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Merck
CN

MBD0055

Sigma-Aldrich

MediaBoost

new

non-animal sterile microbial growth supplement

别名:

growth supplement for germination, microbial culture additive, microbial culture enhancer, microbial media supplement, minimal growth media supplement

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About This Item

UNSPSC代码:
41106212
NACRES:
NB.21

质量水平

无菌性

sterile

形式

liquid

技术

microbiological culture: suitable

运输

wet ice

储存温度

2-8°C

适用性

Bacillus spp.
Escherichia spp.
Lactobacillus spp.
Lactococcus spp.
Pseudomonas spp.
Saccharomyces spp.
bacteria
yeasts

一般描述

Studying microbial species via cutting edge genomic techniques such as next generation sequencing (NGS) has become increasingly prevalent in recent years; however, genomic methods alone cannot fully replace experimental testing of microbial species. Therefore, the ability to culture microbes in a laboratory setting remains essential for comprehensive study of these communities. Some microbial species can be challenging to culture in standard culture media. Often species of interest or a specific process require specialized media compositions, to provide an optimal environment for maximal proliferation and yield. A few examples includes

  • Chemically defined minimal growth media are often used to grow bacteria for proteomics, as a base for stable isotope enrichment in NMR protein structure-function studies, but growth can be limited without the addition of an effective supplement.

  • Use of chemically defined minimal growth media in the production of secreted microbial proteins to ensure reproducibility and a higher concentration of the microbial-produced protein of interest.

应用

MediaBoost provides microbial researchers a ready-to-use media supplement to amplify growth in selected gram-positive bacteria, gram-negative bacteria, and yeast species. Application data is available for some of the strains and media combinations that have been tested with MediaBoost, including:
  • Bacillus subtilis spores in LB medium
  • Lactobacillus rhamnosus in LB medium
  • Pseudomonas aeruginosa in M9 medium
  • Saccharomyces cerevisiae in YPD, BM2, and IMDM media

Please note strains and media combinations and should be tested on a case-by-case basis by the researcher for experiment optimization.

特点和优势

  • Boosts Growth of Certain Microorganisms
  • Reduces Germination Time
  • Ready-Made, Sterile Solution
  • Protein-Free

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

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Jean-Christophe Lagier et al.
Clinical microbiology reviews, 28(1), 208-236 (2015-01-09)
A pure bacterial culture remains essential for the study of its virulence, its antibiotic susceptibility, and its genome sequence in order to facilitate the understanding and treatment of caused diseases. The first culture conditions empirically varied incubation time, nutrients, atmosphere
William H Lewis et al.
Nature reviews. Microbiology, 19(4), 225-240 (2020-10-24)
Despite the surge of microbial genome data, experimental testing is important to confirm inferences about the cell biology, ecological roles and evolution of microorganisms. As the majority of archaeal and bacterial diversity remains uncultured and poorly characterized, culturing is a
M Bonnet et al.
New microbes and new infections, 34, 100622-100622 (2020-01-21)
Microbiology has been largely developed thanks to the discovery and optimization of culture media. The first liquid artificial culture medium was created by Louis Pasteur in 1860. Previously, bacterial growth on daily materials such as some foods had been observed.
Maryam Tidjani Alou et al.
Clinical microbiology reviews, 34(1) (2020-10-30)
The last 5 years have seen a turning point in the study of the gut microbiota with a rebirth of culture-dependent approaches to study the gut microbiota. High-throughput methods have been developed to study bacterial diversity with culture conditions aimed
Anna Gąciarz et al.
Microbial cell factories, 16(1), 108-108 (2017-06-18)
The production of recombinant proteins containing disulfide bonds in Escherichia coli is challenging. In most cases the protein of interest needs to be either targeted to the oxidizing periplasm or expressed in the cytoplasm in the form of inclusion bodies

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