Université Européenne de Bretagne, France.
Int J Food Microbiol. 2010 Mar 31;138(1-2):100-7. doi: 10.1016/j.ijfoodmicro.2009.12.013. Epub 2009 Dec 16.
Real-time PCR has been applied to quantify mycelium of Penicillium camemberti and Penicillium roqueforti during ripening of model cheese curd and surface mould-ripened cheeses. Total fungal DNA was first validated as an indicator of mycelial biomass in pure liquid culture and then in model curds at different stages of ripening. To imitate cheese matrix effects, DNA was extracted from curd mixed with known amounts of fresh mycelium of P. camemberti or P. roqueforti and was used as biomass standards for further quantitative real-time PCR. Mycelial mass per cheese (mg/g) was then directly obtained from fluorescence data. In model cheese curd, mycelial mass of P. camemberti increased from 2.8 at d4 to 596 mg/g at d11 whereas P. roqueforti increased from 0.3 to 6.3 mg/g during the same period. P. camemberti showed a fast development in Coulommiers from d2 to d9 (66 to 119 mg/g) and a 100-fold increase in Carré (0.85 to 85 mg/g). While mycelial biomass reached a maximum at d9 in Coulommiers, it still developed in Carré until d45. For the first time, cheese manufacturers have a powerful technique to monitor mycelial growth dynamics of their fungal cultures, which represents an important step for controlling cheese making.
实时 PCR 已被应用于定量测定干酪凝乳和表面模制奶酪成熟过程中 Penicillium camemberti 和 Penicillium roqueforti 的菌丝体。总真菌 DNA 首先在纯液体培养中验证为菌丝体生物量的指标,然后在不同成熟阶段的模型凝乳中验证。为了模拟奶酪基质的影响,从凝乳中提取 DNA,凝乳中混合有已知量的新鲜 P. camemberti 或 P. roqueforti 菌丝体,并用作进一步定量实时 PCR 的生物量标准。然后,从荧光数据直接获得每块奶酪的菌丝体质量(mg/g)。在模型干酪凝乳中,P. camemberti 的菌丝体质量从第 4 天的 2.8mg/g 增加到第 11 天的 596mg/g,而 P. roqueforti 的菌丝体质量从第 4 天的 0.3mg/g 增加到第 11 天的 6.3mg/g。P. camemberti 在 Coulommiers 中从第 2 天到第 9 天(66 至 119mg/g)快速发展,并在 Carré 中增加了 100 倍(0.85 至 85mg/g)。虽然在 Coulommiers 中菌丝体生物量在第 9 天达到最大值,但在 Carré 中仍在继续发展,直到第 45 天。对于奶酪制造商来说,这是首次拥有一种强大的技术来监测其真菌培养物的菌丝体生长动态,这是控制奶酪制作的重要一步。