Literature DB >> 14188708

USE OF ARTHROBACTER TERREGENS FOR BIOASSAY OF MYCOBACTIN.

C V REICH, J H HANKS.   

Abstract

Reich, Claude V. (Johns Hopkins-Leonard Wood Memorial Leprosy Research Laboratory, Johns Hopkins University, Baltimore, Md.), and John H. Hanks. Use of Arthrobacter terregens for bioassay of mycobactin. J. Bacteriol. 87:1317-1320. 1964.-Arthrobacter terregens was used to assay mycobactin, a growth factor for Mycobacterium paratuberculosis. Within 7 days, A. terregens gave a linear photometric growth response to mycobactin in the range of 0.05 to 0.2 mug/ml. Preparations found to be active (or inactive) by this assay produced corresponding effects on the growth of M. paratuberculosis after 6 weeks to 4 months. Mycobactin was produced routinely from pellicles of M. phlei on a peptone-glycerol-beef heart infusion medium, and was extracted from both cells and medium by organic solvents. The mycobactin content per cell rose rapidly after the third day and attained a maximum at 4 to 6 days. The decline to less than one-half this value by the tenth day was associated with excretion into the medium. Production on synthetic media occurred after increasing the usual levels of asparagine. The demonstrated effects of crude mycobactin on the donor strain were (i) to catalyze the onset of growth and (ii) to reverse the effect of conditions which cause the formation of abnormal cells.

Entities:  

Keywords:  ARTHROBACTER; BIOLOGICAL ASSAY; GROWTH SUBSTANCES; MYCOBACTERIUM

Mesh:

Substances:

Year:  1964        PMID: 14188708      PMCID: PMC277205          DOI: 10.1128/jb.87.6.1317-1320.1964

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  6 in total

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2.  Some aspects of microbial iron metabolism.

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Journal:  Bacteriol Rev       Date:  1957-06

3.  Soil bacteria and growth-promoting substances.

Authors:  A G LOCHHEAD
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4.  Studies on the isolation and nature of the terregens factor.

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5.  Mycobactin, a growth factor for Mycobacterium johnei. I. Isolation from Mycobacterium phlei.

Authors:  J FRANCIS; H M MACTURK; J MADINAVEITIA; G A SNOW
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6.  Modifications of Dubos's media for the cultivation of Mycobacterium johnei.

Authors:  H W SMITH
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  6 in total
  14 in total

1.  LABORATORY INFECTION WITH A LACTOSE-FERMENTING STRAIN OF SALMONELLA TYPHI.

Authors:  L J KUNZ; W H EWING
Journal:  J Bacteriol       Date:  1965-06       Impact factor: 3.490

2.  SYNTHETIC METAL CHELATORS WHICH REPLACE THE NATURAL GROWTH-FACTOR REQUIREMENTS OF ARTHROBACTER TERREGENS.

Authors:  N E MORRISON; A D ANTOINE; E E DEWBREY
Journal:  J Bacteriol       Date:  1965-06       Impact factor: 3.490

Review 3.  Mycobactins: iron-chelating growth factors from mycobacteria.

Authors:  G A Snow
Journal:  Bacteriol Rev       Date:  1970-06

Review 4.  Host-dependent microbes.

Authors:  J H Hanks
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5.  Absence of siderophore activity in Legionella species grown in iron-deficient media.

Authors:  M W Reeves; L Pine; J B Neilands; A Balows
Journal:  J Bacteriol       Date:  1983-04       Impact factor: 3.490

6.  Growth factor activity of mycobactin for Arthrobacter species.

Authors:  N E Morrison; E E Dewbrey
Journal:  J Bacteriol       Date:  1966-12       Impact factor: 3.490

7.  Assay of the mycobactins by measurement of the growth of Mycobacterium johnei.

Authors:  D W Wheather; G A Snow
Journal:  Biochem J       Date:  1966-07       Impact factor: 3.857

8.  Iron-chelating hydroxamic acid (schizokinen) active in initiation of cell division in Bacillus megaterium.

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9.  Iron acquisition by Neisseria meningitidis in vitro.

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10.  Response of Neisseria gonorrhoeae to iron limitation: alterations in expression of membrane proteins without apparent siderophore production.

Authors:  S E West; P F Sparling
Journal:  Infect Immun       Date:  1985-02       Impact factor: 3.441

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