Babbar Shashi B, Jain Ruchi
Department of Botany, University of Delhi, Delhi, India.
Curr Microbiol. 2006 Apr;52(4):287-92. doi: 10.1007/s00284-005-0225-5. Epub 2006 Mar 18.
Xanthan gum, microbial desiccation-resistant polysaccharide prepared commercially by aerobic submerged fermentation from Xanthomonas campestris, has been successfully used alone and in combination with agar for microbial culture media. As illustrative examples, eight bacteria and eight fungi were grown on media solidified with either agar (A, 1.5%), xanthan gum (X, 1%), or combinations of both (0.9% X + 0.1% A, 0.8% X + 0.2% A, 0.7% X + 0.3% A, 0.6% X + 0.4% A). All fungi and bacteria exhibited normal growth and differentiation in all these treatments. Rather, growth of most of the fungi was better on xanthan (alone) and xanthan + agar media than agar medium. As the media gelled with xanthan gum alone flow, it was not possible to incubate Petri plates in inverted position. Moreover, because of the softness, streaking of bacteria was difficult on such media. However, these problems could be overcome by partially replacing xanthan gum with 0.3% agar. Bacterial enumeration studies carried out for Serratia sp. and Pseudomonas sp. by serial dilution and pour-plate method on agar (1.5%), 0.7%/0.6% X + 0.3%/0.4% A yielded similar counts. Selective media, succinate medium for Pseudomonas sp., and MacConkey broth medium for Escherichia coli gelled with 0.7%/0.6% X + 0.3%/0.4% A did not support growth of other bacteria when inoculated along with the above-mentioned bacteria. Likewise, differential medium, CRMA (Congo red mannitol agar) gelled with xanthan-agar combination could differentiate between Agrobacterium tumefaciens and Rhizobium sp.
黄原胶是一种通过甘蓝黑腐病黄单胞菌有氧深层发酵商业制备的微生物抗干燥多糖,已成功单独使用或与琼脂结合用于微生物培养基。作为示例,将八种细菌和八种真菌接种在分别用琼脂(A,1.5%)、黄原胶(X,1%)或两者组合(0.9% X + 0.1% A、0.8% X + 0.2% A、0.7% X + 0.3% A、0.6% X + 0.4% A)固化的培养基上培养。所有真菌和细菌在所有这些处理中均表现出正常生长和分化。相反,大多数真菌在黄原胶(单独)和黄原胶 + 琼脂培养基上的生长比在琼脂培养基上更好。由于仅用黄原胶凝胶化的培养基会流动,因此无法将培养皿倒置培养。此外,由于其柔软性,在这种培养基上进行细菌划线接种很困难。然而,用0.3%的琼脂部分替代黄原胶可以克服这些问题。通过在琼脂(1.5%)、0.7%/0.6% X + 0.3%/0.4% A上采用系列稀释和平板倾注法对粘质沙雷氏菌和铜绿假单胞菌进行细菌计数研究,得到了相似的计数结果。用0.7%/0.6% X + 0.3%/0.4% A凝胶化的选择性培养基(用于铜绿假单胞菌的琥珀酸盐培养基)和用于大肠杆菌的麦康凯肉汤培养基,在与上述细菌一起接种时,不支持其他细菌生长。同样,用黄原胶 - 琼脂组合凝胶化的鉴别培养基CRMA(刚果红甘露醇琼脂)可以区分根癌土壤杆菌和根瘤菌属。