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      KCI등재 SCOPUS

      분산변이주 Archangium gephyra KYC5002의 자실체 발달과 포자 형성에 대한 정량적 분석 = Quantitative analysis of the fruiting body development and sporulation of the dispersion mutant Archangium gephyra KYC5002

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      https://www.riss.kr/link?id=A108414685

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Fruiting body development and glycerol spore formation of the myxobacterium Archangium gephyra have been quantitatively analyzed using the KYC5002 strain, which grows in a dispersed manner in liquid media. KYC5002 formed many fruiting bodies that are smaller in size than those of the wild-type strain on various agar media and developed the most intact fruiting bodies on MMC agar plates composed of 10 mM 3-morpholinopropane- 1-sulfonic acid, 8 mM MgSO4, 0.015% casitone, and 3% agar.
      Fruiting bodies developed when the cell suspension concentration was 5 × 108–5 × 109 cells/ml, but no fruiting bodies were formed at cell suspension concentrations higher or lower than that. The long and thin vegetative cells transformed into thick and short fruiting body spores in the fruiting bodies. Transformation into glycerol spores was possible at all time points in liquid culture, but it was achieved with high efficiency during the period of vigorous cell growth, yet with low efficiency during the stationary phase. The produced glycerol spores were morphologically similar to the fruiting body spores, and showed resistance to ultrasound and heat; however, its heat resistance was lower than that of the spores of the fruiting body.
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      Fruiting body development and glycerol spore formation of the myxobacterium Archangium gephyra have been quantitatively analyzed using the KYC5002 strain, which grows in a dispersed manner in liquid media. KYC5002 formed many fruiting bodies that are ...

      Fruiting body development and glycerol spore formation of the myxobacterium Archangium gephyra have been quantitatively analyzed using the KYC5002 strain, which grows in a dispersed manner in liquid media. KYC5002 formed many fruiting bodies that are smaller in size than those of the wild-type strain on various agar media and developed the most intact fruiting bodies on MMC agar plates composed of 10 mM 3-morpholinopropane- 1-sulfonic acid, 8 mM MgSO4, 0.015% casitone, and 3% agar.
      Fruiting bodies developed when the cell suspension concentration was 5 × 108–5 × 109 cells/ml, but no fruiting bodies were formed at cell suspension concentrations higher or lower than that. The long and thin vegetative cells transformed into thick and short fruiting body spores in the fruiting bodies. Transformation into glycerol spores was possible at all time points in liquid culture, but it was achieved with high efficiency during the period of vigorous cell growth, yet with low efficiency during the stationary phase. The produced glycerol spores were morphologically similar to the fruiting body spores, and showed resistance to ultrasound and heat; however, its heat resistance was lower than that of the spores of the fruiting body.

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      참고문헌 (Reference)

      1 Galván A, "Ultrastructure of natural and induced myxospores of Archangium gephyra" 38 : 130-134, 1992

      2 Sasse F, "Tubulysins, new cytostatic peptides from myxobacteria acting on microtubuli. Production, isolation, physico-chemical and biological properties" 53 : 879-885, 2000

      3 Shimkets LJ, "The Prokaryotes" Springer 31-115, 2006

      4 Reichenbach H, "Structural changes in Stigmatella aurantiaca during myxospore induction" 97 : 905-911, 1969

      5 Flärdh K, "Streptomyces morphogenetics : dissecting differentiation in a filamentous bacterium" 7 : 36-49, 2009

      6 O’Connor KA, "Starvation-independent sporulation in Myxococcus xanthus involves the pathway for β-lactamase induction and provides a mechanism for competitive cell survival" 24 : 839-850, 1997

      7 Shimkets LJ, "Social and developmental biology of the myxobacteria" 54 : 473-501, 1990

      8 현혜숙 ; Choi Juo ; 강다은 ; 김영필 ; 이필구 ; Gregory J. Y. Chung ; 조경연, "Screening of Myxobacteria Carrying Tubulysin Biosynthetic Genes" 한국미생물·생명공학회 49 (49): 32-38, 2021

      9 Sudo SZ, "Resistance of vegetative cells and microcysts of Myxococcus xanthus" 98 : 883-887, 1969

      10 Higgins D, "Recent progress in Bacillus subtilis sporulation" 36 : 131-148, 2012

      1 Galván A, "Ultrastructure of natural and induced myxospores of Archangium gephyra" 38 : 130-134, 1992

      2 Sasse F, "Tubulysins, new cytostatic peptides from myxobacteria acting on microtubuli. Production, isolation, physico-chemical and biological properties" 53 : 879-885, 2000

