GO:0015411 ABC-type taurine transporter transporter activity: Mechanism, Genes and Research Methods

Research-grade guide for scientists and biopharma professionals

Key Takeaways

GO:0015411 describes an ATP-binding cassette (ABC) transporter activity that moves taurine across a membrane using ATP hydrolysis.
The reaction is ATP + H2O + taurine(out) = ADP + phosphate + taurine(in), coupling transport to nucleotide hydrolysis.
In Escherichia coli, taurine can serve as a sulfur source, and a sulfate starvation-regulated gene cluster is required for taurine utilization.
The term is a molecular_function annotation, distinct from taurine metabolic processes and from passive taurine transport.
ABC-type taurine transporters are relevant to sulfur metabolism, osmolyte handling, and microbial nutrient acquisition.
CRISPR knockout, point-mutation, knock-in, and overexpression models allow causal testing of candidate transporter genes.

Description

GO:0015411, ABC-type taurine transporter transporter activity, is a molecular_function term describing an ATP-driven transport activity that moves taurine from one side of a membrane to the other. The activity is defined by the coupled reaction ATP + H2O + taurine(out) = ADP + phosphate + taurine(in), meaning that taurine import is energetically linked to ATP hydrolysis. This places the term within the broader class of ATPase-coupled transporters, often called ABC transporters, which use nucleotide binding and hydrolysis to drive substrate translocation. Researchers encounter this term when annotating genes that mediate taurine uptake, particularly in bacteria that can use taurine as a sulfur source under sulfate limitation. In Escherichia coli, sulfate starvation-regulated genes include a gene cluster involved in the utilization of taurine as a sulfur source, providing direct experimental evidence that taurine transport and downstream sulfur mobilization are coordinated. Because taurine is a sulfonated amino acid, its uptake and subsequent desulfonation can supply sulfur when inorganic sulfate is scarce. The GO term therefore captures a specific membrane transport function that connects environmental sulfur availability to cellular metabolism. For genome biologists, correct annotation of GO:0015411 helps distinguish ATP-dependent taurine uptake from other taurine-related functions, such as taurine biosynthesis, taurine catabolism, or sodium-dependent taurine transport. This distinction matters when interpreting transcriptomic responses to sulfate starvation, when building metabolic models, and when designing genetic experiments to test whether a candidate gene is causally required for taurine-dependent growth. The term also provides a controlled vocabulary anchor for comparative genomics of sulfur acquisition across microbial taxa.

ABC-type taurine transporter transporter activity At A Glance

GO ID GO:0015411
GO term ABC-type taurine transporter transporter activity
Ontology molecular_function
Synonym ATPase-coupled taurine transporter activity; ATP-dependent taurine transporter activity; taurine ABC transporter; taurine-transporting ATPase activity
Major function ATP-dependent transfer of taurine across a membrane
Reaction ATP + H2O + taurine(out) = ADP + phosphate + taurine(in)
Coupled energy source ATP hydrolysis
Representative organism context Escherichia coli sulfate starvation-regulated taurine utilization gene cluster
Related process context Utilization of taurine as a sulfur source

What Is GO:0015411?

In plain terms, GO:0015411 means a membrane protein system that uses ATP to pull taurine into the cell. The official QuickGO definition states that this activity enables the transfer of taurine from one side of a membrane to the other according to the reaction ATP + H2O + taurine(out) = ADP + phosphate + taurine(in). It is an ATPase-coupled transporter activity, also known as ATP-dependent taurine transporter activity, taurine ABC transporter, or taurine-transporting ATPase activity. The term belongs to the molecular_function ontology and should not be confused with a biological process such as taurine metabolism or with a cellular component such as the plasma membrane. Functionally, the annotation implies three coupled features: taurine recognition, membrane translocation, and ATP hydrolysis. In Escherichia coli, genes in a sulfate starvation-regulated cluster are involved in taurine utilization as a sulfur source, which is consistent with an ATP-dependent taurine uptake step feeding sulfur metabolism.

Why Is ABC-type taurine transporter transporter activity Important in Cell Biology?

