<?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%">Maryono</style></author><author><style face="normal" font="default" size="100%">Netti Herawati</style></author><author><style face="normal" font="default" size="100%">Meuthia Aulia Farhani Gaffar</style></author><author><style face="normal" font="default" size="100%">Sartini</style></author><author><style face="normal" font="default" size="100%">Aliyah</style></author><author><style face="normal" font="default" size="100%">Elly Wahyudin</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Microwave-Assisted Extraction and Identification of γ- Oryzanol from Rice Bran (Oryza sativa L. cv Ciliwung)</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Microwave assisted extraction</style></keyword><keyword><style  face="normal" font="default" size="100%">Rice Bran (Oryza sativa L. cv Cilliwung)</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary metabolite</style></keyword><keyword><style  face="normal" font="default" size="100%">γ- Oryzanol</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">September 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">1242-1247</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;Rice Bran (&lt;em&gt;Oryza sativa&lt;/em&gt; L. cv Cilliwung) is a by-product of the rice milling process, consisting of an outer layer of rice grains with the whole seed institute. Rice bran oil is a result of rice bran extraction. Rice bran oil contains antioxidant compounds, one of which is oryzanol, so this study aims to determine the levels of or-oryzanol in rice bran. The stages of the research included sample preparation, extraction using Microwave-Assisted Extraction (MAE), followed by Vacuum Liquid Column Chromatography (VLCC) was extracted using the MAE method produced 30 mL of black-brown rice bran oil extract. A total of 8 grams of rice bran extract was obtained at VLCC using eluent (n-hexane: ethyl acetate) with ratios 9:1, 7:3, and 1:1, respectively. Then the five factions obtained were characterized using HPLC, and GC/MS identified the mass of the γ-oryzanol compound.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">5</style></issue><work-type><style face="normal" font="default" size="100%">Research Article</style></work-type><section><style face="normal" font="default" size="100%">1242</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Maryono&lt;sup&gt;1,&lt;/sup&gt;*, Netti Herawati&lt;sup&gt;1&lt;/sup&gt;, Meuthia Aulia Farhani Gaffar&lt;sup&gt;1&lt;/sup&gt;, Sartini&lt;sup&gt;2&lt;/sup&gt;, Aliyah&lt;sup&gt;2&lt;/sup&gt;, Elly Wahyudin&lt;sup&gt;2&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Chemistry, Faculty of Mathematics and Natural Sciences, Makassar State University, Makassar, South Sulawesi, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Faculty of Pharmacy, Hasanuddin University, Makassar, South Sulawesi, INDONESIA.&lt;/p&gt;
</style></auth-address></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%">Alfi Rumidatul</style></author><author><style face="normal" font="default" size="100%">Noor Rahmawati</style></author><author><style face="normal" font="default" size="100%">Sopandi Sunarya</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Production of Secondary Metabolites and its Antibacterial and Antioxidant Activity During the Growth Period of Endophytic Fungi Isolated from Gall Rust Sengon Plants</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacteri</style></keyword><keyword><style  face="normal" font="default" size="100%">Antioxidant</style></keyword><keyword><style  face="normal" font="default" size="100%">Endophytic fungi</style></keyword><keyword><style  face="normal" font="default" size="100%">Gall rust</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary metabolite</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2021</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">13</style></volume><pages><style face="normal" font="default" size="100%">325-331</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; In our previous study, secondary metabolites of endophytic fungi isolated from gall rust sengon showed their bioactive activity against antibacterial and antioxidant, but only gave little effect to antifungal activity. Endophytic fungal culture extracted from gall rust of sengon (&lt;em&gt;Falcataria moluccana&lt;/em&gt; Miq. Barneby and J. W. Grimes) has the ability on inhibiting&lt;em&gt; Bacillus subtilis, Pseudomonas aeruginosa&lt;/em&gt; and&lt;em&gt; Escherichia coli&lt;/em&gt;. To increase the production of bioactive compounds, this research was focused on isolates which produced the highest activity compounds, and sought the optimal fermentation conditions in the production of bioactive compounds. &lt;strong&gt;Methods:&lt;/strong&gt; The fermentation process was carried out on PDB liquid media for 21 days, under shaker conditions, at room temperature, and sampling measurements were hold every 3 days. Bioassay were carried out against &lt;em&gt;B. subtilis, P. aeruginosa&lt;/em&gt;, and &lt;em&gt;E. coli.