• 제목/요약/키워드: glutamicum

검색결과 153건 처리시간 0.037초

초산을 이용한 글루타민산의 발효생산에 관한 연구 제 1보 글루타민산 생산균주의 분리 및 동정 (Studies on the Bacterial Production of L-Glutamate from Acetate Part I. Screening and Identification of L-Glutamate Producing Bacteria.)

  • 하덕모;노완섭
    • 한국미생물·생명공학회지
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    • 제2권2호
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    • pp.103-109
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    • 1974
  • 전국 각지대의 279개소의 토양시료로 부터 초산자화성세균 383균주를 분리하였으며 이들 초산자화성세균중 L-GA생성 능이 우수한 5균주를 선정하고 균학적성질을 조사하여 Brebacterium flavum nov. sp. D1005B, Corynebacterium glutamicum nov. sp. D1025A, Brevibacterium. flavum nov. sp. D2209B, Corynebacterium acetoacidophilum nov. sp. D2212B 및 Corynebacterium acetoacidophilum nov. sp. D2349A로 동정 명명하였다

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Generation of Minicells from an Endotoxin-Free Gram-Positive Strain Corynebacterium glutamicum

  • Lee, Jin-Young;Choy, Hyon E.;Lee, Jin-Ho;Kim, Geun-Joong
    • Journal of Microbiology and Biotechnology
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    • 제25권4호
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    • pp.554-558
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    • 2015
  • Drug delivery systems (DDSs) incorporating bacterial minicells have been evaluated as a very powerful tool in view of biocompatibility. However, limited studies have been carried out on these systems, mainly using minicells from Salmonella sp. and Escherichia coli. Thus, we generated a new minicell-producing strain from an endotoxin-free Corynebacterium glutamicum by the inactivation of genes related to cell division. The two knockout strains, ${\Delta}parA$ and ${\Delta}ncgl1366$, showed distinct abilities to produce minicells. The resulting minicells were purified via sequential antibiotic treatments and centrifugations, which resulted in reproducible yields.

Corynebacteria-E. coli shuttle vector pKU6의 분리 및 확인 (Isolation and characterization of corynebacteria-E. coli shuttle vector pKU6 from coryneform bacteria)

  • 허태린;이진우;이세영
    • 미생물학회지
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    • 제22권4호
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    • pp.249-255
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    • 1984
  • To develop the host-vector system for industrial Coryneform bacteria that seemed to be the most suitable microorganisms for molecular breeding of genes involved in the production of amion acids, nucleotides, and other products of industrial interest, broad host range E. coli plasmid R 1162 DNA was transformed into Brevibacterium ammoniagenes and the plasmids pKU6 isolated from a transformant was physically characterized. All other plasmids from the transformed cells except pKU6 exsisted as multimeric forms in Brevibacterium ammoniagenes. The plasmid DNA was retransformed into Corynebacterium glutamicum with a high frequency ($1.32{\times}10^{-1}$ per cell) and maintained stably both in Brevibacterium ammoniagenes and Corynebacterium glutamicum after 100 generations of cultures with 25-30 copy number per cell. The size of both plasmid pKU6 and plasmid R1162 were the same and restriction maps by EcoR I, Ava I, Pst I, Pvu II and Hinc II were also similar.

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