GO:0015411 is important because it defines the molecular step by which cells can acquire taurine using ATP, linking membrane transport to sulfur metabolism and nutrient sensing. In bacteria such as Escherichia coli, the ability to use taurine as a sulfur source depends on sulfate starvation-regulated genes, and the taurine transporter activity is a key entry point for that pathway. Accurate annotation of this activity supports functional genomics, metabolic modeling, and experimental design aimed at understanding how cells respond to sulfur limitation. Because the term is a molecular_function annotation, it also helps researchers separate transport from downstream metabolic conversions when interpreting gene expression or mutant phenotypes.
Defines an ATP-dependent route for taurine entry into cells, distinct from passive or ion-gradient-driven transport.
Connects membrane transport to sulfur acquisition when taurine is used as a sulfur source.
Provides a controlled vocabulary term for annotating genes in sulfate starvation-regulated clusters.
Supports comparative genomics of ABC transporters and sulfur metabolism across microbes.
Helps interpret transcriptomic responses to sulfate limitation in Escherichia coli.
Enables causal tests of candidate genes through knockout and complementation experiments.
Aids metabolic model curation by separating transport from taurine catabolism.
Guides experimental design for taurine-dependent growth assays under sulfur-restricted conditions.

Mechanism, Genes and Research Methods

Substrate recognition and binding
In simple terms: The transporter first recognizes taurine and holds it at the membrane.
ABC-type taurine transporter activity begins with specific recognition of taurine at the membrane transport complex. In Escherichia coli, genes in a sulfate starvation-regulated cluster are involved in the utilization of taurine as a sulfur source, implying that taurine is recognized and taken up before sulfur can be mobilized. This substrate recognition step is part of the molecular function defined by GO:0015411, which requires taurine to be transferred from the outside to the inside of the membrane.
ATP binding and hydrolysis
In simple terms: The system burns ATP to power the transport step.
The GO:0015411 definition couples taurine transfer to the reaction ATP + H2O + taurine(out) = ADP + phosphate + taurine(in), meaning ATP hydrolysis provides the energy for transport. This ATPase-coupled mechanism distinguishes the activity from transport modes that do not directly consume ATP. The sulfate starvation-regulated gene cluster in Escherichia coli provides a genetic context in which this ATP-dependent uptake step supports taurine utilization as a sulfur source.
Membrane translocation of taurine
In simple terms: Taurine is moved across the membrane from outside to inside.
According to the QuickGO definition, the activity enables the transfer of taurine from one side of a membrane to the other. The directional reaction taurine(out) to taurine(in) indicates import into the cell. In Escherichia coli, this import step is part of a sulfate starvation-regulated system for using taurine as a sulfur source.
Coupling to sulfur metabolism
In simple terms: Once inside, taurine can be broken down to supply sulfur.
The physiological relevance of GO:0015411 is illustrated by the Escherichia coli gene cluster involved in the utilization of taurine as a sulfur source, which is regulated by sulfate starvation. Taurine transport is therefore upstream of sulfur mobilization from taurine. This coupling explains why the transporter activity is annotated as part of a nutrient acquisition strategy under sulfur limitation.

Key Genes Involved in GO:0015411 ABC-type taurine transporter transporter activity

The genes and proteins most directly associated with GO:0015411 are those in the sulfate starvation-regulated taurine utilization gene cluster of Escherichia coli, as identified in the verified literature.
GeneMajor RoleResearch Relevance
Escherichia coli taurine utilization gene cluster (as reported)Sulfate starvation-regulated genes involved in taurine utilization as a sulfur sourceProvides genetic evidence linking taurine transport to sulfur acquisition
ABC transporter ATPase component (taurine system)ATP binding and hydrolysis to drive taurine transportCore catalytic component of GO:0015411
ABC transporter permease component (taurine system)Membrane translocation of taurineDefines the transport path across the membrane
ABC transporter substrate-binding component (taurine system)Taurine recognition and delivery to the permeaseDetermines substrate specificity
Sulfate starvation-regulated genesCoordinate response to sulfur limitationContext for taurine transporter expression
Taurine catabolism genesMobilize sulfur from taurine after uptakeDownstream of GO:0015411
Escherichia coli sulfate transport genesInorganic sulfate acquisitionComparative context for sulfur source preference
Escherichia coli sulfur metabolism regulatorsControl sulfate starvation responseRegulatory context for taurine utilization
Taurine ABC transporter operon (as reported)Coordinate expression of transport componentsTarget for knockout and expression studies
Taurine-binding protein (as reported)Initial taurine captureTarget for binding assays
Taurine permease (as reported)Transmembrane channel for taurineTarget for transport assays
Taurine ATPase (as reported)Energy couplingTarget for ATPase assays
Sulfur mobilization enzymesRelease sulfur from taurineDownstream metabolic readout
Sulfate starvation response genesGlobal adaptation to low sulfateTranscriptomic context
Escherichia coli taurine utilization locusGenomic region for taurine useLocus for genetic manipulation
Taurine-responsive promotersRegulate gene expressionReporter assay targets

How Is ABC-type taurine transporter transporter activity Regulated?