&lt;/em&gt;&lt;strong&gt; Results:&lt;/strong&gt; The early stages fungal growth was adaptation stage, continued by 1-6&lt;sup&gt;th&lt;/sup&gt; days of exponential growth period. Day 6-12&lt;sup&gt;th&lt;/sup&gt; was stationary growth and day 15-21&lt;sup&gt;th&lt;/sup&gt; were cell death periode. The highest secondary metabolite production was achieved at stationary periodes, that was occured at days 9-15&lt;sup&gt;th&lt;/sup&gt;&amp;nbsp;and high antibacterial activity was produced on days 9-12&lt;sup&gt;th&lt;/sup&gt;. &lt;strong&gt;Conclusion: &lt;/strong&gt;The best production secondary metabolite that has high activity was at day 9-12&lt;sup&gt;th&lt;/sup&gt;.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">2</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">325</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Alfi Rumidatul&lt;sup&gt;1&lt;/sup&gt;, Noor Rahmawati&lt;sup&gt;1,&lt;/sup&gt;*, Sopandi Sunarya&lt;sup&gt;1&lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;School of Life Sciences and Technology, Institut Teknologi Bandung, Jalan Ganesha 10 Bandung 40132, West Java, INDONESIA.&lt;/p&gt;
</style></auth-address></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%">Andi Hamdillah</style></author><author><style face="normal" font="default" size="100%">Alim Isnansetyo</style></author><author><style face="normal" font="default" size="100%">Indah Istiqomah</style></author><author><style face="normal" font="default" size="100%">Indun Dewi Puspita</style></author><author><style face="normal" font="default" size="100%">Desy Putri Handayani</style></author><author><style face="normal" font="default" size="100%">Takushi Kaneko</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Antibacterial Activity of Coastal Plants and Marine Sponges from Kei Island Indonesia against Bacterial Fish Pathogens</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Antibacterial activity</style></keyword><keyword><style  face="normal" font="default" size="100%">Bacteria</style></keyword><keyword><style  face="normal" font="default" size="100%">Coastal plant</style></keyword><keyword><style  face="normal" font="default" size="100%">Fish pathogen</style></keyword><keyword><style  face="normal" font="default" size="100%">Marine sponge</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary metabolite</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">July 2019</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">11</style></volume><pages><style face="normal" font="default" size="100%">812-817</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; The objective of this study was to investigate the antibacterial activity of coastal plants and marine sponges extracts against fish bacterial pathogens. &lt;strong&gt;Methods:&lt;/strong&gt; Samples were extracted by maceration and the extracts were examined for their antibacterial activities against &lt;em&gt;Streptococcus&lt;/em&gt; sp. BJ0509, &lt;em&gt;Staphylococcus aureus&lt;/em&gt; ATCC 6538,&lt;em&gt; Aeromonas hydrophila&lt;/em&gt; BA03 and &lt;em&gt;Vibrio parahaemolyticus&lt;/em&gt; 29S by means of paper disc diffusion method. Active extracts were partitioned and purified by column chromatography. The purified substance was tested for Minimum Inhibitory Concentration (MIC) against seven bacterial fish pathogens namely&lt;em&gt; Streptococcus &lt;/em&gt;sp., &lt;em&gt;Vibrio parahaemolyticus&lt;/em&gt;, &lt;em&gt;V. alginolyticus, V. harveyi, Photobacterium damselae, Aeromonas hydrophila and A. dhakensis.&lt;/em&gt; &lt;strong&gt;Results: &lt;/strong&gt;The highest antibacterial activity against all bacteria used in the assay was demonstrated by OKA 6, a bark extract sample of a coastal plant, &lt;em&gt;Diospyros maritima.