Nik operon

The nik operon is an operon required for uptake of nickel ions into the cell. It is present in many bacteria, but has been extensively studied in Helicobacter pylori. Nickel is an essential nutrient for many microorganisms, where it participates in a variety of cellular processes. However, excessive levels of nickel ions in cell can be fatal to the cell. Nickel ion concentration in the cell is regulated through the nik operon.

Structure of the ''nik'' operon

The nik operon consists of six genes. The first five genes nikABCDE encode components of a typical ABC transport system and the last gene nikR encodes a DNA-binding protein that represses transcription of nikABCDE when sufficient Ni²⁺ is present. The nikR gene is located 5 bp downstream of the end of nikE, transcribed in the same direction as nikABCDE. The following table summarizes the structure of the nik operon:

Gene	Protein encoded	Functional Role
nikA	ABC transporter Ni²⁺binding component	binds Ni²⁺ in the periplasm and transfers it to the permease; may also play a role in chemotaxis away from toxic concentrations of nickel
nikB & nikC	ABC transporter permease components	transport of Ni²⁺+ across the inner membrane
nikD & nikE	ABC transporter ATP-binding components	hydrolyzes ATP to provide energy for the transport process
nikR	transcriptional regulator of the nikABCDE operon	downregulates expression of the nik operon in the presence of excess Ni²⁺ ions

Regulation

''nikR'' Regulation

Regulation of expression of the nikR gene is achieved by two promoters. The first is through the FNR regulon. The FNR controlled regulation of nikABCDE–nikR occurs at a FNR box located upstream of nikA at a putative NikR binding site. The second promoter element regulating nikR expression occurs 51 bp upstream of the nikR transcription start site and results in low-level constitutive expression. There is also evidence that nikR expression is partially autoregulated.

Regulation of Ni²⁺ uptake

Ni²⁺ is taken up into prokaryotic cells by one of two types of high-affinity transport systems. The first method involves ABC-type transporters and the second mechanism makes use of transition-metal permeases. The ABC-type transporter system consists of five proteins, NikA–E, that carry out the ATP-dependent transport of Ni²⁺. NikA is a soluble, periplasmic, Ni-binding protein; NikB and NikC form a transmembrane pore for passage of Ni; and NikD and NikE hydrolyze ATP and couple this energy to Ni²⁺-transport. When Ni²⁺ is available in excess, NikR protein represses transcription of nikABCDE.

Repression by NikR binding

Using profile-based sequence database searches, NikR was shown to be a member of the ribbon-helix-helix family of transcription factors. It has been demonstrated that the N-terminal domain of NikR is responsible for binding to DNA and that it only binds in presence of Ni²⁺. NikR has two sites for binding to Ni²⁺ ions. Binding of Ni²⁺ at concentrations that allow full occupancy of only the high-affinity sites is sufficient for operator binding, but the affinity for the operator is increased 1000-fold and the operator footprints are larger when both nickel-binding sites are occupied. These results, combined with estimates of intracellular Ni²⁺ and NikR concentrations, lead to the conclusion that NikR is able to sense Ni²⁺ and regulate the nik operon expression over a range of intracellular Ni²⁺ concentrations from as low as one to as high as 10,000 molecules per cell.