<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Giri, Pritam</style></author><author><style face="normal" font="default" size="100%">Lim, Seonga</style></author><author><style face="normal" font="default" size="100%">Khobragade, Taresh P.</style></author><author><style face="normal" font="default" size="100%">Pagar, Amol D.</style></author><author><style face="normal" font="default" size="100%">Patil, Mahesh D.</style></author><author><style face="normal" font="default" size="100%">Sarak, Sharad</style></author><author><style face="normal" font="default" size="100%">Jeon, Hyunwoo</style></author><author><style face="normal" font="default" size="100%">Joo, Sangwoo</style></author><author><style face="normal" font="default" size="100%">Goh, Younghwan</style></author><author><style face="normal" font="default" size="100%">Jung, Seohee</style></author><author><style face="normal" font="default" size="100%">Jang, Yu-Jeong</style></author><author><style face="normal" font="default" size="100%">Choi, Seung Beom</style></author><author><style face="normal" font="default" size="100%">Kim, Ye Chan</style></author><author><style face="normal" font="default" size="100%">Kang, Taek Jin</style></author><author><style face="normal" font="default" size="100%">Heo, Yong-Seok</style></author><author><style face="normal" font="default" size="100%">Yun, Hyungdon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Biocatalysis enables the scalable conversion of biobased furans into various furfurylamines</style></title><secondary-title><style face="normal" font="default" size="100%">NATURE COMMUNICATIONS</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Biomass</style></keyword><keyword><style  face="normal" font="default" size="100%">OMEGA-TRANSAMINASE</style></keyword><keyword><style  face="normal" font="default" size="100%">OXIDASE</style></keyword><keyword><style  face="normal" font="default" size="100%">Reductive amination</style></keyword><keyword><style  face="normal" font="default" size="100%">SPECIFICITY</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JUL </style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">15</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">1</style></issue><work-type><style face="normal" font="default" size="100%">Journal Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;
&lt;h3 class=&quot;label colonMark ng-star-inserted&quot; data-ta=&quot;FRkeywordsTa-keyWordsPlusLabel&quot; dir=&quot;auto&quot; id=&quot;FRkeywordsTa-keyWordsPlusLabel&quot;&gt;
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&lt;p&gt;&amp;nbsp;&lt;/p&gt;
&lt;p&gt;&amp;nbsp;&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;16.6&lt;/p&gt;
</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Paul, Shatabdi</style></author><author><style face="normal" font="default" size="100%">Yadav, Binduma</style></author><author><style face="normal" font="default" size="100%">Patil, Mahesh D.</style></author><author><style face="normal" font="default" size="100%">Pujari, Anil Kumar</style></author><author><style face="normal" font="default" size="100%">Singh, Umesh</style></author><author><style face="normal" font="default" size="100%">Rishi, Vikas</style></author><author><style face="normal" font="default" size="100%">Bhaumik, Jayeeta</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">photoarchitectonic hydrogel for synergistic in vitro chemo–phototherapy of breast cancer</style></title><secondary-title><style face="normal" font="default" size="100%">Materials Advances</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2024</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JAN</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">1903-1916</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	&lt;span style=&quot;color: rgba(0, 0, 0, 0.79); font-family: &amp;quot;Source Sans Pro&amp;quot;, source-sans-pro, museo_sans300, museo-sans, Arial, sans-serif; font-size: 16px;&quot;&gt;Currently, combinatorial therapy has evoked interest in cancer treatment, and may promote achieving a synergistic effect using cancer medicines. Laser-assisted and pH-responsive therapies have attracted significant attention, and their combination leads to high efficiency cancer treatment. Herein, we developed a chemo–phototherapeutic hydrogel comprised of doxorubicin (DOX, a chemotherapeutic drug) and zinc phthalocyanine (ZnPc, a phototherapeutic drug) for combinatorial and synergistic treatment of breast cancer. Firstly, we have developed carbon dots (CDs, size of ∼5 nm) utilizing lignin and folic acid as biocompatible sources. Then doxorubicin was loaded on the surface of the carbon dots&amp;nbsp;&lt;/span&gt;&lt;em style=&quot;color: rgba(0, 0, 0, 0.79); font-family: &amp;quot;Source Sans Pro&amp;quot;, source-sans-pro, museo_sans300, museo-sans, Arial, sans-serif; font-size: 16px;&quot;&gt;via&lt;/em&gt;&lt;span style=&quot;color: rgba(0, 0, 0, 0.79); font-family: &amp;quot;Source Sans Pro&amp;quot;, source-sans-pro, museo_sans300, museo-sans, Arial, sans-serif; font-size: 