@article { ISI:000244304100004,
	title = {Nuclease Stn alpha from Streptomyces thermonitrificans: characterization of the associated adenylic acid preferential ribonuclease activity},
	journal = {Current Microbiology},
	volume = {54},
	number = {3},
	year = {2007},
	month = {MAR},
	pages = {186-189},
	publisher = {SPRINGER},
	type = {Article},
	address = {233 SPRING STREET, NEW YORK, NY 10013 USA},
	abstract = {<p>Nuclease Stn alpha from Streptomyces thermonitrificans hydrolyses DNA and RNA at the rate of approximately 10:l. The optimum pH and temperature for RNA hydrolysis were 7.0 and 45 degrees C. The RNase activity of nuclease Stn alpha had neither an obligate requirement of metal ions nor was it activated in the presence of metal ions. The enzyme was inhibited by Zn2+, Mg2+, Co2+, and Ca2+; inorganic phosphate; pyrophosphate; NaCl; KCl; and metal chelators. It was stable at high concentrations of urea but susceptible to low concentrations of Sodium dodecyl sulfate and guanidine hydrochloride. The rates by which nuclease Stn alpha hydrolysed polyribonucleotides occurs in the order of poly A \&gt;\&gt; RNA \&gt;\&gt; poly U \&gt; poly G \&gt; poly C. The enzyme cleaved RNA to 3{\textquoteright} mononucleotides with preferential liberation of 3{\textquoteright}AMP, indicating it to be an adenylic acid preferential endonuclease.</p>},
	issn = {0343-8651},
	doi = {10.1007/s00284-006-0020-y},
	author = {Deshmukh, Satej S.}
}
@article {46112,
	title = {Neutral imino-methyl benzenesulfonate-ligated Pd(II) complexes and implications in ethylene polymerization},
	journal = {ACS Omega},
	volume = {4},
	year = {2019},
	month = {MAY},
	pages = {9502-9511},
	type = {Article},
	abstract = {<p>A reaction between sodium 2-formylbenzenesulfonate and aniline revealed the near-quantitative (91\%) formation of sodium-2-((phenylimino)methyl)benzenesulfonate L1. The identity of L1 was unambiguously ascertained using spectroscopic and analytical methods. The scope of this methodology was widened and various electron-donating amines were treated with sodium 2-formylbenzenesulfonate, and a small library of 6 imine ligands L2-L6 was generated. When L2 was treated with [(COD)PdMeCI], instead of the anticipated [L2PdMe(DMSO)] complex, the formation of [(DMSO)(2)Pd2Cl2Me2] Pd Dim was observed. Nevertheless, the desired imino-methyl benzenesulfonate-ligated palladium complex [L2PdMe(Lu)] C1 was obtained by in situ abstraction of chloride and addition of bulky 2,6-lutidine as the donor group. The observation of characteristic Pd-Me protons at 0.06 ppm and the corresponding carbon at -8.1 ppm indicated the formation of C1. These 1D NMR observations were corroborated by 2D C-H correlation spectra and mass analysis, and the existence of C1 was unambiguously ascertained. Along the same lines, L4 and L5 were treated with a palladium precursor to produce [L4/SPdMe(Lu)]-type complexes C2-C3 in 55-84\% yield, and their identity was established by using a combination of spectroscopic tools, analytical methods, and single-crystal X-ray diffraction. The synthetic utility of C1-C3 has been demonstrated by utilizing these complexes in the insertion polymerization of ethylene to polyethylene.</p>
},
	issn = {2470-1343},
	doi = {10.1021/acsomega.9b00709},
	author = {Deshmukh, Satej S. and Gaikwad, Shahaji R. and Mote, Nilesh R. and Manod, M. and Gonnade, Rajesh G. and Chikkali, Samir H.}
}