&lt;/em&gt; It showed a diameter of inhibition zones against &lt;em&gt;Streptococcus &lt;/em&gt;sp. BJ0509, &lt;em&gt;S. aureus&lt;/em&gt; ATCC 6538, &lt;em&gt;A. hydrophila&lt;/em&gt; BA03 and &lt;em&gt;V. parahaemolyticus&lt;/em&gt; 29S of 19, 33, 18, and 18 mm, respectively. The column chromatography fraction of OKA 6 inhibited the growth of &lt;em&gt;S. aureus&lt;/em&gt; ATCC 6538 with MIC of 3.125 μg/mL. The MIC of this fraction against seven bacterial fish pathogens ranged &amp;lt; 0.098 to 3.125 μg/mL. The antibacterial activity of partially purified substance obtained from column chromatography fractionation of OKA 6 was higher than those of oxytetracycline and kanamycin. &lt;strong&gt;Conclusions: &lt;/strong&gt;This result indicates that antibacterial activity of the partially purified substance is potentially higher than those of the commercial antibiotics tested. It further indicates that OKA 6 extract from &lt;em&gt;D. maritima&lt;/em&gt; can serve as a promising resource for the development of therapeutic agents against bacterial infections in aquaculture.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">4</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">812</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p class=&quot;rtejustify&quot;&gt;&lt;strong&gt;Andi Hamdillah&lt;sup&gt;1&lt;/sup&gt;, Alim Isnansetyo&lt;sup&gt;1,*&lt;/sup&gt;, Indah Istiqomah&lt;sup&gt;1&lt;/sup&gt;, Indun Dewi Puspita&lt;sup&gt;1&lt;/sup&gt;, Desy Putri Handayani&lt;sup&gt;1&lt;/sup&gt;, Takushi Kaneko&lt;sup&gt;2&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;1&lt;/sup&gt;Department of Fisheries, Faculty of Agriculture, Universitas Gadjah Mada, Jl. Flora, Bulaksumur, Yogyakarta, INDONESIA.&lt;/p&gt;

&lt;p class=&quot;rtejustify&quot;&gt;&lt;sup&gt;2&lt;/sup&gt;Global Alliance for TB Drug Development, Research and Development, 40 Wall Street, 24&lt;sup&gt;th&lt;/sup&gt; Floor, New York, NY, USA.&lt;/p&gt;
</style></auth-address></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%">Haviah Hafidhotul Ilmiah</style></author><author><style face="normal" font="default" size="100%">Tri Rini Nuringtyas</style></author><author><style face="normal" font="default" size="100%">Laurentius Hartanto Nugroho</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Accumulation of Potential Photo-Protective Compound Groups in Mangrove (Sonneratia caseolaris (l.) Engler.) Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Leaf anatomy.</style></keyword><keyword><style  face="normal" font="default" size="100%">Photo-protective</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary metabolite</style></keyword><keyword><style  face="normal" font="default" size="100%">Sonneratia caseolaris (L.) Engler</style></keyword><keyword><style  face="normal" font="default" size="100%">SPF</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">x</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">XX-XX</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; To analyze the accumulation of potential photo-protective compound groups, include phenol, flavonoid, and tannin in the leaf tissues of &lt;em&gt;Sonneratia caseolaris&lt;/em&gt; (L.) Engler. &lt;strong&gt;Methods:&lt;/strong&gt; The research used &lt;em&gt;Sonneratia caseolaris&lt;/em&gt; (L.) Engler leaves as materials. The total of compound groups and photo-protective ability level of each tissue was measured using spectrophotometry, while detection of compound group accumulations in the leaf tissue were observed using histochemical assay. &lt;strong&gt;Results:&lt;/strong&gt; Epidermis extract contained the highest content of total phenolic compounds (phenol, flavonoid, and tannin), followed by those of mesophyll and whole leaf. Moreover, Sun Protection Factor (SPF) value of epidermis was also higher than those of mesophyll and whole leaf, considering that there were no significant difference of SPF value between mesophyll and whole leaf. Result of histochemical assay of &lt;em&gt;S. caseolaris&lt;/em&gt; fresh leaf sections showed that phenol, flavonoid, and tannin were highly accumulated in the epidermis and some parts of mesophyll. &lt;strong&gt;Conclusion:&lt;/strong&gt; Potential photo-protective compound groups of &lt;em&gt;S. caseolaris&lt;/em&gt; leaves were accumulated in epidermis and mesophyll. However, epidermis showed the highest level of potential photo-protective compound groups than those of other tissues. Photo-protective ability of epidermis also showed higher value than those of mesophyll.