The expression and activity of the taurine utilization system are regulated by sulfate starvation in Escherichia coli, as shown by the identification of sulfate starvation-regulated genes in a gene cluster involved in the utilization of taurine as a sulfur source. This means that when sulfate is scarce, the cell increases the capacity to acquire and use alternative sulfur sources such as taurine. The regulation is therefore tied to sulfur availability rather than to taurine alone. Researchers studying GO:0015411 should consider sulfur status as a key experimental variable when measuring transporter gene expression or activity.

ABC-type taurine transporter transporter activity and Human Disease

GeneDisease / BiologyPotential Experimental Model
Escherichia coli taurine utilization gene clusterSulfur source utilization and sulfate starvation responseKnockout of cluster genes followed by growth assay with taurine as sole sulfur source
Taurine ABC transporter ATPase componentATP-dependent taurine transportPoint mutation of ATPase catalytic residues and transport assay
Taurine ABC transporter permease componentMembrane translocation of taurineKnockout and complementation with tagged permease
Taurine-binding proteinSubstrate recognitionBinding assays with purified protein and taurine
Sulfate starvation regulatorsRegulation of taurine utilizationReporter gene fusion and transcriptomics
Sulfur metabolism and nutrient acquisition
GO:0015411 is directly linked to the ability of Escherichia coli to use taurine as a sulfur source under sulfate starvation. Disruption of this activity would be expected to impair growth when taurine is the main sulfur source, providing a model for studying nutrient-dependent growth. This has implications for understanding how bacteria adapt to sulfur-limited environments.
Microbial adaptation and host environments
Taurine is abundant in some host environments, and the ability to transport and utilize it as a sulfur source may support microbial adaptation. The sulfate starvation-regulated gene cluster in Escherichia coli provides a genetic framework for testing whether taurine transport contributes to survival in sulfur-restricted niches. Such studies can inform research on microbial nutrient acquisition.
Relevance to transport-related disorders
While the verified literature for GO:0015411 focuses on bacterial taurine utilization, the general principle of ATP-dependent taurine transport is relevant to understanding how cells regulate taurine levels. Researchers can use the bacterial system as a genetically tractable model to dissect the mechanism of ABC-type taurine transport. This mechanistic knowledge can guide hypothesis generation for other systems.

From ABC-type taurine transporter transporter activity-Related Genes to Experimental Models

Research QuestionSuitable Model
Is the taurine transporter gene required for growth on taurine as a sulfur source?CRISPR knockout of the candidate gene in Escherichia coli followed by growth assay
Which residues are essential for ATP hydrolysis and taurine transport?Point mutation of ATPase catalytic residues
Can a tagged transporter be used to monitor localization and interactions?Knock-in of an epitope tag at the endogenous locus
Does overexpression increase taurine uptake and sulfur acquisition?Overexpression of the transporter operon
How does sulfate starvation regulate transporter expression?Transcriptional reporter or RNA-seq under sulfate-limited conditions
Can the transporter be repurposed for taurine-dependent selection?Knock-in of a selectable marker coupled to taurine utilization

How to Study the ABC-type taurine transporter transporter activity Process

MethodWhat It MeasuresTypical Application
CRISPR knockoutLoss of gene functionTest requirement for taurine utilization
Growth assay with taurine as sulfur sourceAbility to use taurine for sulfurPhenotypic validation of transporter genes
RNA-seqTranscript levelsIdentify sulfate starvation-regulated genes
Reporter gene fusionPromoter activityMeasure regulation by sulfate availability
ATPase assayATP hydrolysis rateConfirm energy coupling of transport
Transport assay with radiolabeled taurineTaurine uptakeMeasure transporter activity
ComplementationRestoration of functionConfirm gene identity
Comparative genomicsGene cluster conservationAnnotate GO:0015411 candidates
Genetic knockout and growth phenotyping
CRISPR knockout of genes in the Escherichia coli taurine utilization cluster can test whether the ABC-type taurine transporter activity is required for growth when taurine is the sole sulfur source. Growth assays under sulfate starvation conditions provide a direct phenotypic readout. Complementation with wild-type or mutant alleles can confirm specificity.
Transcriptomics and reporter assays
RNA-seq or transcriptional reporter fusions can measure how sulfate starvation regulates the taurine utilization gene cluster. The original identification of sulfate starvation-regulated genes in Escherichia coli used such approaches to define the gene cluster involved in taurine utilization. These methods help link transporter expression to environmental sulfur status.
Biochemical transport and ATPase assays
Membrane vesicle or purified protein assays can measure ATP-dependent taurine transport and ATP hydrolysis. The GO:0015411 definition provides the expected reaction stoichiometry for such assays. These experiments directly test the molecular function.
Comparative genomics and annotation
Genome-wide annotation using GO:0015411 can identify taurine transporter candidates across microbial genomes. The Escherichia coli sulfate starvation-regulated cluster serves as a reference locus for comparative analysis. This supports functional prediction and experimental prioritization.

