02902nas a2200301   4500008004100000022001400041245009800055210006900153260000900222300001100231490000800242520188100250653002502131653002402156653003702180653002702217653001802244653002602262100002502288700002502313700002302338700002302361700001802384700002302402700002202425700002702447856012602474       2024                        eng d  a0168-160500aGenome sequencing and protein modeling unraveled the 2AP biosynthesis in Bacillus cereus DB250 aGenome sequencing and protein modeling unraveled the 2AP biosynt  cMAR   a1106000 v4133 a<p>
	2-Acetyl-1-pyrroline (2AP) is an important and major flavor aroma compound responsible for the fragrance of basmati rice, cheese, wine, and several other food products. Biosynthesis of 2AP in aromatic rice and a few other plant species is associated with a recessive Betaine aldehyde dehydrogenase 2 (BADH2) gene. However, the literature is scant on the relationship between the functional BADH2 gene and 2AP biosynthesis in prokaryotic systems. Therefore, in the present study, we aimed to explore the functionality of the BADH2 gene for 2AP biosynthesis in 2AP synthesizing rice rhizobacterial isolate Bacillus cereus DB25 isolated from the rhizosphere of basmati rice (Oryza sativa L.). Full-length BcBADH2 sequence was obtained through whole genome sequencing (WGS) and further confirmed through traditional PCR and Sanger sequencing. Then the functionality of the BcBADH2 gene was evaluated in-silico through bioinformatics analysis and protein docking studies and further experimentally validated through enzyme assay. The sequencing and bioinformatics analysis results revealed a full-length 1485 bp BcBADH2 coding sequence without any deletion or premature stop codons. Full-length BcBADH2 was found to encode a fully functional protein of 54.08 kDa with pI of 5.22 and showed the presence of the conserved amino acids responsible for enzyme activity. The docking studies confirmed a good affinity between the protein and its substrate whereas the presence of BcBADH2 enzyme activity confirmed the functionality of BADH2 enzyme in B. cereus DB25. In conclusion, the findings of the present study suggest that B. cereus DB25 is able to synthesize 2AP despite a functional BADH2 gene and there may be a different molecular mechanism responsible for 2AP biosynthesis in bacterial systems, unlike that found in aromatic rice and other eukaryotic plant species.</p>
10a2-Acetyl-1-pyrroline10aBasmati rice flavor10aBetaine aldehyde dehydrogenase 210aProtein-ligand docking10aRhizobacteria10aWhole-genome sequence1 aDhondge, Harshal, V.1 aBarvkar, Vitthal, T.1 aDastager, Syed, G.1 aDharne, Mahesh, S.1 aRajput, Vinay1 aPable, Anupama, A.1 aHenry, Robert, J.1 aNadaf, Altafhusain, B.  uhttps://library.ncl.res.in/content/genome-sequencing-and-protein-modeling-unraveled-2ap-biosynthesis-bacillus-cereus-db25