      3 Shimkets LJ, "The Prokaryotes" Springer 31-115, 2006

      4 Reichenbach H, "Structural changes in Stigmatella aurantiaca during myxospore induction" 97 : 905-911, 1969

      5 Flärdh K, "Streptomyces morphogenetics : dissecting differentiation in a filamentous bacterium" 7 : 36-49, 2009

      6 O’Connor KA, "Starvation-independent sporulation in Myxococcus xanthus involves the pathway for β-lactamase induction and provides a mechanism for competitive cell survival" 24 : 839-850, 1997

      7 Shimkets LJ, "Social and developmental biology of the myxobacteria" 54 : 473-501, 1990

      8 현혜숙 ; Choi Juo ; 강다은 ; 김영필 ; 이필구 ; Gregory J. Y. Chung ; 조경연, "Screening of Myxobacteria Carrying Tubulysin Biosynthetic Genes" 한국미생물·생명공학회 49 (49): 32-38, 2021

      9 Sudo SZ, "Resistance of vegetative cells and microcysts of Myxococcus xanthus" 98 : 883-887, 1969

      10 Higgins D, "Recent progress in Bacillus subtilis sporulation" 36 : 131-148, 2012

      11 Komano T, "Patterns of protein production in Myxococcus xanthus during spore formation induced by glycerol, dimethyl sulfoxide, and phenethyl alcohol" 144 : 1076-1082, 1980

      12 Dworkin M, "Nutritional requirements for vegetative growth of Myxococcus xanthus" 84 : 250-257, 1962

      13 현혜숙 ; 최주오 ; 안동주 ; 조경연, "Myxococcus stipitatus의 자실체 형성을 위한 배지 조성" 한국미생물학회 55 (55): 117-122, 2019

      14 Shi W, "Molecular Micro-biology Techniques" Academic Press 258-269, 1994

      15 Sasse F, "Melithiazols, new β-methoxyacrylate inhibitors of the respiratory chain isolated from myxobacteria" 52 : 721-729, 1999

      16 김재헌 ; 한광용 ; 정호진 ; 이정남, "Iron Containing Superoxide Dismutase of Streptomyces subrutilus P5 Increases Bacterial Heavy Metal Resistance by Sequestration" 한국미생물학회 50 (50): 179-184, 2014

      17 Dworkin M, "Induction of cellular morphogenesis in Myxococcus xanthus I" 91 : 1516-1519, 1966

      18 Sasse F, "Gephyronic acid, a n ovel i nhibitor o f euka ryotic p rotein s ynthesis f rom Archangium gephyra(myxobacteria)" 48 : 21-25, 1995

      19 최주오 ; Park Taejoon ; Kang Daun ; Lee Jeongju ; Kim Yungpil ; Lee Pilgoo ; Chung Gregory J. Y. ; 조경연, "Discovery of Argyrin-Producing Archangium gephyra MEHO_001 and Identification of Its Argyrin Biosynthetic Genes" 한국미생물·생명공학회 49 (49): 493-500, 2021

      20 신혜진 ; 윤진권 ; 안동주 ; 조경연, "Corallococcus와 Myxococcus 속 점액세균 균주들에 의한 항균 물질의 생산" 한국미생물·생명공학회 41 (41): 44-51, 2013

      21 Inouye M, "Biosynthesis and self-assembly of protein S, a development-specific protein of Myxococcus xanthus" 76 : 209-213, 1979

      22 Dawid W, "Biology and global distribution of myxobacteria in soil" 24 : 403-427, 2000

      23 Reichenbach H, "Bergey's Manual of Systematic Bacteriology" 1059-1144, 2005

      24 Kunze B, "Aurafuron A and B, new bioactive polyketides from Stigmatella aurantiaca and Archangium gephyra(Myxobacteria)" 58 : 244-251, 2005

      25 Sasse F, "Argyrins, immunosuppressive cyclic peptides from myxobacteria" 55 : 543-551, 2002

      26 Sasse F, "Archazolids, new cytotoxic macrolactones from Archangium gephyra(Myxobacteria)" 56 : 520-525, 2003

      27 O’Connor KA, "Analysis of Myxococcus xanthus cell types by two-dimensional polyacrylamide gel electrophoresis" 173 : 3334-3341, 1992

      28 Dworkin M, "A system for studying microbial morphogenesis : rapid formation of microcysts in Myxococcus xanthus" 146 : 243-244, 1964

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