• Title/Summary/Keyword: environmental biotechnology

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Wood Decay Fungi in South Korea: Polypores from Seoul

  • Jang, Yeongseon;Jang, Seokyoon;Lee, Jaejung;Lee, Hwanhwi;Lee, Hanbyul;Lee, Young Min;Hong, Joo-Hyun;Min, Mihee;Lim, Young Woon;Kim, Changmu;Kim, Jae-Jin
    • Mycobiology
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    • v.42 no.2
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    • pp.140-146
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    • 2014
  • In Seoul, a majority of plant communities have undergone significant changes over the last few decades; however, how wood decay fungi have responded and adapted to the changes in vegetation remains unknown. Through an ongoing investigation of Korean indigenous fungi, ca. 300 specimens with poroid basidiocarp were collected in Seoul during 2008~2012. Morphological examination and molecular analysis using the internal transcribed spacer and nuclear large subunit ribosomal DNA region sequences helped identify 38 species belonging to 28 genera, 10 families, and 5 orders in this area. Among them, three polypores, Abundisporus pubertatis, Coriolopsis strumosa, and Perenniporia maackiae were found to be new to South Korea.

Isolation and Characterization of a Novel Calcium/Calmodulin-Dependent Protein Kinase, AtCK, from Arabidopsis

  • Jeong, Jae Cheol;Shin, Dongjin;Lee, Jiyoung;Kang, Chang Ho;Baek, Dongwon;Cho, Moo Je;Kim, Min Chul;Yun, Dae-Jin
    • Molecules and Cells
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    • v.24 no.2
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    • pp.276-282
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    • 2007
  • Protein phosphorylation is one of the major mechanisms by which eukaryotic cells transduce extracellular signals into intracellular responses. Calcium/calmodulin ($Ca^{2+}/CaM$)-dependent protein phosphorylation has been implicated in various cellular processes, yet little is known about $Ca^{2+}/CaM$-dependent protein kinases (CaMKs) in plants. From an Arabidopsis expression library screen using a horseradish peroxidase-conjugated soybean calmodulin isoform (SCaM-1) as a probe, we isolated a full-length cDNA clone that encodes AtCK (Arabidopsis thaliana calcium/calmodulin-dependent protein kinase). The predicted structure of AtCK contains a serine/threonine protein kinase catalytic domain followed by a putative calmodulin-binding domain and a putative $Ca^{2+}$-binding domain. Recombinant AtCK was expressed in E. coli and bound to calmodulin in a $Ca^{2+}$-dependent manner. The ability of CaM to bind to AtCK was confirmed by gel mobility shift and competition assays. AtCK exhibited its highest levels of autophosphorylation in the presence of 3 mM $Mn^{2+}$. The phosphorylation of myelin basic protein (MBP) by AtCK was enhanced when AtCK was under the control of calcium-bound CaM, as previously observed for other $Ca^{2+}/CaM$-dependent protein kinases. In contrast to maize and tobacco CCaMKs (calcium and $Ca^{2+}/CaM$-dependent protein kinase), increasing the concentration of calmodulin to more than $3{\mu}M$ suppressed the phosphorylation activity of AtCK. Taken together our results indicate that AtCK is a novel Arabidopsis $Ca^{2+}/CaM$-dependent protein kinase which is presumably involved in CaM-mediated signaling.

An Efficient and Convenient Esterification of Carboxylic Acids Using 4,5-Dichloro-2-[(4-nitrophenyl)sulfonyl]pyridazin-3(2H)-one

  • Kim, Jeum-Jong;Park, Yong-Dae;Kweon, Deok-Heon;Kang, Young-Jin;Kim, Ho-Kyun;Lee, Sang-Gyeong;Cho, Su-Dong;Lee, Woo-Song;Yoon, Yong-Jin
    • Bulletin of the Korean Chemical Society
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    • v.25 no.4
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    • pp.501-505
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    • 2004
  • Esterification of aliphatic or aromatic carboxylic acids with alcohols using 2-(4-nitrobenzenesulfonyl)-4,5-dichloropyridazin-3(2H)-one (3) in the presence of base in organic solvents gave the corresponding esters in excellent yields

Arabidopsis cyclin D2 expressed in rice forms a functional cyclin-dependent kinase complex that enhances seedling growth

