Nitrilase

Nitrilase was first discovered in the early 1960s for its ability to catalyze the hydration of a nitrile to a carboxylic acid.[2] Although it was known at the time that nitrilase could operate with wide substrate specificity in producing the corresponding acid, later studies reported the first NHase (nitrile hydratase) activity exhibited by nitrilase.[3][4] That is, amide compounds could also be formed via nitrile hydrolysis. Further research has revealed several conditions that promote amide formation, which are outlined below.[4]

• Early release of the enzyme-bound substrate after the first water hydrolysis followed by delayed addition of the second water
• Low temperature and increased pH conditions. For bioconversions by nitrilase for most bacteria and fungi, the optimal pH range is between 7.0-8.0 and the optimal temperature range is between 30 and 50 °C.
• Electron withdrawing groups at the ⍺-position

The conversion of a general nitrile to either an amide or carboxylic acid is facilitated by nitrilase.[5][1]

Below is a list of steps involved in transforming a generic nitrile compound with nitrilase:[4]

1. The electrophilic carbon of the nitrile is subject to nucleophilic attack by one of the two SH groups on nitrilase.
2. The thioimidate formed is subsequently hydrolyzed to the acylenzyme and ammonia is created as a byproduct.
3. The acylenzyme can undergo one of two pathways depending on the conditions highlighted above:
   • Further hydrolyzation of the acylenzyme with water produces the carboxylic acid and the regenerated enzyme.
   • The acylenzyme is hydrolyzed by ammonia, displacing the enzyme and forming the amide product.

The active site of a thermoactive nitrilase from Pyrococcus abyssi, detailing the Lys-Cys-Glu catalytic triad responsible for cleaving C-N bonds. Unfortunately, attempts to crystallize the enzyme with either fumaro- or malononitrile have been ineffective so the binding motif remains unknown.[6]

Most nitrilases are made up of a single polypeptide ranging from 32 to 45 kDa,[7] and its structure is an ⍺-β-β-⍺ fold.[4] The favored form of the enzyme is a large filament consisting of 6-26 subunits.[7] Nitrilase exploits the Lys-Cys-Glu catalytic triad which is essential for its active site function and enhancing its performance.[4][7]

The structure of a thermoactive nitrilase from P. abyssi consists of a 2-fold symmetric dimer in which each subunit contains 262 residues.[8][9] Similar to other nitrilases in the nitrilase family, each subunit has an ⍺-β-β-⍺ sandwich fold; when the two subunits come together and interact, the protein forms a ‘super-sandwich’ (⍺-β-β-⍺-⍺-β-β-⍺) structure.[6] In order to dimerize, the C-terminals of each subunit extend out from the core and interact with each other, and this is largely made possible by the salt bridges formed between arginine and glutamate residues.[6]

Although the exact binding mechanism to the nitrile substrate still remains unknown, by drawing comparisons between the sequence and structure with other nitrilases, the catalytic triad was determined to consist of Glu 42, Lys 113, and Cys 146.[6][4][7] With the aid of protein modeling programs, Glu 42 was observed to be the catalytic base in activating the nucleophile (Cys 146) based on the relatively short distance between the O in Glu and S in Cys. Likewise, Lys 113 was inferred to be the catalytic acid responsible for proton transfer to the substrate.[8][10]

Nitrilases have critical roles in plant-microbe interactions for defense, detoxification, nitrogen utilization, and plant hormone synthesis.[11] In plants, there are two distinguishable groups in regard to substrate specificity: those with high hydrolytic activity towards arylacetonitriles and those with high activity towards β-cyano-L-alanine. NIT1, 2, and 3 of the A. thaliana species are examples of the first group of plant nitrilases (arylacetonitrilases) which hydrolyze the nitriles produced during the synthesis or degradation of cyanogenic glycosides and glucosinolates. The arylcetonitrile substrates for these particular enzymes consist of phenylpropionitrile and other products that result from glucosinolate metabolism.[11][12] NIT4 however, belongs to the second group of plant nitrilases and is critical for cyanide detoxification in plants.[3][11][13]

Moreover, microbes could also potentially utilize nitrilase for detoxifying and assimilating nitriles and cyanide that exist in the plant environment.[11] An example of this is the β-cyano-L-alanine nitrilase by the plant bacterium P. fluorescens SBW25.[14] Although it is unknown whether this plant bacterium encounters toxic levels of β-cyano-ʟ-alanine in natural settings, nitrilase activity has been observed in cyanogenic plants; thus, it seems that the nitrilase serves as a predominant mechanism for detoxifying cyanide instead of β-cyano-ʟ-alanine.[11][14] Other bacterial applications of nitrilases produced by plant-associated microorganisms include the degradation of plant nitriles for a carbon and nitrogen source. P. fluorescens EBC191 hydrolyzes many arylacetonitriles, namely mandelonitrile, which serves as a defense against herbivores.[11][15][16]

• Winkler M, Glieder A, Klempier N (March 2006). "Enzyme stabilizer DTT catalyzes nitrilase analogue hydrolysis of nitriles". Chemical Communications (12): 1298–300. doi:10.1039/B516937B. PMID 16538253.

• nitrilase at the U.S. National Library of Medicine Medical Subject Headings (MeSH)