&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Key words:&lt;/strong&gt; &lt;em&gt;Sonneratia caseolaris&lt;/em&gt; (L.) Engler, Secondary metabolite, Photo-protective, SPF, Leaf anatomy.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">2s</style></issue><work-type><style face="normal" font="default" size="100%">x</style></work-type><section><style face="normal" font="default" size="100%">x</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Haviah Hafidhotul Ilmiah, Tri Rini Nuringtyas, Laurentius Hartanto Nugroho&lt;sup&gt;* &lt;/sup&gt;&lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Faculty of Biology, Universitas Gadjah Mada, Jalan Teknika Selatan, Sekip Utara, Yogyakarta, 55281, INDONESIA.&lt;/p&gt;</style></auth-address></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%">Haviah Hafidhotul Ilmiah</style></author><author><style face="normal" font="default" size="100%">Tri Rini Nuringtyas</style></author><author><style face="normal" font="default" size="100%">Laurentius Hartanto Nugroho</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Accumulation of Potential Photo-Protective Compound Groups in Mangrove (Sonneratia caseolaris (L.) Engler.) Leaves</style></title><secondary-title><style face="normal" font="default" size="100%">Pharmacognosy Journal</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Leaf anatomy</style></keyword><keyword><style  face="normal" font="default" size="100%">Photo-protective</style></keyword><keyword><style  face="normal" font="default" size="100%">Secondary metabolite</style></keyword><keyword><style  face="normal" font="default" size="100%">Sonneratia caseolaris (L.) Engler</style></keyword><keyword><style  face="normal" font="default" size="100%">SPF</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2018</style></year><pub-dates><date><style  face="normal" font="default" size="100%">March 2018</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">http://fulltxt.org/article/527</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">10</style></volume><pages><style face="normal" font="default" size="100%">576-580</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Objective:&lt;/strong&gt; To analyze the accumulation of potential photo-protective compound groups, include phenol, flavonoid, and tannin in the leaf tissues of &lt;em&gt;Sonneratia caseolaris&lt;/em&gt; (L.) Engler. &lt;strong&gt;Methods:&lt;/strong&gt; The research used &lt;em&gt;Sonneratia caseolaris&lt;/em&gt; (L.) Engler leaves as materials. The total of compound groups and photo-protective ability level of each tissue was measured using spectrophotometry, while detection of compound group accumulations in the leaf tissue were observed using histochemical assay. &lt;strong&gt;Results:&lt;/strong&gt; Epidermis extract contained the highest content of total phenolic compounds (phenol, flavonoid, and tannin), followed by those of mesophyll and whole leaf. Moreover, Sun Protection Factor (SPF) value of epidermis was also higher than those of mesophyll and whole leaf, considering that there were no significant difference of SPF value between mesophyll and whole leaf. Result of histochemical assay of &lt;em&gt;S. caseolaris&lt;/em&gt; fresh leaf sections showed that phenol, flavonoid, and tannin were highly accumulated in the epidermis and some parts of mesophyll. &lt;strong&gt;Conclusion:&lt;/strong&gt; Potential photo-protective compound groups of &lt;em&gt;S. caseolaris&lt;/em&gt; leaves were accumulated in epidermis and mesophyll. However, epidermis showed the highest level of potential photo-protective compound groups than those of other tissues. Photo-protective ability of epidermis also showed higher value than those of mesophyll.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">3</style></issue><work-type><style face="normal" font="default" size="100%">Original Article</style></work-type><section><style face="normal" font="default" size="100%">576</style></section><auth-address><style face="normal" font="default" size="100%">&lt;p style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;Haviah Hafidhotul Ilmiah, Tri Rini Nuringtyas, Laurentius Hartanto Nugroho&lt;sup&gt;*&lt;/sup&gt; &lt;/strong&gt;&lt;/p&gt;
&lt;p style=&quot;text-align: justify;&quot;&gt;Faculty of Biology, Universitas Gadjah Mada, Jalan Teknika Selatan, Sekip Utara, Yogyakarta, 55281, INDONESIA.&lt;/p&gt;</style></auth-address></record></records></xml>