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歐盟評估一種由內(nèi)切-1,4-β-木聚糖酶和內(nèi)切-1,3(4)-β-葡聚糖酶組成的添加劑作為育肥豬等物種飼料添加劑的授權(quán)更新申請
日期:2024-08-09  來源:食品伙伴網(wǎng)
   食品伙伴網(wǎng)訊  2024年8月8日,歐盟食品安全局EFSA)發(fā)布消息,歐盟食品安全局(EFSA)發(fā)布關(guān)于一種由內(nèi)切-1,4-β-木聚糖酶和內(nèi)切-1,3(4)-β-葡聚糖酶組成的添加劑作為育肥豬、小型育肥豬種和育肥火雞飼料添加劑的授權(quán)更新申請的評估。
 
  據(jù)了解,添加劑中的內(nèi)切-1,4-β-木聚糖酶是由里氏木霉MUCL 49755生產(chǎn)的,內(nèi)切-1,3(4)-β-葡聚糖酶是由里氏木霉MUCL 49754生產(chǎn)的。
 
  經(jīng)過評估,專家小組得出結(jié)論,在建議的使用條件下,該添加劑對目標(biāo)物種、消費(fèi)者和環(huán)境是安全的。在授權(quán)更新的情況下,無需評估添加劑的功效。部分原文報(bào)道如下:
 
  Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the feed additive consisting of endo-1,4-beta-xylanase (produced with Trichoderma reesei MUCL 49755) and endo-1,3(4)-beta-glucanase (produced with T. reesei MUCL 49754) (AveMix® XG 10/AveMix® XG 10 L) for the renewal of its authorisation as zootechnical feed additive for pigs for fattening, minor porcine species for fattening and turkeys for fattening. The applicant declared a change in the carrier material used in AveMix® XG 10 from soybean meal to calcium carbonate + wheat flour or calcium carbonate + sepiolite. The applicant provided evidence that the additive Avemix® XG 10 with calcium carbonate + wheat flour and Avemix® XG 10 L comply with the conditions of the authorisation. The EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) noted that no data were submitted to support compliance of the formulation of Avemix® XG 10 with calcium carbonate + sepiolite with the conditions of the authorisation. The FEEDAP Panel concluded that both forms of the additive remain safe for pigs for fattening, minor porcine species for fattening and turkeys for fattening, consumers and the environment. Regarding the safety for the user, Avemix® XG 10 formulated with calcium carbonate + sepiolite and Avemix® XG 10 L are not irritant to skin and eyes. No conclusions on the irritation potential of Avemix® XG 10 formulated with calcium carbonate + wheat flour could be drawn. The additive in all its formulations is considered a respiratory and skin sensitiser. There was no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.
 
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