01985nas a2200277   4500008004100000022001400041245011000055210006900165260007400234300001200308490000800320520103100328653001601359653001101375653001301386653002401399653001401423653001701437100002701454700002401481700002001505700002501525700002001550700001701570856012001587       2007                        eng d  a1520-610600aNCL-7, a novel all silica analog of polymorph B rich member of BEA family: synthesis and characterization0 aNCL7 a novel all silica analog of polymorph B rich member of BEA  a1155 16TH ST, NW, WASHINGTON, DC 20036 USAbJapan Assoc ZeolitescAPR  a108-1140 v1013 a<p>{Polymorph B-rich BEA type structure, NCL-7, was synthesized using hydrothermal method in fluoride medium using perchloric acid as promoter. The samples were characterized using XRD, low temperature N-2-adsorption and Si-29 MASNMR. As the structure of beta is highly disordered Rietveld refinement of powder XRD patterns is precluded. Phase composition is derived using the simulated patterns for the random intergrowths of polymorph A and B by DIFFaX. The stacking direction c' is perpendicular to the a'b' plane of the layer. The composition of polymorph B is found to be ca. 60-65%. Two other structures namely NCL-5 and NCL-6 with varying degree of polymorph B enrichment were also synthesized. Synthesis parameters such as effect of H2O/SiO2, TEAOH/SiO2, HClO4/SiO2 and crystallization temperature were studied thoroughly. The present article explains for the first time the synthesis and characterization of NCL-7, an analog of BEA type family with enrichment of polymorph B and its comparison with normal beta (*</p>10aB-polymorph10aDIFFaX10aPromoter10aReitveld refinement10asynthesis10azeolite beta1 aKadgaonkar, Mahesh, D.1 aKasture, Mahesh, W.1 aBhange, Deu, S.1 aJoshi, Praphulla, N.1 aRamaswamy, Veda1 aKumar, Rajiv  uhttps://library.ncl.res.in/content/ncl-7-novel-all-silica-analog-polymorph-b-rich-member-bea-family-synthesis-and-000820nas a2200217   4500008004100000022001400041245008900055210006900144260007300213300001400286490000600300520003200306653001800338653002600356653001200382653001300394100002300407700002500430700002900455856011800484       2007                        eng d  a1566-736700aTethered Pd-complex on solid support: catalyst for acid-free carbonylation reactions0 aTethered Pdcomplex on solid support catalyst for acidfree carbon  aPO BOX 211, 1000 AE AMSTERDAM, NETHERLANDSbELSEVIER SCIENCE BVcSEP  a1386-13920 v83 a<p>{Palladium complex [</p>10adecomposition10adirect H2O2 synthesis10ahalides10aPromoter1 aSarkar, Bibbas, R.1 aMukhopadhyay, Kausik1 aChaudhari, Raghunath, V.  uhttps://library.ncl.res.in/content/tethered-pd-complex-solid-support-catalyst-acid-free-carbonylation-reactions-002856nas a2200277   4500008004100000022001400041245009000055210006900145260005700214300001200271490000800283520193300291653001002224653001302234653002202247653001302269653002502282100002202307700002002329700002802349700002202377700001902399700002102418700002002439856011902459       2015                        eng d  a0032-093500aStructural features of diverse Pin-II proteinase inhibitor genes from capsicum annuum0 aStructural features of diverse PinII proteinase inhibitor genes   a233 SPRING ST, NEW YORK, NY 10013 USAbSPRINGERcFEB  a319-3310 v2413 a<p>The proteinase inhibitor (PI) genes from Capsicum annuum were characterized with respect to their UTR, introns and promoter elements. The occurrence of PIs with circularly permuted domain organization was evident. Several potato inhibitor II (Pin-II) type proteinase inhibitor (PI) genes have been analyzed from Capsicum annuum (L.) with respect to their differential expression during plant defense response. However, complete gene characterization of any of these C. annuum PIs (CanPIs) has not been carried out so far. Complete gene architectures of a previously identified CanPI-7 (Beads-on-string, Type A) and a member of newly isolated Bracelet type B, CanPI-69 are reported in this study. The 5' UTR (untranslated region), 3'UTR, and intronic sequences of both the CanPI genes were obtained. The genomic sequence of CanPI-7 exhibited, exon 1 (49 base pair, bp) and exon 2 (740 bp) interrupted by a 294-bp long type I intron. We noted the occurrence of three multi-domain PIs (CanPI-69, 70, 71) with circularly permuted domain organization. CanPI-69 was found to possess exon 1 (49 bp), exon 2 (551 bp) and a 584-bp long type I intron. The upstream sequence analysis of CanPI-7 and CanPI-69 predicted various transcription factor-binding sites including TATA and CAAT boxes, hormone-responsive elements (ABRELATERD1, DOFCOREZM, ERELEE4), and a defense-responsive element (WRKY71OS). Binding of transcription factors such as zinc finger motif MADS-box and MYB to the promoter regions was confirmed using electrophoretic mobility shift assay followed by mass spectrometric identification. The 3' UTR analysis for 25 CanPI genes revealed unique/distinct 3' UTR sequence for each gene. Structures of three domain CanPIs of type A and B were predicted and further analyzed for their attributes. This investigation of CanPI gene architecture will enable the better understanding of the genetic elements present in CanPIs.</p>10aCanPI10aCapsicum10aGene architecture10aPromoter10aProteinase inhibitor1 aMahajan, Neha, S.1 aDewangan, Veena1 aLomate, Purushottam, R.1 aJoshi, Rakesh, S.1 aMishra, Manasi1 aGupta, Vidya, S.1 aGiri, Ashok, P.  uhttps://library.ncl.res.in/content/structural-features-diverse-pin-ii-proteinase-inhibitor-genes-capsicum-annuum-0