16px;&quot;&gt;&amp;nbsp;conjugation (DOX@CDs). Later on, zinc phthalocyanine and acrylic acid derivatives were utilized to develop a laser-responsive hydrogel (ZnPc-PP H). Afterward, doxorubicin-conjugated carbon dots were incorporated into the photoarchitectonic hydrogel to develop a chemo–phototherapeutic drug-loaded hydrogel (DOX@CDs–ZnPc-PP H). Subsequently, the&amp;nbsp;&lt;/span&gt;&lt;em style=&quot;color: rgba(0, 0, 0, 0.79); font-family: &amp;quot;Source Sans Pro&amp;quot;, source-sans-pro, museo_sans300, museo-sans, Arial, sans-serif; font-size: 16px;&quot;&gt;in vitro&lt;/em&gt;&lt;span style=&quot;color: rgba(0, 0, 0, 0.79); font-family: &amp;quot;Source Sans Pro&amp;quot;, source-sans-pro, museo_sans300, museo-sans, Arial, sans-serif; font-size: 16px;&quot;&gt;&amp;nbsp;pH-triggering experiments demonstrated that the hydrogel loaded with both DOX and ZnPc could release the drugs in an acidic environment. Interestingly,&amp;nbsp;&lt;/span&gt;&lt;em style=&quot;color: rgba(0, 0, 0, 0.79); font-family: &amp;quot;Source Sans Pro&amp;quot;, source-sans-pro, museo_sans300, museo-sans, Arial, sans-serif; font-size: 16px;&quot;&gt;in vitro&lt;/em&gt;&lt;span style=&quot;color: rgba(0, 0, 0, 0.79); font-family: &amp;quot;Source Sans Pro&amp;quot;, source-sans-pro, museo_sans300, museo-sans, Arial, sans-serif; font-size: 16px;&quot;&gt;&amp;nbsp;assays confirmed that DOX@CDs–ZnPc-PP H could effectively target breast cancer cells (MCF-7). Furthermore, the developed chemo–phototherapeutic hydrogel exhibited non-cytotoxic behavior. Owing to laser assisted reactive oxygen species generation from ZnPc present in the hydrogel, the growth of MCF-7 cells was significantly lowered. In conclusion, all experimental outcomes indicate that the photoarchitectonic hydrogel has the potential to be applied in synergistic chemo- and photodynamic therapy of cancer.&lt;/span&gt;&lt;/p&gt;
</style></abstract><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;
	Foreign&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	5.2&lt;/p&gt;
</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Mohne, Devesh</style></author><author><style face="normal" font="default" size="100%">Reddy, Yeddula Nikhileshwar</style></author><author><style face="normal" font="default" size="100%">Rawat, Kshitij</style></author><author><style face="normal" font="default" size="100%">Patil, Mahesh D.</style></author><author><style face="normal" font="default" size="100%">Bhaumik, Jayeeta</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Immobilization of aldehyde reductase for the production of bioplastic precursors from agricultural fatty acids</style></title><secondary-title><style face="normal" font="default" size="100%">RSC Sustainability</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JUL</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">3</style></volume><pages><style face="normal" font="default" size="100%">3910-3914</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;div class=&quot;abstract author&quot; id=&quot;aep-abstract-id6&quot; style=&quot;box-sizing: border-box; margin: 0px 0px 8px; padding: 0px; color: rgb(31, 31, 31); font-family: ElsevierGulliver, Georgia, &amp;quot;Times New Roman&amp;quot;, Times, STIXGeneral, &amp;quot;Cambria Math&amp;quot;, &amp;quot;Lucida Sans Unicode&amp;quot;, &amp;quot;Microsoft Sans Serif&amp;quot;, &amp;quot;Segoe UI Symbol&amp;quot;, &amp;quot;Arial Unicode MS&amp;quot;, serif, sans-serif; font-size: 16px;&quot;&gt;
	&lt;div id=&quot;aep-abstract-sec-id7&quot; style=&quot;box-sizing: border-box; margin: 0px; padding: 0px;&quot;&gt;
		&lt;div class=&quot;u-margin-s-bottom&quot; style=&quot;box-sizing: border-box; margin-top: 0px; margin-right: 0px; margin-bottom: 16px !important; margin-left: 0px; padding: 0px;&quot;&gt;
			Herein, we report the biosynthesis of bioplastic precursors thourgh the immobilization of aldehyde reductase (AHR) onto a metal organic framework (UIO-66-NH&lt;span style=&quot;box-sizing: border-box; margin: 0px; padding: 0px; font-size: 12px; line-height: 0; position: relative; vertical-align: baseline; bottom: -0.25em;&quot;&gt;2&lt;/span&gt;). Kinetic analysis demonstrated that the immobilized AHR maintained significant catalytic activity and exhibited improved operational stability, as well as higher reusability, compared with the free AHR. Furthermore, the synthetic applicability of the immobilized AHR was evaluated in tandem with that of transaminase derived from&amp;nbsp;&lt;em style=&quot;box-sizing: border-box; margin: 0px; padding: 0px;&quot;&gt;S. pomeroyi&lt;/em&gt;&amp;nbsp;(spTA), where 8, 10, and 12 carbon chain ω-amino fatty acids (ω-AFAs) were biosynthesized from the corresponding hydroxy fatty acids (ω-HFAs) with ∼90% conversions.&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;div class=&quot;abstract graphical&quot; id=&quot;aep-abstract-id8&quot; style=&quot;box-sizing: border-box; margin: 0px 0px 8px; padding: 0px; color: rgb(31, 31, 31); font-family: ElsevierGulliver, Georgia, &amp;quot;Times New Roman&amp;quot;, Times, STIXGeneral, &amp;quot;Cambria Math&amp;quot;, &amp;quot;Lucida Sans Unicode&amp;quot;, &amp;quot;Microsoft Sans Serif&amp;quot;, &amp;quot;Segoe UI Symbol&amp;quot;, &amp;quot;Arial Unicode MS&amp;quot;, serif, sans-serif; font-size: 16px;&quot;&gt;
