scholarly journals Enhanced Spore Production of <i>Bacillus subtilis</i> Grown in a Chemically Defined Medium

2014 ◽  
Vol 04 (08) ◽  
pp. 444-454 ◽  
Author(s):  
S. M. S. Monteiro ◽  
J. J. Clemente ◽  
M. J. T. Carrondo ◽  
A. E. Cunha
2004 ◽  
Vol 70 (3) ◽  
pp. 1869-1873 ◽  
Author(s):  
Hengameh van der Kaaij ◽  
Frank Desiere ◽  
Beat Mollet ◽  
Jacques-Edouard Germond

ABSTRACT Using a chemically defined medium without l-alanine, Lactobacillus johnsonii was demonstrated to be strictly auxotrophic for that amino acid. A comparative genetic analysis showed that all known genes involved in l-alanine biosynthesis are absent from the genome of L. johnsonii. This auxotrophy was complemented by heterologous expression of the Bacillus subtilis l-alanine dehydrogenase.


1965 ◽  
Vol 97 (2) ◽  
pp. 573-578 ◽  
Author(s):  
HJ Rogers ◽  
GGF Newton ◽  
EP Abraham

1. Bacilysin, a hydrophilic substance formed by certain aerobic spore-forming bacteria that causes lysis in cultures of growing staphylococci, has been produced in aerated cultures of a strain of Bacillus subtilis (A14). A chemically defined medium was used, which contained glucose, Czapek-Dox salts and ferric iron. Production of bacilysin occurred, after a lag, while the culture was still undergoing rapid growth. 2. Bacilysin was adsorbed from the culture medium on Zeo-Karb 225 (SR5) (H(+) form) and eluted with aqueous pyridine. The crude material was purified by chromatography in pyridine-acetate buffers on columns of Dowex 50 (X2) and Dowex 50 (X8) respectively and by chromatography in aq. 70% (v/v) propan-2-ol on Sephadex G-25. 3. Purified bacilysin behaved as a single ninhydrin-positive substance when subjected to chromatography on paper in butan-1-ol-acetic acid-water and to electrophoresis on paper at pH4.5 or pH1.8. At pH4.5 the substance behaved as though it had no net change and at pH1.8 it migrated towards the cathode.


1968 ◽  
Vol 25 (3) ◽  
pp. 547-553 ◽  
Author(s):  
G. A. Strasdine ◽  
Joanne Melville

A chemically defined medium is described for the growth and spore production of Clostridium botulinum type E, strain Minnesota. With the exception of valine, omitting any amino acid or vitamin did not prevent growth, although marked changes in morphology or reduced growth were usually evident. Choline was shown to be an essential factor in promoting cell division and was capable of exerting this action after maximum growth was attained. Spore development in the medium was markedly influenced by the source of available carbon and ranged from complete sporulation of cultures grown on maltose and glucose to complete inhibition with galactose.


2021 ◽  
Author(s):  
Sebastián Cerminati ◽  
Mélanie Leroux ◽  
Pablo Anselmi ◽  
Salvador Peirú ◽  
Juan C. Alonso ◽  
...  

AbstractHyaluronic acid (HA) is a high value glycosaminoglycan mostly used in health and cosmetic applications. Commercial HA is produced from animal tissues or in toxigenic bacteria of the genus Streptococcus grown in complex media, which are expensive and raise environmental concerns due to the disposal of large amounts of broth with high organic loads. Other microorganisms were proposed as hosts for the heterologous production of HA, but the methods are still costly. The extraordinary capacity of this biopolymer to bind and retain water attracts interest for large scale applications where biodegradable materials are needed, but its high cost and safety concerns are barriers for its adoption.Bacillus subtilis 3NA strain is prototrophic, amenable for genetic manipulation, GRAS, and can rapidly reach high cell densities in salt-based media. These phenotypic traits were exploited to create a platform for biomolecule production using HA as a proof of concept. First, the 3NA strain was engineered to produce HA; second, a chemically defined medium was formulated using commodity-priced inorganic salts combined at the stoichiometric ratios needed to build the necessary quantities of biomass and HA; and third, a scalable fermentation process, where HA can be produced at the maximum volumetric productivity (VP), was designed.A comparative economic analysis against other methods indicates that the new process may increase the operating profit of a manufacturing plant by more than 100 %. The host, the culture medium, and the rationale employed to develop the fermentation process described here, introduce an IP free platform that could be adaptable for production of other biomolecules.Key PointsA platform for the production of biomolecules was designed based on B. subtilis 3NA, a chemically defined medium and a fermentation process.As proof of concept, high quality hyaluronic acid was produced with an environmentally friendly process.A techno-economic analysis indicates that the process is more that 100% profitable than current methods.


2012 ◽  
Vol 78 (9) ◽  
pp. 2120-2128 ◽  
Author(s):  
M.M. Vick ◽  
H.L. Bateman ◽  
C.A. Lambo ◽  
W.F. Swanson

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