کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9604435 | 43625 | 2005 | 12 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Improved mannitol production by a random mutant of Leuconostoc pseudomesenteroides
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کلمات کلیدی
PGIdithiotreitolMDHCDWPTSLeuconostocDTTIPTGEtOHCDMLAB - آزمایشگاهEthanol - اتانولAcetic acid - اسید استیکLactic acid - اسید لاکتیکisopropyl β-D-thiogalactopyranoside - ایزوپروپیل β-D-thiogalactopyranosideHAC - اینجاLactic acid bacteria - باکتریهای اسیدلاکتیکFru - زنFructose - فروکتوز Fructokinase - فروکتوکینازchemically defined medium - ماده شیمیایی تعریف شده استMannitol - مانیتولMannitol dehydrogenase - مانیتول دهیدروژنازFructose metabolism - متابولیسم فروکتوزcell dry weight - وزن خشک سلولیHPLC - کروماتوگرافی مایعی کاراhigh-performance liquid chromatography - کروماتوگرافی مایعی کاراGlu - گلوGlucose - گلوکز
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
بیو مهندسی (مهندسی زیستی)
پیش نمایش صفحه اول مقاله

چکیده انگلیسی
A mutant of Leuconostoc pseudomesenteroides ATCC12291 that was unable to grow on fructose was constructed by chemical mutagenesis. The fructose uptake of this mutant, designated as BPT143, was unaltered and allowed fructose still to be converted into mannitol when glucose was present in the growth medium. The mutant grew and consumed fructose faster than the parent strain when grown in a medium containing both glucose and fructose. The specific activity of fructokinase, the enzyme involved in phosphorylation of fructose to fructose-6-phosphate, was decreased to about 10% of that of the parent strain, and resulted in a reduced leakage of fructose into the phosphoketolase (PK) pathway. The yield of mannitol from fructose was improved from 74 to 86Â mol%. The increased fructose consumption rate and higher mannitol yield of the mutant also resulted in improvement of volumetric mannitol productivity. In addition, isolation and characterization of the wild type L. pseudomesenteroides fructokinase gene (fruK) was performed. DNA sequence analysis of the fruK gene region of BPT143 revealed only one silent mutation which does not explain the highly reduced fructokinase activity of the mutant. The genetic characterization of fruK was completed by analyzing the expression, size and 5â² end of fruK transcripts. Expression data with BPT143, revealing absence of fruK transcripts, was in accordance with the reduced fructokinase activity of the mutant.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Biotechnology - Volume 116, Issue 3, 30 March 2005, Pages 283-294
Journal: Journal of Biotechnology - Volume 116, Issue 3, 30 March 2005, Pages 283-294
نویسندگان
Miia Helanto, Johannes Aarnikunnas, Niklas von Weymarn, Ulla Airaksinen, Airi Palva, Matti Leisola,