	&lt;div id=&quot;aep-abstract-sec-id9&quot; style=&quot;box-sizing: border-box; margin: 0px; padding: 0px;&quot;&gt;
		&lt;div class=&quot;u-margin-s-bottom&quot; style=&quot;box-sizing: border-box; margin-top: 0px; margin-right: 0px; margin-bottom: 16px !important; margin-left: 0px; padding: 0px;&quot;&gt;
			Herein, we report the biosynthesis of bioplastic precursors&amp;nbsp;&lt;em style=&quot;box-sizing: border-box; margin: 0px; padding: 0px;&quot;&gt;via&lt;/em&gt;&amp;nbsp;the immobilization of aldehyde reductase (AHR) onto a metal organic framework (UIO-66-NH&lt;span style=&quot;box-sizing: border-box; margin: 0px; padding: 0px; font-size: 12px; line-height: 0; position: relative; vertical-align: baseline; bottom: -0.25em;&quot;&gt;2&lt;/span&gt;).&lt;/div&gt;
	&lt;/div&gt;
&lt;/div&gt;
&lt;p&gt;
	&amp;nbsp;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">9</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;
	Foreign&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	4.9&lt;/p&gt;
</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Khobragade, Taresh P.</style></author><author><style face="normal" font="default" size="100%">Giri, Pritam</style></author><author><style face="normal" font="default" size="100%">Patil, Mahesh D.</style></author><author><style face="normal" font="default" size="100%">Joo, Sangwoo</style></author><author><style face="normal" font="default" size="100%">Cho, Sunga</style></author><author><style face="normal" font="default" size="100%">Kim, Yechan</style></author><author><style face="normal" font="default" size="100%">Ghosh, Rohan</style></author><author><style face="normal" font="default" size="100%">Jeong, Sanghun</style></author><author><style face="normal" font="default" size="100%">Maeng, Minyeong</style></author><author><style face="normal" font="default" size="100%">Song, Min-Ho</style></author><author><style face="normal" font="default" size="100%">Park, Jeong-Min</style></author><author><style face="normal" font="default" size="100%">Lee, Eun Ho</style></author><author><style face="normal" font="default" size="100%">Keum, Young-Soo</style></author><author><style face="normal" font="default" size="100%">Kang, Taek Jin</style></author><author><style face="normal" font="default" size="100%">Heo, Yong-Seok</style></author><author><style face="normal" font="default" size="100%">Yun, Hyungdon</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Total biocatalytic synthesis of capsaicinoids using ferulic acid: a versatile two-step strategy for natural product diversification</style></title><secondary-title><style face="normal" font="default" size="100%">Angewandte Chemie-International Edition</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Capsaicinoids</style></keyword><keyword><style  face="normal" font="default" size="100%">Carboxylic acid reductase</style></keyword><keyword><style  face="normal" font="default" size="100%">Transaminase</style></keyword><keyword><style  face="normal" font="default" size="100%">Vanillylamine</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">DEC </style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">64</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	The wide-ranging application of capsaicinoids, the active compounds in chili peppers, has driven increasing interest in the development of sustainable production strategies. However, capsaicinoid synthesis remains a challenge. The objective of this pioneering study is to report the total biocatalytic synthesis of structurally diverse capsaicinoids from bio-based ferulic acids. An X-ray crystallographic study elucidated the structural basis for the exceptional potential of a novel transaminase from Phaeobacter porticola (PPTA) to transform the highest ever reported concentration of vanillin (100-200 mM) to vanillylamine, with &amp;gt;99% conversion and modest conversion ranging from 48% to 79% for 300 to 500 mM substrate. Using PPTA in tandem with phenolic acid decarboxylase (PAD) and aromatic dioxygenase (ADO) further enabled the direct synthesis of vanillylamine from ferulic acid with &amp;gt;99% conversion. Furthermore, the integration of a multi-enzymatic cascade with carboxylic acid reductases (CARs) successfully synthesized structurally diverse capsaicinoids via amide bond formation between vanillylamine and free fatty acids, with excellent conversions ranging from 72% to &amp;gt;88%. A 50-mM enzymatic reaction afforded 95% and 80% conversion of vanillylamine and capsaicin, respectively.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">49</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	17&lt;/p&gt;
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