sorokinia chllorella的分离、分子鉴定、光营养因子、微营养因子和异养因子的制造

Döndü Yalçin Bingül, Zeliha Demirel, Meltem Conk Dalay
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引用次数: 0

摘要

:使用稀释和倾倒板法从取自伊兹密尔Gumuldur地区的海水样本中分离出微藻。经光镜下形态学鉴定,该种为小球藻。通过分子方法分离微藻DNA,并通过PCR扩增16S和18S rRNA基因区域。通过对基因区域的测序和系统发育评价,确定该微藻为索氏小球藻。采用离心洗涤、抗生素处理、琼脂生长和单细胞分离等不同方法获得异源性sorokinana C。测定了光养索氏囊藻(分别为0.19g L-1和0.78 d-1)、混合营养索氏囊菌(分别为0.31g L-1和1.3 d-1)和异养索氏池藻(分别是0.6g L-1、2.52 d-1)的生物量和比生长速率。研究结果表明,在不同培养条件下,异源性索氏藻的生物量生产力可分为:异养>混养>光养。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chlorella sorokiniana’ nın İzolasyonu, Moleküler Tanılanması, Fototrofik, Miksotrofik Ve Heterotrofik Üretimi
: Microalgae was isolated using dilution and pouring plate method from the sea water sample taken from the Gumuldur region of Izmir. The species was identified as Chlorella sp. through morphologic evaluation under light microscope. Microalgae DNA was isolated through molecular methods and 16S and 18S rRNA gene regions were amplified by means of PCR. As a result of sequencing and phylogenetic evaluation of the gene regions, it was determined that the microalgae was Chlorella sorokiniana . Different methods such as centrifuge washing, antibiotic treatment, growth on agar and single cell isolation used to obtain axenic C. sorokiniana yielded successful results. Biomass and specific growth rate of phototrophic C. sorokiniana (0.19 g L -1 and 0.78 days -1 , respectively), mixotrophic C. sorokiniana (0.31 g L -1 and 1.3 days -1 , respectively) and heterotrophic C. sorokiniana (0.6 g L -1 and 2.52 days -1 , respectively) were determined. According to the findings obtained, the biomass productivity of axenic C. sorokiniana under different culture conditions can be ordered as: heterotrophy > mixotrophy > phototrophy.
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