.1021/bi201904popenalex-snapshot
ArsH from the CyanobacteriumSynechocystissp. PCC 6803 Is an Efficient NADPH-Dependent Quinone Reductase
inferredcites →https://doi.org/10.1021/es403836gopenalex-snapshot
Cyanobacteria-Mediated Arsenic Redox Dynamics Is Regulated by Phosphate in Aquatic Environments
inferredcites →https://doi.org/10.1039/c6mt00168hopenalex-snapshot
The organoarsenical biocycle and the primordial antibiotic methylarsenite
inferredcites →https://doi.org/10.1046/j.1365-2958.2001.02485.xopenalex-snapshot
The glycerol channel Fps1p mediates the uptake of arsenite and antimonite in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.092131899openalex-snapshot
Arsenite transport by mammalian aquaglyceroporins AQP7 and AQP9
inferredcites →https://doi.org/10.1073/pnas.1403057111openalex-snapshot
A C⋅As lyase for degradation of environmental organoarsenical herbicides and animal husbandry growth promoters
inferredcites →https://doi.org/10.1073/pnas.2001063117openalex-snapshot
The Great Oxidation Event expanded the genetic repertoire of arsenic metabolism and cycling
inferredcites →https://doi.org/10.1074/jbc.m400037200openalex-snapshot
As(III) and Sb(III) Uptake by GlpF and Efflux by ArsB in Escherichia coli
inferredcites →https://doi.org/10.1093/nar/gku673openalex-snapshot
Broad-host-range vector system for synthetic biology and biotechnology in cyanobacteria
inferredcites →https://doi.org/10.1104/pp.111.178947openalex-snapshot
Biotransformation and Volatilization of Arsenic by Three Photosynthetic Cyanobacteria
inferredcites →https://doi.org/10.1111/1462-2920.14991openalex-snapshot
ArsH protects Pseudomonas putida from oxidative damage caused by exposure to arsenic
inferredcites →https://doi.org/10.1111/mmi.12988openalex-snapshot
ArsH is an organoarsenical oxidase that confers resistance to trivalent forms of the herbicide monosodium methylarsenate and the poultry growth promoter roxarsone
inferredcites →https://doi.org/10.1111/mmi.13145openalex-snapshot
ArsP : a methylarsenite efflux permease
inferredcites →https://doi.org/10.1111/mmi.13371openalex-snapshot
Synergistic interaction of glyceraldehydes‐3‐phosphate dehydrogenase and ArsJ, a novel organoarsenical efflux permease, confers arsenate resistance
inferredcites →https://doi.org/10.1111/mmi.14169openalex-snapshot
The antibiotic action of methylarsenite is an emergent property of microbial communities
inferredcites →https://doi.org/10.1126/science.aba1510openalex-snapshot
Global threat of arsenic in groundwater
inferredcites →https://doi.org/10.1128/aem.01842-18openalex-snapshot
Efflux Transporter ArsK Is Responsible for Bacterial Resistance to Arsenite, Antimonite, Trivalent Roxarsone, and Methylarsenite
inferredcites →https://doi.org/10.1128/jb.00258-10openalex-snapshot
Functional Characterization of Synechocystis sp. Strain PCC 6803 pst1 and pst2 Gene Clusters Reveals a Novel Strategy for Phosphate Uptake in a Freshwater Cyanobacterium
inferredcites →https://doi.org/10.1128/jb.01798-08openalex-snapshot
The Glutathione/Glutaredoxin System Is Essential for Arsenate Reduction in Synechocystis sp. Strain PCC 6803
inferredcites →https://doi.org/10.1128/jb.179.3.612-619.1997openalex-snapshot
Virulence and arsenic resistance in Yersiniae
inferredcites →https://doi.org/10.1128/jb.185.18.5363-5371.2003openalex-snapshot
Arsenic Sensing and Resistance System in the Cyanobacterium Synechocystis sp. Strain PCC 6803
inferredcites →https://doi.org/10.1128/mmbr.00035-08openalex-snapshot
Ecological Genomics of Marine Picocyanobacteria
inferredcites →https://doi.org/10.1146/annurev-earth-060313-054942openalex-snapshot
Earth Abides Arsenic Biotransformations
inferredcites →https://doi.org/10.1146/annurev-micro-020518-120134openalex-snapshot
Membrane Dynamics in Phototrophic Bacteria
inferredcites →https://doi.org/10.1371/journal.pone.0096826openalex-snapshot
Genomic Responses to Arsenic in the Cyanobacterium Synechocystis sp. PCC 6803
inferredcites →https://doi.org/10.3389/fmicb.2011.00214openalex-snapshot
Arsenate Resistance in the Unicellular Marine Diazotroph Crocosphaera watsonii
inferredcites →https://doi.org/10.3389/fmicb.2017.00060openalex-snapshot
Co-expression of Cyanobacterial Genes for Arsenic Methylation and Demethylation in Escherichia coli Offers Insights into Arsenic Resistance
inferredcites →https://doi.org/10.3389/fmicb.2018.02473openalex-snapshot
Distribution of Arsenic Resistance Genes in Prokaryotes
inferredcites →https://doi.org/10.3390/life4040865openalex-snapshot
Metals in Cyanobacteria: Analysis of the Copper, Nickel, Cobalt and Arsenic Homeostasis Mechanisms
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