  • Oh, Se-Jun;Kim, Su-Jung;Kim, Youn Shic;Park, Su-Hyun;Ha, Sun-Hwa;Kim, Ju-Kon
    • Plant Biotechnology Reports
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    • v.2 no.4
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    • pp.227-231
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    • 2008
  • D-class cyclins play important roles in controlling the cell cycle in development and in response to external signals by forming the regulatory subunit of cyclin-dependent kinase (CDK) complexes. To evaluate the effects of D-class cyclins in transgenic rice plants, Arabidopsis cyclin D2 gene (CycD2) was linked to the maize ubiquitin1 promoter (Ubi1) and introduced into rice by the Agrobacterium-mediated transformation method. Genomic deoxyribonucleic acid (DNA), ribonucleic acid (RNA), and Western blot hybridizations of the Ubi1:-CycD2 plants revealed copy number of transgene and its increased expression in leaf and callus cells at messenger RNA (mRNA) and/or protein levels. The H1 kinase assay using the immunoprecipitates of protein extracts from the Ubi1:CycD2 plants and nontransgenic controls demonstrated that the introduced Arabidopsis CycD2 forms a functional CycD2/CDK complex with an unidentified CDK of rice. Shoot and root growth was enhanced in the Ubi1:CycD2 seedlings compared with nontransgenic controls, together, suggesting that Arabidopsis cyclin D2 interacts with a rice cyclin-dependent kinase, consequently enhancing seedling growth.

Notes of 15 unrecorded macrofungi in Korea

  • Minseo Cho;Sun Lul Kwon;Seokyoon Jang;Yeonjae Yoo;Sang Hyun Lee;Dae Young Kwon;Changmu Kim;Young Woon Lim;Jae-Jin Kim
    • Journal of Species Research
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    • v.13 no.1
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    • pp.67-88
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    • 2024
  • Macrofungi are essential decomposers in the forest environment. Although more than 70% of the land is mountainous, there has been a lack of research on mushroom diversity in Korea compared to the global species estimation. For this reason, the need for further research became apparent. The surveys were conducted from 2014 to 2022 nationwide. As a result, 15 unrecorded macrofungal species were discovered: Agaricus thiersii, Baorangia alexandri, Boletellus putuoensis, Entoloma bulakhae, Entoloma pygmaeopapillatum, Entoloma subtenuicystidiatum, Gerronema kuruvense, Hyphoderma nudicephalum, Hyphoderma tenue, Macrolepiota subcitrophylla, Mycena jingyinga, Mycena yuezhuoi, Ophiocordyceps vespulae, Scytinostroma acystidiatum, and Steccherinum straminellum. These species are identified based on morphological, molecular, and phylogenetic analyses using the internal transcribed spacer (ITS) region and the nuclear large subunit rRNA (LSU) region. Here, we provided macro- and micro-morphological figures with phylogenetic trees to support 15 species as unrecorded to Korea.

Growth and Amino Acid Contents of Spirulina platensis with Different Nitrogen Sources

  • Park, Aeran;Kim, Song-Gun;Yoon, Byung-Dae;Oh, Hee-Mock
    • Biotechnology and Bioprocess Engineering:BBE
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    • v.8 no.6
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    • pp.368-372
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    • 2003
  • The growth and amino acid contents of the cyanobacterium, Spirulina platensis strain NIES 46, were investigated using ammonium, nitrate, nitrite, or urea as the sole nitrogen source in a batch culture. Chlorophyll a concentration was highest at 2,096$\mu\textrm{g}$/L in the nitrate group after 10days of cultivation, while the dry weight of S. platensis was highest at 4.5g/L in the ammonium group after 30days of cultivation. The total amino acid content was highest at 174mg/g dry weight of S. platensis in the urea group at the end of the cultivation period, yet the amino acid patterns for S. platensis were similar for all the experimental groups. Therefore, it seemed that the growth and amino acid composition of S. platensis varied depending on the type of nitrogen sources, while the amino acid patterns were not changed. Also, the most efficient harvesting time for S. platensis seemed to be approximately 10 days after cultivation.

Serial Degradation of Perchloroethylene by Delftia sp. N6 after Dechlorination Using Fenton's Reagent

  • Lee, Wan-Seok;Kim, Jang-Eok;Kim, Hee-Sik;Ahn, Chi-Yong;Oh, Hee-Mock
    • Journal of Microbiology and Biotechnology
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    • v.16 no.11
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    • pp.1734-1739
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    • 2006
  • The degradation of perchloroethylene (PCE) was investigated with the serial treatment of biological reaction after dechlorination using Fenton's reagent. The dechlorination of PCE was expressed using $D_m$ (dechlorination value), calculated from ${\Delta}Cl^-mol/{\Delta}PCE$ mol, and was 2.58 with 5 mM of $H_2O_2$ and $Fe^{3+}$. The $150{\mu}M$ of PCE was transformed to $37{\mu}M$ of dichloroacetic acid (DCAA). Biological treatment with Delftia sp. N6 was applied after degradation of PCE by the Fenton reaction. The optical densities indicating cell growth were 0.53/0.10 with/without the Fenton reaction after one day, respectively. The N6 strain degraded 95% of the DCAA produced from PCE by the Fenton reaction within one day. Consequently, it seemed that the serial treatment of a Fenton reaction and biological reaction was effective in the removal of not only PCE, but also DCAA, one of the major metabolites of PCE.