How CRISPR Can Be Used to Study GO:0015411 ABC-type taurine transporter transporter activity

Knockout

CRISPR knockout of candidate genes in the Escherichia coli taurine utilization cluster can determine whether the ABC-type taurine transporter activity is essential for growth on taurine as a sulfur source. Loss-of-function mutants can be tested in sulfate-limited media to reveal the contribution of the transporter to sulfur acquisition. Complementation with the wild-type gene restores function and confirms specificity.

Point Mutation

Point mutations in the ATPase domain of the taurine transporter can be introduced to dissect the coupling between ATP hydrolysis and taurine translocation. Such mutants help define catalytic residues required for the reaction ATP + H2O + taurine(out) = ADP + phosphate + taurine(in). Phenotypic analysis under sulfate starvation links molecular defects to physiological function.

Knock-in

Knock-in of epitope tags or fluorescent proteins at the endogenous taurine transporter locus enables localization and interaction studies. Tagged transporters can be used to monitor expression and membrane insertion under sulfate starvation. This approach preserves native regulation of the taurine utilization gene cluster.

Overexpression

Overexpression of the taurine transporter operon can increase taurine uptake and enhance growth when taurine is the limiting sulfur source. This provides a gain-of-function test for the transporter activity. Overexpression combined with transcriptomics can reveal downstream metabolic effects.

How EDITGENE Supports ABC-type taurine transporter transporter activity Research

Researchers studying ABC-type taurine transporter transporter activity-related genes often need to determine whether a candidate gene is causally involved in taurine uptake, sulfur acquisition, or related phenotypes. EDITGENE provides CRISPR-based cell model services that enable knockout, point mutation, knock-in, overexpression, and library screening to test these hypotheses in a controlled genetic background.
Contact EDITGENE today to design your custom CRISPR model for ABC-type taurine transporter transporter activity research.

Frequently Asked Questions About ABC-type taurine transporter transporter activity

GO:0015411 is the Gene Ontology molecular_function term for ABC-type taurine transporter transporter activity, which enables ATP-dependent transfer of taurine across a membrane according to the reaction ATP + H2O + taurine(out) = ADP + phosphate + taurine(in).
It uses ATP hydrolysis to move taurine from one side of a membrane to the other, typically importing taurine into the cell.
In Escherichia coli, genes in a sulfate starvation-regulated cluster are involved in the utilization of taurine as a sulfur source, which includes the taurine transport function.
Taurine can serve as a sulfur source when sulfate is scarce, and the sulfate starvation-regulated gene cluster allows Escherichia coli to use taurine for this purpose.
It is regulated by sulfate starvation, as shown by the identification of sulfate starvation-regulated genes involved in taurine utilization in Escherichia coli.
The reaction is ATP + H2O + taurine(out) = ADP + phosphate + taurine(in).
GO:0015411 is a molecular_function term; it describes a transport activity rather than a whole pathway or process.
Synonyms include ATPase-coupled taurine transporter activity, ATP-dependent taurine transporter activity, taurine ABC transporter, and taurine-transporting ATPase activity.
CRISPR knockout, point mutation, knock-in tagging, overexpression, growth assays with taurine as a sulfur source, and ATPase or transport assays can be used.
Escherichia coli is a key model, where a sulfate starvation-regulated gene cluster is involved in taurine utilization.

Conclusion

GO:0015411, ABC-type taurine transporter transporter activity, defines an ATP-dependent membrane transport function that moves taurine into cells according to the reaction ATP + H2O + taurine(out) = ADP + phosphate + taurine(in). In Escherichia coli, this activity is part of a sulfate starvation-regulated gene cluster that enables taurine to be used as a sulfur source. Accurate annotation and experimental dissection of this term support studies of sulfur metabolism, nutrient acquisition, and ABC transporter mechanism. CRISPR-based knockout, point-mutation, knock-in, and overexpression models provide direct ways to test the causal role of candidate genes in this activity.

References

  1. 1. van der Ploeg JR et al.. 1996. Identification of sulfate starvation-regulated genes in Escherichia coli: a gene cluster involved in the utilization of taurine as a sulfur source.. J Bacteriol 178(18):5438-46 PMID: 8808933
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