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US4452890A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of producing L-threonine by fermentation

Assignee: Ajinomoto Co Inc
•
Filing: 1982-05-10
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Granted: 1984-06-05
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Expires: 2002-05-10
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Abstract

Abstract An L-threonine microorganism is produced by inserting a restriction endonuclease fragment of chromosomal DNA controlling α-amino-β-hydroxy valeric acid resistance from a Brevibacterium or Corynebacterium into a plasmid and transforming a Brevibacterium or Corynebacterium which is sensitive to α-amino-β-hydroxy valeric acid.

Inventors

  • 👤 Takayasu Tsuchida
  • 👤 Kiyoshi Miwa
  • 👤 Shigeru Nakamori

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 18:19
CPC Classifications
C; C12; C12N; C12N15/00; C12N15/09; C12N15/63; C12N15/74; C12N15/77; C12N15/11; C12N15/52; C12P; C12P13/00; C12P13/04; C12P13/08

Claims Analysis

Total Claims: 12
Claim 1
Independent Claim 109 words
A method for producing L-threonine by fermentation which comprises aerobically culturing in an aqueous culture medium an L-threonine producing microorganism obtained by isolating a strain transformed to become resistant to α-amino-β-hydroxy-valeric acid after incorporation into a recipient strain of the genus Brevibacterium or Corynebacterium which is sensitive to α-amino-β-hydroxy valeric acid, of a plasmid DNA obtained from a microorganism of the genus Brevibacterium or Corynebacterium and having been inserted therein a restriction endonuclease fragment of chromosomal DNA controlling α-amino-β-hydroxy valeric acid resistance derived from a DNA-donor strain of the genus Brevibacterium or Corynebacterium which is resistant to α-amino-β-hydroxy valeric acid, and recovering L-threonine accumulated in the resulted culture liquid.
Claim 2
Independent Claim 109 words
A method for producing L-threonine by fermentation which comprises aerobically culturing in an aqueous culture medium an L-threonine producing microorganism obtained by isolating a strain transformed to become resistant to α-amino-β-hydroxy-valeric acid after incorporation into a recipient strain of the genus Brevibacterium or Corynebacterium which is sensitive to α-amino-β-hydroxy valeric acid, of a plasmid DNA obtained from a microorganism of the genus Brevibacterium or Corynebacterium and having been inserted therein a restriction endonuclease fragment of chromosomal DNA controlling α-amino-β-hydroxy valeric acid resistance derived from a DNA-donor strain of the genus Brevibacterium or Corynebacterium which is resistant to α-amino-β-hydroxy valeric acid, and recovering L-threonine accumulated in the resulted culture liquid.
Claim 3
Dependent Claim 16 words
The method of claim 1, wherein said recipient strain belongs to Brevibacterium lactofermentum or Corynebacterium glutamicum.
Claim 4
Dependent Claim 16 words
The method of claim 1, wherein said DNA-donor strain belongs to Brevibacterium lactofermentum or Corynebacterium glutamicum.
Claim 5
Dependent Claim 22 words
The method of claim 1, wherein said DNA-donor strain is resistant to an amount of α-amino-β-hydroxyvaleric acid or more than 100 μg/ml.
Claim 6
Dependent Claim 18 words
The method of claim 1, wherein said L-threonine producing microoganism is Corynebacterium glutamicum FERM-P5973=FERM-BP119 or Brevibacterium lactofermentum FERM-P5974=FERM-BP119.
Claim 7
Independent Claim 99 words
A method for constructing an L-threonine producing strain which comprises: (a) separating a plasmid DNA from a microorganism of the genus Brevibacterium and Corynebacterium, (b) inserting into the plasmid DNA a restriction endonuclease fragment of chromosomal DNA controlling α-amino-β-hydroxy valeric acid resistance derived from a DNA-donor strain of the genus Brevibacterium or Corynebacterium resistant to α-amino-β-hydroxy valeric acid to obtain a recombinant plasmid DNA (c) incorporating the recombinant plasmid DNA into a recipient strain of the genus Brevibacterium or Corynebacterium which is sensitive to α-amino-β-hydroxy valeric acid, and (d) isolating a strain transformed to become resistant to α-amino-β-hydroxy-valeric acid.
Claim 8
Independent Claim 99 words
A method for constructing an L-threonine producing strain which comprises: (a) separating a plasmid DNA from a microorganism of the genus Brevibacterium and Corynebacterium, (b) inserting into the plasmid DNA a restriction endonuclease fragment of chromosomal DNA controlling α-amino-β-hydroxy valeric acid resistance derived from a DNA-donor strain of the genus Brevibacterium or Corynebacterium resistant to α-amino-β-hydroxy valeric acid to obtain a recombinant plasmid DNA (c) incorporating the recombinant plasmid DNA into a recipient strain of the genus Brevibacterium or Corynebacterium which is sensitive to α-amino-β-hydroxy valeric acid, and (d) isolating a strain transformed to become resistant to α-amino-β-hydroxy-valeric acid.
Claim 9
Dependent Claim 16 words
The method of claim 6, wherein said recipient strain belongs to Brevibacterium lactofermentum or Corynebacterium glutamicum
Claim 10
Dependent Claim 16 words
The method of claim 6, wherein said DNA-donor strain belongs to Brevibacterium lactofermentum or Corynebacterium glutamicum.
Claim 11
Dependent Claim 21 words
The method of claim 6, wherein said DNA-donor strain is resistant to an amount of L-threonine of more than 1000 μg/ml.
Claim 12
Dependent Claim 18 words
The method of claim 6, wherein said L-threonine producing microorganism is Corynebacterium glutamicum FERM-P5973=FERM-BP118 or Brevibacterium lactofermentum FERM-P5974=FERM-BP119.

References Cited (Backward Citations)

US3732144A Cited
US4347318A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-06-05 1987-12-05 1988-06-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-06-05 1991-12-05 1992-06-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-06-05 1995-12-05 1996-06-05 $7700.00 Window Closed / Lapsed

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