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產(chǎn)品目錄
  • 細(xì)胞培養(yǎng)進(jìn)口血清
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    支原體DNA提取
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    特異性標(biāo)準(zhǔn)品(方法驗(yàn)證用)
    PCR定量標(biāo)準(zhǔn)品(可用于方法驗(yàn)證)
  • 支原體祛除試劑
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    環(huán)境支原體祛除
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    DNA污染監(jiān)測(cè)祛除
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    熱啟動(dòng)聚合酶MB Taq DNA
  • 微生物PCR檢測(cè)
    食品檢測(cè)類(lèi)產(chǎn)品
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利用微生物培養(yǎng)基的景觀來(lái)預(yù)測(cè)新的有機(jī)體媒體配對(duì)

2016-09-27 14:39

The most frequently altered compounds in this way are the biologically common ions/salts, followed by trace metals and vitamins. This lends further evidence that these trace components play key roles in differentiating growth between close species, and thus should be considered in future media design.

Beyond these analyses, we examine broad trends in compound usage across phyla at different taxonomic levels. Heat maps of enrichment of different taxonomic groups for media components can be found in Supplementary Figs 4–8 and Supplementary Note 3.

Media usage follows phylogenetic and ecological trends

An implicit assumption that investigators make when trying to cultivate new microorganisms is that the best medium to start with is one from a phylogenetic or ecological neighbour. Despite its apparent logic, this assumption has not, to our knowledge, been rigorously tested and validated. To do this, we mapped organisms in DSMZ to operational taxonomic units in Greengenes ecological data as clustered into environments (see Methods for details; clustering in ref. 20), and also to taxonomic classifications from the Interactive Tree of Life project (Itol21). We find that, indeed, the likelihood that two organisms share at least one lab medium strongly correlates with both their ecological and phylogenetic similarity (see Fig. 3; ρ=0.76, P=2.3e?13, and ρ=0.92, P=1.3e?3, respectively, for ecological and phylogenetic similarities, as determined by cohabitation Jaccard index (ecological) or inverse subtree count in the iTOL taxonomic tree (phylogenetic); see Methods for details). This indicates that phylogenetic and ecological closeness are good heuristics for determining the likelihood that two organisms have successfully been grown in the same lab medium. Indeed, we show later that this is not just descriptive of what has been done in the past, but that it holds a signal that can be used predictively for deriving new successful organism–media pairings. Importantly, the fractions of organism pairs sharing lab media listed in Fig. 3 are likely underestimates, as the organism-by-media matrix in KOMODO is highly underpopulated (see previous section). This observation is indeed upheld when we perform new growth experiments, as most of our predictions (which were not listed previously in KOMODO) yield growth.

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